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    <title>Recent uciem_cpcem items</title>
    <link>https://escholarship.org/uc/uciem_cpcem/rss</link>
    <description>Recent eScholarship items from Clinical Practice and Cases in Emergency Medicine</description>
    <pubDate>Mon, 2 Nov 2026 13:13:45 +0000</pubDate>
    <item>
      <title>Diagnosing a Fractured Pedunculated Osteochondroma Using Point-of-Care Ultrasound in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/2t1915kk</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; This case report discusses the use of point-of-care ultrasound (POCUS) in the diagnosis of a fractured pedunculated osteochondroma in an 8-year-old boy after minor trauma. Although osteochondromas are the most common benign bone tumors, especially in this age, historically only radiographs have been obtained in the emergency department to diagnose these benign bone tumors.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;An 8-year-old boy reported ongoing pain for 2 months but had an acute onset worsening of his pain after minor trauma to the medial distal right femur. Point-of-care ultrasound was used to diagnose a fractured pedunculated osteochondroma prior to radiographic imaging.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; We demonstrated the practicality and ease of POCUS in assisting with the diagnosis of &amp;nbsp;an osteochondroma and the subtle fracture of the base. Both POCUS and radiographic imaging may be beneficial when used in conjunction for the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2t1915kk</guid>
      <pubDate>Sat, 31 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wilson, Jared</name>
      </author>
      <author>
        <name>Tremwel, Martin</name>
      </author>
      <author>
        <name>Query, Madeline</name>
      </author>
    </item>
    <item>
      <title>Drug-Induced Immune Thrombocytopenia Caused by Sulfamethoxazole-Trimethoprim: A Case Report</title>
      <link>https://escholarship.org/uc/item/6959f45r</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Drug-induced immune thrombocytopenia (DITP) is a rare process in which specific drugs induce antibodies against platelet antigens, resulting in the destruction, consumption, or impaired production of platelets.1,3 Sulfamethoxazole-trimethoprim can result in DITP.2&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; This is a case of a 64-year-old man who developed severe thrombocytopenia after sulfamethoxazole-trimethoprim use. He presented to the emergency department with oral hemorrhagic lesions, mucositis, and petechiae. Laboratory evaluation revealed a low platelet count. Drug-induced immune thrombocytopenia was suspected, and the sulfamethoxazole-trimethoprim was discontinued. The patient’s platelet count responded rapidly after discontinuation of the offending drug and administration of dexamethasone.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights the importance of early recognition of DITP and the avoidance of re-exposure to the causative agent....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6959f45r</guid>
      <pubDate>Fri, 30 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Powell, Alec</name>
      </author>
      <author>
        <name>Weindruch, Louisa</name>
        <uri>https://orcid.org/0000-0002-7573-6077</uri>
      </author>
      <author>
        <name>Thornton, Jonathan</name>
      </author>
    </item>
    <item>
      <title>A 30-Year-Old Man With Rapid Floor-of-Mouth Swelling After Facial Trauma</title>
      <link>https://escholarship.org/uc/item/4t38k2vq</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 30-year-old man presented to the emergency department with severe blunt facial trauma following a fall from height. Examination revealed extensive floor-of-mouth ecchymosis and a large tense sublingual hematoma causing tongue elevation, dysarthria, and swelling mimicking Ludwig’s angina, producing a traumatic pseudo-Ludwig appearance with marked airway crowding. Three-dimensional computed tomography demonstrated severely displaced bilateral mandibular fractures. Owing to pronounced segmental instability with mobile dentoalveolar fragments, temporary interdental bridle wire stabilization was performed in the emergency department. Despite the dramatic anatomical findings, serial airway reassessments confirmed sustained airway stability, permitting delayed definitive open reduction and internal fixation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion:&amp;nbsp;&lt;/strong&gt;Traumatic pseudo-Ludwig angina secondary to bilateral mandibular fractures is an uncommon presentation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4t38k2vq</guid>
      <pubDate>Fri, 30 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Imran, Mohammed Naveeth</name>
        <uri>https://orcid.org/0009-0002-2037-0538</uri>
      </author>
      <author>
        <name>Ravipragasam, Surendar</name>
        <uri>https://orcid.org/0000-0002-7760-0210</uri>
      </author>
      <author>
        <name>Hemanthraj, Shwetha Pujari</name>
        <uri>https://orcid.org/0009-0000-6770-0210</uri>
      </author>
    </item>
    <item>
      <title>Nitrous Oxide “Whippet” Induced Subacute Combined Degeneration of the Spinal Cord: A Case Report</title>
      <link>https://escholarship.org/uc/item/4c34p58q</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Subacute combined degeneration (SCD) is an uncommon neurologic complication of vitamin B12 deficiency characterized by demyelination of the dorsal and lateral columns of the spinal cord, resulting in weakness, paresthesias, sensory deficits, and gait ataxia. Recreational nitrous oxide inhalation has emerged as an important cause of functional vitamin B12 deficiency and may precipitate SCD, particularly in otherwise healthy individuals.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a case of nitrous oxide-associated SCD in a patient who presented to the emergency department with progressive neurologic symptoms. This case illustrates a rare but increasingly recognized complication of recreational nitrous oxide use.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Nitrous oxide-induced SCD should be considered in patients presenting with subacute weakness, paresthesia, and ataxia, particularly when there is a history of recreational inhalant use. Early recognition...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4c34p58q</guid>
      <pubDate>Fri, 30 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kern, Joshua</name>
        <uri>https://orcid.org/0000-0003-0406-5234</uri>
      </author>
      <author>
        <name>Shanks, Carolyn</name>
      </author>
    </item>
    <item>
      <title>Bougie-Assisted Blakemore Tube Insertion: A Case Series</title>
      <link>https://escholarship.org/uc/item/2h11t4mb</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Variceal hemorrhage is a life-threatening complication of portal hypertension that requires rapid hemorrhage control. Gastroesophageal balloon tamponade devices are effective temporizing measures when endoscopic or definitive therapies are delayed or unsuccessful, but placement can be technically challenging during active bleeding. A bougie-assisted technique has been proposed to improve ease and success of placement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series:&lt;/strong&gt; We describe three patients with cirrhosis and varices who presented with massive upper gastrointestinal bleeding and hemorrhagic shock. All received standard medical therapy and required escalation due to ongoing bleeding. In each case, a Sengstaken-Blakemore tube was placed using a bougie tracheal tube introducer as a semirigid stylet. The device was advanced under laryngoscopy through the esophagus and into the stomach without procedural complications. Hemostasis was achieved in all cases following...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2h11t4mb</guid>
      <pubDate>Fri, 30 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gardner, Shane</name>
      </author>
      <author>
        <name>Tachney, Andrew</name>
      </author>
      <author>
        <name>Cobbs, Adele</name>
      </author>
      <author>
        <name>Putman, Margaret</name>
      </author>
      <author>
        <name>Hase, Travis</name>
      </author>
    </item>
    <item>
      <title>Use of Point-of-Care Ultrasound to Confirm and Manage a Morel-Lavallée Lesion in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/0t31n6jt</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Morel-Lavallée lesions are closed, soft tissue degloving injuries that occur when shearing forces separate the subcutaneous tissue from the underlying fascia. This creates a potential space for hemolymphatic fluid accumulation. Morel-Lavallée lesions are frequently under-reported and often misdiagnosed as hematomas or abscesses, leading to potential mismanagement. While magnetic resonance imaging (MRI) is considered the gold standard for diagnosis, point-of-care ultrasound (POCUS) has been shown to be an effective adjunct that can rapidly confirm sonographic features consistent with Morel-Lavallée lesions, support MRI-established findings, and guide procedural intervention in the emergency department (ED) setting.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We describe a 20-year-old woman presenting to the ED with persistent right-sided hip pain two months after a pedestrian–motor vehicle collision. Initially misdiagnosed as a hematoma, an outpatient...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0t31n6jt</guid>
      <pubDate>Fri, 30 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shanbhag, Siddharth</name>
      </author>
      <author>
        <name>Kurzweil, Ami</name>
      </author>
    </item>
    <item>
      <title>Emergency Department Use of Genicular Nerve Block for Sickle Cell Pain Crisis: A Case Report</title>
      <link>https://escholarship.org/uc/item/9xr5x36m</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Acute pain crises are a common emergency department presentation in patients with sickle cell disease. Pain management typically relies on multimodal analgesia, with opioids often playing a central role. We propose incorporating regional anesthesia techniques into the pain management regimen.&lt;/p&gt;
&lt;p&gt;&lt;br&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present a case of a young patient with sickle cell disease experiencing an acute pain crisis with severe knee pain. A genicular nerve block was performed, resulting in significant pain reduction in the affected knee.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;br&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Regional anesthesia, including isolated nerve blocks, may be safe and effective as part of a multimodal pain approach for patients suffering from acute pain crises due to sickle cell disease. This may help reduce the need for opioid or other sedating pain medications, as well as the inherent risks associated with increasing doses, such as respiratory depression.&amp;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xr5x36m</guid>
      <pubDate>Mon, 26 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Beranek, Rosemary</name>
      </author>
      <author>
        <name>Musial, Hayley</name>
      </author>
      <author>
        <name>Parsons-Moss, Daniel</name>
      </author>
      <author>
        <name>Dreyfuss, Andrea</name>
      </author>
    </item>
    <item>
      <title>59-year-old Woman with Acute Blindness</title>
      <link>https://escholarship.org/uc/item/9nc131tb</link>
      <description>&lt;p&gt;When a patient with acute blindness presents to the emergency department (ED), the evaluation typically suggests one of the “can’t miss” diagnoses ingrained in emergency physicians during training. How does the differential change when the patient’s presentation does not neatly reveal an expected pathology? A 59-year-old woman presented to the ED with acute binocular blindness in the setting of three days of a flu-like illness. This case offers a practical approach to opening the lens on the presentation of acute blindness.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9nc131tb</guid>
      <pubDate>Mon, 26 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Contillo, Nicolas</name>
      </author>
      <author>
        <name>Sibel, Michael</name>
        <uri>https://orcid.org/0009-0008-5273-4619</uri>
      </author>
      <author>
        <name>Bontempo, Laura J</name>
        <uri>https://orcid.org/0000-0002-1961-6003</uri>
      </author>
      <author>
        <name>Gatz, John David</name>
        <uri>https://orcid.org/0000-0002-3380-2419</uri>
      </author>
    </item>
    <item>
      <title>Retrocaval Ureter Diagnosed Following Point-of-Care Ultrasound Detection of Hydronephrosis: A Case Report</title>
      <link>https://escholarship.org/uc/item/7xd4v36t</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Retrocaval ureter (RCU) is a rare congenital anomaly resulting from abnormal development of the inferior vena cava, leading to ureteral obstruction and hydronephrosis. Patients often present with nonspecific symptoms, making diagnosis challenging. Point-of-care ultrasound (POCUS) is frequently used in the emergency department (ED) to evaluate abdominal pain and may identify clinically important abnormalities requiring further investigation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 30-year-old woman presented to the ED with a two-day history of nonspecific abdominal pain. Physical examination was notable only for mild epigastric tenderness. Abdominal POCUS performed by the emergency physician demonstrated moderate right-sided hydronephrosis. The patient had no urinary symptoms and normal renal function. Follow-up renal ultrasound confirmed hydronephrosis and proximal hydroureter without nephrolithiasis. Contrast-enhanced computed tomography subsequently...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7xd4v36t</guid>
      <pubDate>Mon, 26 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Marzook, Noah</name>
        <uri>https://orcid.org/0000-0001-9733-643X</uri>
      </author>
      <author>
        <name>Alhabboubi, Mostafa</name>
        <uri>https://orcid.org/0000-0002-8741-8877</uri>
      </author>
      <author>
        <name>Koshak, Ahmad</name>
      </author>
      <author>
        <name>Basnawi, Abdullah</name>
      </author>
      <author>
        <name>Ajabnoor, Yasser</name>
      </author>
      <author>
        <name>Albadr, Suha</name>
      </author>
    </item>
    <item>
      <title>Carotid Artery Dissection After Cervical Traction Device Use: A Case Report</title>
      <link>https://escholarship.org/uc/item/1v58v6b7</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Internal carotid artery (ICA) dissection is a time-sensitive vascular emergency that may present with subtle findings, most notably painful Horner syndrome. Mechanical stress to the cervical vasculature is a recognized trigger for this condition.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a 56-year-old man who developed ipsilateral ptosis, miosis, and head and neck pain after using a home cervical traction device. Computed tomography angiography showed focal critical stenosis of the distal cervical left ICA consistent with dissection, along with a contralateral pseudoaneurysm suggesting prior injury. He was treated with dual antiplatelet therapy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights a potential association between cervical traction device use and carotid dissection and underscores the importance of recognizing painful Horner syndrome and bilateral carotid pathology, while prompting clinicians to specifically inquire about...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1v58v6b7</guid>
      <pubDate>Mon, 26 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Samadian, Kian D.</name>
        <uri>https://orcid.org/0009-0008-5289-9325</uri>
      </author>
      <author>
        <name>Nothnagle, Maureen K.</name>
      </author>
      <author>
        <name>Mostaghimi, Sina M.</name>
      </author>
      <author>
        <name>Alhoyek, Sandra</name>
      </author>
      <author>
        <name>Babar, Rehmat</name>
      </author>
      <author>
        <name>He, Shuhan</name>
      </author>
    </item>
    <item>
      <title>Parainfectious Urticarial Rash in a Young Female with Epstein-Barr Virus Infection: A Case Report</title>
      <link>https://escholarship.org/uc/item/8wb0r6qg</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Urticarial rash is a common condition but can present atypically, making it difficult to clinically diagnose. Thorough assessment with awareness and exclusion of differentials is crucial for definitive treatment.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; This is a case of a 23-year-old woman who presented with signs and symptoms suggestive of streptococcal pharyngitis and was treated with clarithromycin by primary care. Two weeks later, the patient was referred to the emergency department for malaise and an acute, rapidly progressing pruritic rash. Further evaluation revealed an Epstein-Barr virus (EBV) infection.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights the differential diagnoses and diagnostic reasoning required for a patient with a rash and concurrent respiratory symptoms. Differential considerations include viral exanthem, delayed drug-induced reaction, EBV-associated antibiotic rash, scarlet fever, and urticarial vasculitis....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8wb0r6qg</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Huang, XinYao Oliver</name>
        <uri>https://orcid.org/0009-0001-4129-4688</uri>
      </author>
      <author>
        <name>Yap, Andrea</name>
      </author>
      <author>
        <name>Toh, Dawn</name>
      </author>
      <author>
        <name>Lim Hoon Chin, Steven</name>
      </author>
    </item>
    <item>
      <title>Delayed Revascularization in Rural Acute STEMI Patient on Direct Oral Anticoagulation: A Case Report</title>
      <link>https://escholarship.org/uc/item/76z871q6</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acute ST-elevated myocardial infarction (STEMI) is a medical emergency requiring timely revascularization to preserve myocardial injury. Rural populations often experience delays in treatment leading to increased risk of complications and mortality. Emergent treatment of STEMI in a patient on long-term direct oral anticoagulation facing delays to revascularization is a complex scenario for rural physicians.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 55-year-old male presented to the emergency department in rural Alaska and was diagnosed with acute inferior STEMI. The patient’s history was notable for pulmonary embolism with long-term direct oral anticoagulation. Thrombolytic therapy was not recommended and prompt revascularization via percutaneous coronary intervention (PCI) was needed; however, the nearest PCI-capable hospital was hundreds of miles away, increasing the risk of ischemic cardiomyopathy and death. The patient achieved revascularization...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/76z871q6</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Roetman, Seth</name>
        <uri>https://orcid.org/0009-0007-0895-2646</uri>
      </author>
      <author>
        <name>Brandecker, Gary</name>
      </author>
    </item>
    <item>
      <title>From Frenulum Tear to Transfusion—An Unexpected Diagnosis of Hemophilia in a Toddler: A Case Report</title>
      <link>https://escholarship.org/uc/item/5xj546w6</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Labial frenulum tears in infants are commonly associated with minor trauma but may raise concern for nonaccidental injury. These injuries are typically benign and self-limiting; however, persistent or excessive bleeding should prompt evaluation for an underlying bleeding disorder. Hemophilia A is an X-linked factor VIII deficiency with clinical symptoms that vary based on the level of severity.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A previously healthy 14-month-old male presented to the pediatric emergency department three times within 10 days for persistent bleeding from a superior labial frenulum tear sustained after minor trauma. Initial examination was reassuring, and he was discharged without laboratory evaluation. On repeat presentation, he was found to have normocytic anemia and isolated prolonged activated partial thromboplastin time. Despite topical and oral antifibrinolytic therapy, he returned with worsening anemia, melena, hematemesis,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xj546w6</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Busta, Saxony</name>
        <uri>https://orcid.org/0009-0004-3706-4857</uri>
      </author>
      <author>
        <name>Piroutek, Mary Jane</name>
      </author>
    </item>
    <item>
      <title>Spontaneous Cardiac Tamponade in a Patient with Severe Hemophilia A: A Case Report</title>
      <link>https://escholarship.org/uc/item/4h87d646</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Hemophilia A is an X-linked recessive bleeding disorder characterized by deficiency of factor VIII. The clinical features of this disease are hemorrhage and can be life-threatening when major organ systems are involved.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 13-year-old boy with severe hemophilia A and factor VIII inhibitors who presented with fever and septic arthritis, later developing refractory shock with tachyarrhythmia. Despite initial suspicion of sepsis-related myocarditis, point-of-care ultrasound (POCUS) revealed massive hemorrhagic pericardial effusion with tamponade physiology. Recombinant factor VIIa was transfused as hemostatic rescue therapy; the patient was subsequently started on fresh frozen plasma and emicizumab. Ultrasound-guided pericardiocentesis resulted in rapid hemodynamic recovery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights the importance of considering obstructive shock in unstable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4h87d646</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Singh, Teenu</name>
        <uri>https://orcid.org/0009-0006-2735-3764</uri>
      </author>
      <author>
        <name>Wali, Sachin</name>
        <uri>https://orcid.org/0009-0009-7890-8944</uri>
      </author>
      <author>
        <name>Gutte, Shreyas</name>
      </author>
      <author>
        <name>Azim, Afzal</name>
      </author>
      <author>
        <name>Poddar, Banani</name>
      </author>
    </item>
    <item>
      <title>Inguinal Bladder Herniation in the Emergency Department: A Report of Two Cases</title>
      <link>https://escholarship.org/uc/item/1nf4q0b6</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Inguinal bladder herniation is a rare subtype of inguinal hernia in which the urinary bladder protrudes into the inguinal canal. It is often asymptomatic but can present with a range of clinical severity in the emergency department (ED).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present a case report of two patients with inguinal bladder hernias. The first case describes a stable patient with bladder herniation without urinary obstruction, successfully managed with outpatient follow-up. The second case illustrates a more severe presentation with bladder involvement causing bilateral hydroureteronephrosis, requiring admission after failed reduction. This patient subsequently re-presented with urosepsis and developed multiple complications, including bacteremia and infective endocarditis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Inguinal bladder herniation can present with a wide clinical spectrum in the ED. Early recognition, appropriate imaging, and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1nf4q0b6</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chan, Bill</name>
      </author>
      <author>
        <name>Sloane, Skyler</name>
      </author>
      <author>
        <name>Campbell, Colleen</name>
      </author>
      <author>
        <name>Ly, Binh</name>
      </author>
      <author>
        <name>Subramony, Rachna</name>
        <uri>https://orcid.org/0000-0002-1340-2231</uri>
      </author>
    </item>
    <item>
      <title>Before Hyperemesis Gravidarum Is Blamed for Thiamine Deficiency, Alternative Causes Should Be Ruled Out</title>
      <link>https://escholarship.org/uc/item/0ph557bs</link>
      <description>&lt;p&gt;n/a&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0ph557bs</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Finsterer, Josef</name>
      </author>
    </item>
    <item>
      <title>Acute Myocardial Infarction Following Tenecteplase: A Case Report of Complex Dual Pathology</title>
      <link>https://escholarship.org/uc/item/0fz1n4gw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acute ischemic stroke is a leading cause of morbidity and mortality, with tenecteplase being a cornerstone of acute management. While tenecteplase carries a known risk of bleeding, major thrombotic events such as acute myocardial infarction (AMI) after stroke reperfusion are less commonly described.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present the case of a 67-year-old man who presented with acute stroke symptoms. After ruling out intracranial hemorrhage and managing blood pressure, he received tenecteplase, and all neurological deficits resolved. Soon after, he developed acute chest pain, and his repeat electrocardiogram confirmed a ST-elevation myocardial infarction. He underwent emergent cardiac catheterization, revealing 100% occlusion of the left circumflex artery, which was successfully revascularized with thrombectomy and angioplasty. Intravascular ultrasound further supported the presence of embolic phenomenon. Pathology of the retrieved...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0fz1n4gw</guid>
      <pubDate>Tue, 20 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Howell, Devin</name>
        <uri>https://orcid.org/0000-0002-3643-1051</uri>
      </author>
      <author>
        <name>Ramirez Damera, Ramses</name>
        <uri>https://orcid.org/0000-0002-9356-8433</uri>
      </author>
      <author>
        <name>Rao, Gaurav</name>
        <uri>https://orcid.org/0000-0002-6266-1184</uri>
      </author>
    </item>
    <item>
      <title>Focal Hepatic Hot Spot Sign Mimicking Active Extravasation on CT Angiography in Superior Vena Cava Syndrome: A Case Report</title>
      <link>https://escholarship.org/uc/item/7r7901z3</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Caused by portosystemic venous shunting, the focal hepatic hot spot sign (or hot quadrate sign) is a radiologic finding most commonly associated with superior vena cava (SVC) obstruction. On contrast-enhanced imaging, this finding may mimic active hepatic extravasation or focal hepatic pathology, posing a diagnostic challenge in the emergency department (ED).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a case of a 70-year-old man with progressive cognitive decline and hypoxemic respiratory failure requiring intubation. Computed tomography (CT) angiography of the chest demonstrated a focal area of intense contrast enhancement in the left hepatic lobe, initially concerning for active extravasation. Further review of the imaging revealed a right upper lobe lung mass and a large mediastinal mass causing high-grade SVC stenosis. The hepatic finding was subsequently identified by the reading radiologist as a focal hepatic hot spot sign representing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7r7901z3</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wilkerson, R. Gentry</name>
        <uri>https://orcid.org/0000-0001-8301-4421</uri>
      </author>
      <author>
        <name>Brecher, Vanesa</name>
      </author>
    </item>
    <item>
      <title>Atypical Emergency Department Presentation of Acute Motor and Sensory Axonal Neuropathy: A Case Report</title>
      <link>https://escholarship.org/uc/item/74n0k0dh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acute motor and sensory axonal neuropathy is a rare, severe axonal variant of Guillain–Barré syndrome characterized by rapidly progressive motor and sensory dysfunction. Early recognition in the emergency department (ED) is challenging because patients may initially present with subtle neurologic findings, preserved reflexes, and normal cerebrospinal fluid (CSF) studies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 29-year-old woman with a history of generalized anxiety disorder presented to the ED with progressive distal numbness and mild weakness, with weakness being her chief complaint. Neurologic examination demonstrated preserved reflexes without focal deficits, and she was noted to be anxious. Given the reassuring examination, the patient was discharged with strict return precautions, including instructions to seek immediate reevaluation for worsening weakness, numbness, or progression of neurologic symptoms. She returned 48 hours later...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/74n0k0dh</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kabir, Shadman</name>
        <uri>https://orcid.org/0009-0000-5822-5649</uri>
      </author>
      <author>
        <name>Rahman, Austin</name>
      </author>
      <author>
        <name>Konopack, Sitha</name>
      </author>
    </item>
    <item>
      <title>Spontaneous Spinal Epidural Hematoma as a Manifestation of Hypertensive Emergency: A Case Report</title>
      <link>https://escholarship.org/uc/item/5st4v840</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Uncontrolled hypertension is frequently evaluated in the emergency department (ED), with the goal of identifying those patients with hypertensive emergencies. Spontaneous spinal epidural hematoma is rare and not considered a typical manifestation of hypertensive emergency.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 31-year-old man presenting to the ED with chest pain and hypertension subsequently developed lower extremity neurologic deficits and was diagnosed with a spontaneous spinal epidural hematoma. After thorough testing, no other risk factors for this medical condition were identified, and the hemorrhage was attributed to hypertensive emergency.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Spontaneous spinal epidural hematoma is a rare complication of hypertensive emergency and should be considered when evaluating patients with hypertension, back pain, and neurologic deficits.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5st4v840</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Laird, Kelly</name>
        <uri>https://orcid.org/0009-0001-9834-2337</uri>
      </author>
      <author>
        <name>Sell, Jordan</name>
      </author>
      <author>
        <name>England, Peter</name>
      </author>
      <author>
        <name>Montas, Sacha</name>
      </author>
      <author>
        <name>Walsh, Kevin</name>
      </author>
      <author>
        <name>Harvey, Carrie</name>
      </author>
    </item>
    <item>
      <title>Partial Segmental Thrombosis of the Corpus Cavernosum Following Valsalva Maneuver: A Case Report</title>
      <link>https://escholarship.org/uc/item/4h3020pn</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Partial segmental thrombosis of the corpus cavernosum is a rare vascular condition that may present with nonspecific groin or pelvic pain and mimic more common surgical or urologic emergencies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 33-year-old man presented to the emergency department with acute left-sided groin and pelvic pain after straining during defecation. Initial history and evaluation raised concern for incarcerated inguinal hernia, epididymo-orchitis, renal colic, lymphadenopathy, and soft tissue infection. Computed tomography demonstrated asymmetric enlargement of the left corpus cavernosum, while penile ultrasound showed diminished cavernosal flow. Magnetic resonance imaging confirmed segmental thrombosis of the left corpus cavernosum. The patient was treated conservatively with rivaroxaban and analgesia, resulting in symptomatic improvement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Partial segmental thrombosis of the corpus cavernosum...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4h3020pn</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Konopack, Sitha</name>
      </author>
      <author>
        <name>Diaz, Jessica</name>
      </author>
    </item>
    <item>
      <title>Behavioral Trigger Identification in Recurrent Postpartum Chest Pain After Negative Cardiopulmonary Evaluation: A Case Report</title>
      <link>https://escholarship.org/uc/item/49r2f8bj</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Recurrent chest pain in postpartum patients frequently results in repeated emergency department (ED) visits despite negative cardiopulmonary investigations, creating diagnostic uncertainty and increasing healthcare resource utilization. We report a case highlighting the value of a structured postexclusion assessment to identify clinically relevant behavioral triggers after life-threatening causes have been excluded.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 33-year-old woman, six weeks postpartum, presented repeatedly with nocturnal chest pain, palpitations, and dyspnea. Serial electrocardiograms, cardiac biomarkers, chest imaging, and transthoracic echocardiography were consistently normal, excluding acute cardiopulmonary pathology. Careful reassessment of symptom chronology and behavioral history identified a reproducible temporal association between symptom onset and nocturnal binge-eating episodes. Following outpatient psychiatric and clinical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/49r2f8bj</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shrivastav, Aditya S.</name>
        <uri>https://orcid.org/0009-0007-6319-581X</uri>
      </author>
      <author>
        <name>Tivaskar, Suhas</name>
      </author>
      <author>
        <name>Luharia, Anurag</name>
      </author>
      <author>
        <name>Mishra, Gaurav</name>
      </author>
    </item>
    <item>
      <title>Transient Electrocardiographic Changes in Anaphylaxis Mimicking Acute Coronary Syndrome: A Case Series</title>
      <link>https://escholarship.org/uc/item/3vr247bx</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Anaphylaxis is a life-threatening emergency that can involve significant cardiovascular manifestations. Transient electrocardiographic (ECG) changes during anaphylaxis and following epinephrine administration may closely mimic acute coronary syndrome, creating a diagnostic dilemma in the emergency department (ED). Failure to recognize these reversible patterns can result in delayed anaphylaxis treatment or unnecessary activation of invasive cardiac pathways.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series:&lt;/strong&gt; We report a case series of three adult patients presenting to the ED with anaphylaxis who developed alarming ECG changes, including ST-segment elevation, ST-segment depression, and hyperacute T waves. One patient demonstrated transient ECG changes temporally related to intramuscular epinephrine administration, while two patients exhibited features suggestive of hypersensitivity-associated coronary vasospasm or thrombosis manifesting as ECG changes. In all...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3vr247bx</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>S, Hari Ganesh</name>
      </author>
      <author>
        <name>T, Amrithanand V</name>
        <uri>https://orcid.org/0000-0002-6410-2896</uri>
      </author>
      <author>
        <name>B G, Kowsthubha</name>
        <uri>https://orcid.org/0009-0006-7909-7248</uri>
      </author>
    </item>
    <item>
      <title>Bedside Sonography Brings the Weiss Ring into Focus: Rapid Diagnosis of Posterior Vitreous Detachment</title>
      <link>https://escholarship.org/uc/item/3r13x5c2</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation:&lt;/strong&gt; A 51-year-old woman presented to the emergency department with blurred vision and a large, dark floater in her right eye. Point-of-care ultrasound (POCUS) revealed a Weiss ring, strongly suggesting a diagnosis of a posterior vitreous detachment.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion:&lt;/strong&gt; Identifying a Weiss ring with POCUS may be a reasonable and easier alternative for emergency clinicians when used in conjunction with a slit-lamp examination and may aid in timely ophthalmologic management of posterior vitreous detachments.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3r13x5c2</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Betcher, Joseph</name>
      </author>
      <author>
        <name>Shields, Matthew</name>
        <uri>https://orcid.org/0009-0008-8341-2639</uri>
      </author>
      <author>
        <name>Busch, Dakota</name>
        <uri>https://orcid.org/0009-0009-0137-450X</uri>
      </author>
    </item>
    <item>
      <title>Hemopericardium After Cardiopulmonary Resuscitation—Bedside Drainage with a Triple-Lumen Catheter: A Case Report</title>
      <link>https://escholarship.org/uc/item/3q20v1r0</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Hemopericardium from chest compression-related cardiac injury is an underrecognized complication of cardiopulmonary resuscitation, with bleeding risk amplified in anticoagulated patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 66-year-old man on apixaban and hemodialysis presented in cardiac arrest. Post resuscitation ultrasound revealed pericardial tamponade. With no pericardiocentesis kit available, a seven French triple-lumen central venous catheter was placed under ultrasound guidance via a subxiphoid approach. Approximately one liter of bloody fluid was drained; the patient died within 24 hours.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Hemopericardium is an underrecognized complication of resuscitation in anticoagulated patients. A triple-lumen central venous catheter offers a familiar bedside drainage alternative when a commercial kit is unavailable.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3q20v1r0</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gagliardi, Michael</name>
      </author>
      <author>
        <name>Luu, Melissa</name>
      </author>
      <author>
        <name>Weick, Rose-Ann</name>
      </author>
      <author>
        <name>White, Rebecca</name>
        <uri>https://orcid.org/0009-0004-8810-613X</uri>
      </author>
      <author>
        <name>Abboud, Mohammad T.</name>
        <uri>https://orcid.org/0009-0000-3393-2398</uri>
      </author>
    </item>
    <item>
      <title>A Rare Presentation of Pneumococcal Meningitis with Acute Bilateral Vision Loss: A Case Report</title>
      <link>https://escholarship.org/uc/item/1895v1gz</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Bacterial meningitis affects about 1.2 million people worldwide each year. Streptococcus pneumoniae is responsible for the majority of cases of bacterial meningitis in the United States and Europe, with visual impairment seen in 6.3% of patients. The etiology of acute vision loss in the setting of bacterial meningitis remains wide-ranging, most often occurring in the setting of endogenous endophthalmitis, optic neuropathy, and cortical blindness. Retinal necrosis is rare, and typically associated with viral meningitis, but has not been reported in bacterial meningitis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case report:&lt;/strong&gt; A 66-year-old man with headache, malaise, and intermittent blurry vision, initially diagnosed with viral upper respiratory infection and presumed trigeminal neuralgia, presented to the emergency department with altered mental status, meningismus, and progressive bilateral vision loss. He was diagnosed with bacterial meningitis, and subsequent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1895v1gz</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Anderson, Adam</name>
      </author>
      <author>
        <name>Piszker, Alexander</name>
      </author>
      <author>
        <name>Applebach, Eric</name>
      </author>
      <author>
        <name>Mitchell, Reid</name>
      </author>
      <author>
        <name>Jeng, Aji Yagou</name>
      </author>
    </item>
    <item>
      <title>Cauda Equina Syndrome Secondary to Seizure-Induced Spinal Fracture During Hyperbaric Oxygen Therapy: A Case Report</title>
      <link>https://escholarship.org/uc/item/0901841h</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Hyperbaric oxygen therapy carries a risk of central nervous system oxygen toxicity, which can result in seizures. Seizure-induced spinal fractures are uncommon complications that occur during generalized convulsive activity. While often benign, lumbar vertebral body burst fractures may result in cauda equina syndrome. Additionally, patients with beta-thalassemia may have decreased bone mineral density due to ineffective erythropoiesis and bone marrow expansion increasing the risk for pathologic and traumatic fractures.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 35-year-old man with beta-thalassemia major presented to the emergency department after a witnessed, first-time generalized tonic-clonic seizure during hyperbaric oxygen therapy for chronic venous ulcers. Initial evaluation revealed severe low back pain and midline lumbar tenderness. Computed tomography revealed an acute third lumbar vertebra (L3) burst fracture with retropulsion. The patient...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0901841h</guid>
      <pubDate>Tue, 13 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Aloise, Daniel</name>
      </author>
      <author>
        <name>Nash, Joel</name>
      </author>
      <author>
        <name>Alfred, Gregory</name>
      </author>
      <author>
        <name>Iqbal, Rahib</name>
      </author>
      <author>
        <name>Boccio, Eric</name>
      </author>
    </item>
    <item>
      <title>Type I Choledochal Cyst in a Three-Year-Old with Recurrent Vomiting and Pancreatitis: A Case Report</title>
      <link>https://escholarship.org/uc/item/58g60930</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Choledochal cysts are rare congenital dilatations of the biliary tree that may present with nonspecific gastrointestinal symptoms in children, posing diagnostic challenges.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a 3-year-old girl who presented with recurrent vomiting and abdominal pain. Initial laboratory testing revealed a mildly elevated lipase. An abdominal ultrasound demonstrated a pancreatic cyst; the patient was discharged with outpatient follow-up. She returned with worsening symptoms and a markedly elevated lipase of 2,247 U/L (reference range, &amp;lt; 160 U/L). Computed tomography subsequently revealed a type I choledochal cyst. She underwent operative resection with an uncomplicated postoperative course.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Persistent gastrointestinal symptoms with uptrending lipase in children should prompt consideration of hepatobiliary etiologies. Choledochal cysts may be missed on initial presentation as...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/58g60930</guid>
      <pubDate>Wed, 7 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>DiPrinzio, Dominic</name>
      </author>
      <author>
        <name>Del Mar, Rance</name>
      </author>
    </item>
    <item>
      <title>Status Epilepticus in a Patient Prescribed Theophylline: A Case Report</title>
      <link>https://escholarship.org/uc/item/9962x8nm</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Seizures are a frequent reason for emergency department (ED) evaluation, and new-onset events carry a wide differential in which medication toxicity can be overlooked. Toxicity from seldomly prescribed drugs, such as theophylline, can be particularly challenging to recognize because they can cause nonspecific adverse effects, including palpitations, nausea, vomiting, and seizures. Although theophylline use was widespread in the 1980s, current prescribing patterns are unknown. Nevertheless, theophylline toxicity continues to result in ED visits and poison center calls. Because adverse effects may be acute or chronic, identifying theophylline toxicity remains difficult.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;br&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 74-year-old woman presented to the ED with status epilepticus. After thorough history and extensive medical work-up, medication toxicity was suspected as the cause of her seizures. Upon further investigation, the patient was found...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9962x8nm</guid>
      <pubDate>Tue, 6 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Coyle, Cynthia</name>
      </author>
      <author>
        <name>Samones, Emmelyn J.</name>
      </author>
      <author>
        <name>Phan, Tammy</name>
      </author>
      <author>
        <name>Guptill, Mindi</name>
      </author>
    </item>
    <item>
      <title>Intracardiac Placement of Needle Thoracostomy Catheter by Paramedics Due to Anatomic Variation: A Case Report</title>
      <link>https://escholarship.org/uc/item/7gw455sf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Needle thoracostomy is the only procedure in the United States for paramedic treatment of suspected tension pneumothorax within the most recent emergency medical services (EMS) national scope of practice model. We present a rare complication of an out-of-hospital left needle thoracostomy performed by paramedics after intracardiac placement of the catheter. The patient’s imaging studies in the receiving emergency department (ED) confirmed that the needle thoracostomy insertion location was correct, but the catheter entered the heart due to the patient’s existing atypical anatomy.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 64-year-old unrestrained male driver in a roll-over motor vehicle accident was found in respiratory distress with difficulty auscultating left-sided lung sounds, left chest wall pain on palpation, and confusion. The first-arriving paramedics performed a left needle thoracostomy for suspected tension pneumothorax in advance of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7gw455sf</guid>
      <pubDate>Tue, 6 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Strain, Brian</name>
      </author>
      <author>
        <name>Meeker, Scott</name>
      </author>
      <author>
        <name>Dukes, W. Seth</name>
      </author>
      <author>
        <name>Savino, Paul Brian</name>
      </author>
    </item>
    <item>
      <title>Case Report of Orthopedic Screw Migration Presenting as Abdominal Pain in the Emergency Department</title>
      <link>https://escholarship.org/uc/item/3kt0h6nq</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Hip fractures are a concern in older adults, with incidence expected to rise as the population ages. Despite advances in surgical technique and hardware design, complications remain, influenced by patient factors and surgical choices. Rarely, hardware migration into the pelvis occurs, which poses serious risks. In the emergency setting, abdominal pain is a common complaint, and when evaluating patients with complex histories or prior orthopedic surgeries, clinicians must maintain a broad differential. This case details the discovery of a medially displaced hip screw into the pelvis as the cause of abdominal pain in a patient in the emergency department (ED).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 44-year-old female with end stage renal disease on hemodialysis, anemia, and osteoporosis presented to the ED with sudden-onset, bilateral lower quadrant abdominal pain, vomiting, and diarrhea. The patient reported undergoing left hip open reduction and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3kt0h6nq</guid>
      <pubDate>Tue, 6 Oct 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jones, Eric</name>
      </author>
      <author>
        <name>Khan, Marium</name>
      </author>
      <author>
        <name>Samones, Emmelyn J.</name>
      </author>
      <author>
        <name>Savino, Paul Brian</name>
      </author>
    </item>
    <item>
      <title>Polysubstance-Induced Vasoplegia Managed with Venoarterial Extracorporeal Membrane Oxygenation: A Case Report</title>
      <link>https://escholarship.org/uc/item/83z4d341</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;While the use of venoarterial extracorporeal membrane oxygenation (VA-ECMO) becomes increasingly commonplace in overdose, questions about its role in various shock states remain. The application of VA-ECMO with impaired myocardial function is well established, and use in cardiogenic shock precipitated by poisoning has continued to increase. In poison-induced vasoplegia with preserved myocardial function, the role of VA-ECMO remains undefined. Many atypical antipsychotic and antidepressant agents are known to cause mild hypotension via alpha-1 adrenergic blockade. Intravenous fluids and vasopressors alone are generally effective for single-substance ingestions. In the setting of polysubstance intoxication, synergism leading to bradycardia and refractory vasoplegia refractory to conventional therapies may result, prompting consideration for extracorporeal support.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 71-year-old woman presented to the emergency...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/83z4d341</guid>
      <pubDate>Sat, 26 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Bleifuss, William J.</name>
        <uri>https://orcid.org/0009-0006-6260-2500</uri>
      </author>
      <author>
        <name>Robinson, Aaron E.</name>
      </author>
      <author>
        <name>Heather, Beth M.</name>
      </author>
      <author>
        <name>Brown, Hannah M.</name>
        <uri>https://orcid.org/0000-0001-6513-7356</uri>
      </author>
      <author>
        <name>Floden, Tyler G.</name>
      </author>
      <author>
        <name>Cole, Jon B.</name>
      </author>
    </item>
    <item>
      <title>Idiopathic Left Anterior Fascicular Ventricular Tachycardia in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/60s2b7xc</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Idiopathic fascicular ventricular tachycardia is a rare form of ventricular tachycardia that is commonly seen in young, otherwise healthy individuals without structural heart disease. This rhythm can be difficult to distinguish from other forms of tachyarrhythmia, including supraventricular tachycardia, yet acute pharmacologic management of this condition varies significantly from more common forms.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We describe a 42-year-old woman with no cardiac history who presented with palpitations and lightheadedness. She was found to be in a hemodynamically stable, wide-complex tachycardia. Given no prior cardiac history, supraventricular tachycardia with aberrancy was initially considered as a leading diagnosis; however, a trial of adenosine and lidocaine was ineffective. Her electrocardiogram revealed a regular wide complex tachycardia at 262 beats per minute with a right bundle branch block morphology and right axis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/60s2b7xc</guid>
      <pubDate>Sat, 26 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kofman, Rochelle</name>
      </author>
      <author>
        <name>O'Hare, Connor</name>
      </author>
      <author>
        <name>Querin, Lauren B.</name>
      </author>
    </item>
    <item>
      <title>Mechanical Small Bowel Obstruction Secondary to Deflated and Migrated Intragastric Balloon</title>
      <link>https://escholarship.org/uc/item/4179s4n2</link>
      <description>&lt;p&gt;&lt;strong&gt;Case presentation:&lt;/strong&gt; A 29-year-old woman presented to the emergency department three months after intragastric balloon placement with nausea, vomiting, constipation, and abdominal pain. Computed tomography (CT) demonstrated spontaneous deflation and migration of the device into the small bowel with resultant mechanical small bowel obstruction. The patient was managed conservatively with bowel rest, intravenous fluids, electrolyte repletion, and nasogastric decompression. Repeat CT on hospital day 2 confirmed distal migration of the balloon into the descending colon with interval decompression of the small bowel. On hospital day 3, the patient reported spontaneous passage of the balloon per rectum with complete resolution of symptoms.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion:&lt;/strong&gt; Spontaneous deflation and distal migration of an intragastric balloon causing small bowel obstruction is a rare but potentially life-threatening complication. Most reported cases require surgical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4179s4n2</guid>
      <pubDate>Sat, 26 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moas, Luis</name>
      </author>
      <author>
        <name>Feraud, Arturo</name>
      </author>
      <author>
        <name>Baksh, Aliyah</name>
      </author>
      <author>
        <name>Boccio, Eric</name>
      </author>
    </item>
    <item>
      <title>A Case Report of Meningitis due to &lt;em&gt;Borrelia&lt;/em&gt; Species in Arizona</title>
      <link>https://escholarship.org/uc/item/1bp3m668</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Lyme disease is most prevalent in the Northeast and Midwest regions of the United States, as well as northern California; however, cases have been reported in nonendemic areas, including the Southwestern United States. Atypical presentations or underreporting can cause delay in diagnosis.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present the case of a 22-year-old previously healthy man, who presented to our emergency department in metropolitan Phoenix with five days of headache, fever, meningismus, and photophobia, and later developed focal neurologic deficits consistent with Lyme meningitis. Cerebrospinal fluid was notable for lymphocytic pleocytosis, and Western blot for Borrelia burgdorferi Immunoglobulin-M antibodies was positive, which led us to Lyme meningitis as the unifying diagnosis. He was treated with intravenous ceftriaxone and his symptoms resolved.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights the importance...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1bp3m668</guid>
      <pubDate>Sat, 26 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Austin, Scott</name>
      </author>
      <author>
        <name>Tarzia, Tamlyn</name>
      </author>
      <author>
        <name>Saunders, Griffith</name>
      </author>
    </item>
    <item>
      <title>Atypical Presentation of Extensive Stanford Type A Aortic Dissection Initially Misattributed to Aspiration Pneumonia: A Case Report</title>
      <link>https://escholarship.org/uc/item/7r27x687</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acute aortic dissection is a life-threatening emergency that may present with nonspecific symptoms, particularly in older adults, leading clinicians to anchor on more common diagnoses.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; An 85-year-old man presented with four days of cough, weakness, and constipation after a recent emergency department (ED) visit due to food impaction after he choked on a carrot. A chest radiograph obtained the day before admission showed left basal consolidation, prompting referral for suspected aspiration pneumonia. In the ED, he appeared comfortable with no complaints of chest pain. Physical examination noted mild tachycardia and wheezes bilaterally and treatment was initiated with antibiotics and bronchodilators. A low-voltage electrocardiogram led to immediate point-of-care echocardiography, which demonstrated a large circumferential pericardial effusion, a markedly dilated aortic root, and right ventricular collapse. Computed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7r27x687</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Goldgof, Margalit</name>
        <uri>https://orcid.org/0009-0005-1573-2057</uri>
      </author>
      <author>
        <name>Nama, Ahmad</name>
      </author>
      <author>
        <name>Mujahed, Waseem</name>
        <uri>https://orcid.org/0000-0002-7044-5625</uri>
      </author>
    </item>
    <item>
      <title>Exercise-Induced Diaphragmatic Rupture with Intrathoracic Gastric Herniation: A Case Report</title>
      <link>https://escholarship.org/uc/item/4vr403qv</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; While abdominal pain is a common complaint in the emergency department (ED), it is key to obtain a diligent history and maintain a broad differential diagnosis. The development of exercise-induced diaphragmatic hernia is rare but can result in a high risk of morbidity and mortality.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;This is a case of a 24-year-old man who presented to the ED with acute-onset epigastric abdominal pain that began while performing “burpee” (squat thrust) exercises. Computed tomography of the abdomen and pelvis revealed diaphragmatic rupture with gastric herniation into the left hemithorax. The patient underwent emergent surgical intervention to reduce the intra-abdominal contents and repair the diaphragmatic defect.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;There are no prior reports of diaphragmatic hernia due to burpee exercises in the emergency medicine literature. Consideration of exercise-induced diaphragmatic hernia is necessary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4vr403qv</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Berkovits, Adam S.</name>
      </author>
      <author>
        <name>Berkeley, Ross P.</name>
      </author>
      <author>
        <name>Daphne, Gregory P.</name>
      </author>
      <author>
        <name>Ellis, MacKenzie A.</name>
      </author>
      <author>
        <name>Lin, Jeffery</name>
      </author>
      <author>
        <name>Chen, Karen P.</name>
      </author>
    </item>
    <item>
      <title>Prehospital Ultrasound to Identify Endotracheal Tube Dislodgment in an Infant: A Case Report</title>
      <link>https://escholarship.org/uc/item/4tt6g8c8</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Point-of-care ultrasound (POCUS) is well established as a useful adjunct for airway management in both adult and pediatric patients, including confirmation of successful endotracheal intubation. While suprasternal ultrasound of the trachea is the most described method for confirming endotracheal tube (ETT) placement, a focused lung exam can be used to rapidly identify appropriate ventilation in otherwise apneic patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; This case involves a one-month-old male infant who experienced an out-of-hospital cardiac arrest secondary to suspected sudden infant death syndrome. During resuscitation, an accidental extubation occurred after an attempt at securing the ETT with a commercial pediatric tube holder. Loss of end-tidal carbon dioxide (ETCO2) waveform was recognized immediately; however, emergency medical services clinicians questioned the device’s accuracy due to earlier failures of the ETCO2 monitor and the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4tt6g8c8</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wright, Nicholas A.</name>
        <uri>https://orcid.org/0009-0004-4869-0327</uri>
      </author>
      <author>
        <name>Lucas, Ryan</name>
      </author>
      <author>
        <name>Bailey, Peyton</name>
      </author>
    </item>
    <item>
      <title>Locked-In Syndrome from Delayed Vertebral Artery Dissection After Strangulation: A Case Report</title>
      <link>https://escholarship.org/uc/item/3tp9v6t4</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Vertebral artery dissection is a rare but life-threatening complication of strangulation. &amp;nbsp;Symptoms are often nonspecific and may not manifest immediately, complicating diagnosis. If prior neck trauma is not elicited during assessment, clinicians may miss a mechanistic link to prompt vascular imaging, leaving patients at risk for irreversible outcomes, as illustrated in this case.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 24-year-old woman presented to a critical access emergency department (ED) with nonspecific neurological symptoms that had largely resolved upon arrival. Her only reported history was vague head and neck pain, which she attributed to stress after leaving an abusive relationship several weeks earlier. &amp;nbsp;Hours later, while still in the ED, the patient experienced abrupt neurological deterioration. She was transferred to a regional medical center, where magnetic resonance imaging eventually revealed vertebral artery dissection...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3tp9v6t4</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Snippen, Jennifer R.</name>
      </author>
      <author>
        <name>Huynh, Kien</name>
      </author>
    </item>
    <item>
      <title>Subacute Microperforation of Right Atrial Pacemaker Lead Presenting with Shock due to Cardiac Tamponade: A Case Report</title>
      <link>https://escholarship.org/uc/item/3cw2c4rb</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Delayed cardiac tamponade is a rare but life-threatening complication following permanent pacemaker placement and may present with non-specific symptoms.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 66-year-old woman on oral anticoagulation who presented with generalized weakness, nausea, and profound hypotension four days after dual-chamber pacemaker placement. Initial evaluation demonstrated atrial fibrillation with rapid ventricular response, a normal chest radiographic findings, prerenal azotemia, and no evidence of device malfunction on interrogation. Point-of-care ultrasound (POCUS) performed in the emergency department revealed a large pericardial effusion with right atrial and right ventricular collapse and a plethoric inferior vena cava, consistent with cardiac tamponade. Emergent pericardiocentesis yielded 400 mL of sanguinous pericardial fluid with rapid hemodynamic improvement. Subsequent imaging revealed a 2-mm...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3cw2c4rb</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Zirulnik, Alexander</name>
      </author>
      <author>
        <name>Bennett, Briton</name>
      </author>
      <author>
        <name>Almousa, Siham</name>
      </author>
    </item>
    <item>
      <title>Acute Dystonia Following Ifosfamide Infusion in a Young Woman with Breast Angiosarcoma: A Case Report</title>
      <link>https://escholarship.org/uc/item/2xp5q8rh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Ifosfamide is an alkylating chemotherapeutic agent commonly used in the treatment of sarcomas and other malignancies. Neurotoxicity is a recognized adverse effect, most often presenting as encephalopathy. Acute movement disorders such as dystonia are rare and may be underrecognized in the emergency department.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a 22-year-old woman receiving combination chemotherapy with doxorubicin, ifosfamide, and mesna for breast angiosarcoma who developed acute right-sided neck spasms and involuntary movements within five minutes of initiating ifosfamide infusion. Vital signs were as follows: temperature, 98.0 degrees Fahrenheit; heart rate, 97 beats per minute; respiratory rate, 18 breaths per minute; blood pressure, 130/88 millimeters of mercury; and oxygen saturation, 99% on room air. Examination revealed sustained contraction of the right sternocleidomastoid and trapezius muscles with involuntary head deviation....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xp5q8rh</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Miller, William S.</name>
      </author>
      <author>
        <name>Niblett, Alyssa B.</name>
      </author>
      <author>
        <name>Khoury, Charles A.</name>
      </author>
    </item>
    <item>
      <title>From Staple Removal to Startle—The Unexpected Discovery of a Scalp Pseudoaneurysm: A Case Report</title>
      <link>https://escholarship.org/uc/item/1394c2vm</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Point-of-care ultrasound (POCUS) allows emergency physicians to rapidly diagnose vascular abnormalities, including pseudoaneurysms. Although commonly identified following vascular catheterization, traumatic pseudoaneurysms of superficial scalp arteries are rare.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; An 85-year-old woman receiving anticoagulation presented to the emergency department (ED) for removal of a scalp staple placed during treatment of a previously bleeding scalp wound. Physical examination revealed a persistent scalp hematoma. Point-of-care ultrasound demonstrated a hypoechoic collection with Doppler flow consistent with a pseudoaneurysm. Computed tomography angiography confirmed the diagnosis. Ultrasound-guided compression attempted in the ED resulted only in transient thrombosis. The patient subsequently underwent elective percutaneous embolization.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Emergency physician–performed POCUS can rapidly identify...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1394c2vm</guid>
      <pubDate>Sun, 20 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Stankard, Brendon</name>
      </author>
      <author>
        <name>Forrester, John</name>
      </author>
      <author>
        <name>Jose, Stephanie</name>
      </author>
      <author>
        <name>Cohen, Allison</name>
      </author>
      <author>
        <name>Nelson, Mathew</name>
      </author>
    </item>
    <item>
      <title>Luxatio Erecta with Complex Medical Decision-Making Regarding Reduction: A Case Report</title>
      <link>https://escholarship.org/uc/item/884004wt</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Luxatio erecta is a rare glenohumeral dislocation. The standard treatment is reduction under procedural sedation; however, decision-making becomes more nuanced in patients with comorbidities. This report describes a hyperglycemic patient with type 1 diabetes with luxatio erecta.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; An 18-year-old man resented with a traumatic inferior shoulder dislocation. Laboratory tests indicated severe hyperglycemia without diabetic ketoacidosis. The emergency department team performed a risk-benefit assessment before proceeding with procedural sedation. Closed reduction was successful, and hyperglycemia was managed with intravenous fluids.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Inferior shoulder dislocations are rare; severe hyperglycemia in diabetics is not an absolute contraindication to procedural sedation, but the patient may need individualized risk-benefit assessment.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/884004wt</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Daniel, Mitch</name>
      </author>
      <author>
        <name>Deutsch, Aaron B.</name>
      </author>
      <author>
        <name>Greenberg, Marna R.</name>
      </author>
    </item>
    <item>
      <title>Gaze-Evoked Vomiting After Minor Orbital Trauma: White-Eyed Blowout Fracture</title>
      <link>https://escholarship.org/uc/item/81m7799m</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation:&lt;/strong&gt; A 16-year-old girl presented to the emergency department after being struck in the right eye by another player’s elbow during a basketball game. She had only minimal periorbital swelling but developed persistent nausea, repeated vomiting, and diplopia with upward gaze. Visual acuity, visual fields, and pupillary light reflexes were normal. Extraocular movement testing showed mild limitation of upward gaze of the right eye, and upward gaze reproducibly provoked diplopia, marked nausea, and vomiting. Computed tomography (CT) showed no intracranial hemorrhage, and orbital CT was initially interpreted as showing no obvious orbital floor fracture or extraocular muscle entrapment. Given the discrepancy between the mild external appearance and the severe ocular symptoms, white-eyed blowout fracture with trapdoor-type entrapment and an oculocardiac reflex was suspected. She underwent emergent surgery, after which her vomiting, diplopia, and ocular...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/81m7799m</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yamada, Naoki</name>
        <uri>https://orcid.org/0000-0001-8556-9009</uri>
      </author>
      <author>
        <name>Kato, Yukinori</name>
      </author>
    </item>
    <item>
      <title>Subarachnoid Pneumocephalus Following Endoscopic Transsphenoidal Surgery</title>
      <link>https://escholarship.org/uc/item/6vm7k9kd</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 26-year-old man with past medical history of prolactinoma presented two weeks status post endoscopic transsphenoid prolactinoma excision with a positional headache and cerebrospinal fluid rhinorrhea; he was found to have diffuse subarachnoid air.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion: &lt;/strong&gt;There are few reports of subarachnoid pneumocephalus in the emergency medicine literature. Pneumocephalus, particularly tension pneumocephalus, typically occurs in the setting of traumatic skull fractures. However, emergency physicians should be aware of subarachnoid pneumocephalus in the setting of endoscopic skull base surgeries.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6vm7k9kd</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dong, Willie</name>
      </author>
      <author>
        <name>Rothenberg, Roger</name>
      </author>
    </item>
    <item>
      <title>Medicolegal Pitfalls in Management of Shoulder Dislocations: A Case Series</title>
      <link>https://escholarship.org/uc/item/6sh2t32p</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Shoulder dislocations comprise approximately half of all major joint dislocations evaluated in the emergency department. Despite often being considered a simple injury, diagnosing a dislocation can be difficult, especially when accompanied by a fracture associated with unusual mechanism, or when the physical examination is limited. Missed and delayed diagnoses can result in poor patient outcomes and legal risks for clinicians, necessitating a high level of vigilance.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series: &lt;/strong&gt;We review three medical malpractice cases centered on the failure to recognize shoulder dislocations. Key issues included missed diagnosis, limited physical examination documentation, and inadequate discharge instructions.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Shoulder dislocations can be challenging to identify, and missed diagnoses give rise to subsequent clinical and legal risks. Emergency physicians must maintain a high index of suspicion...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6sh2t32p</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Billings, Clara</name>
      </author>
      <author>
        <name>Thomas, Aaron</name>
      </author>
      <author>
        <name>Bardwell, Abigail</name>
      </author>
      <author>
        <name>Lindor, Rachel</name>
        <uri>https://orcid.org/0000-0003-3099-8388</uri>
      </author>
    </item>
    <item>
      <title>Bezold Abscess: A Case Report</title>
      <link>https://escholarship.org/uc/item/57d6r7k9</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; A Bezold abscess is a neck abscess characterized by inflammation and infection of the mastoid process that can invade deep into local anatomical musculature and vasculature.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We highlight the case of a 62-year-old man who presented with ongoing left-sided neck pain, headache, and tinnitus that started two weeks prior to arriving at the emergency department. Physical examination showed tenderness to the left trapezius muscle, left-sided mastoid tenderness, and pearly tympanic membranes bilaterally. A computed tomography angiogram of the head and neck was performed due to concerns of vertebral dissection, which eventually led to a diagnosis of Bezold abscess.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Although Bezold abscess has been described in the medical literature, it is rarely encountered in modern clinical practice because the widespread use of antibiotic therapy prevents acute mastoiditis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/57d6r7k9</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wahhab, John</name>
      </author>
      <author>
        <name>Oganesyan, Ani</name>
      </author>
      <author>
        <name>Pham, Peter</name>
      </author>
      <author>
        <name>Jackson, Evan</name>
      </author>
    </item>
    <item>
      <title>The Stellate Ganglion Nerve Block—A Novel Use for Electrical Storm in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/2c63h6vn</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Electrical storm is an emergent medical condition in which a patient experiences recurrent episodes of ventricular tachycardia or ventricular fibrillation. Traditional management includes intravenous antiarrhythmics and/or electrical cardioversion. However, in some cases, cardiac arrhythmias may persist despite these interventions. In rare circumstances, traditional therapies in the emergency department (ED) may prove to be futile. In such cases, a stellate ganglion nerve block (SGNB) can be considered.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We present a novel case in which a SGNB was performed in the ED on an awake patient experiencing recurrent cardioversions from his implantable cardioverter defibrillator shocks for ventricular tachycardia.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; In the setting of refractory ventricular dysrhythmias, sympathetic blockade of the left stellate ganglion can be a useful adjunct to conventional management in the ED.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2c63h6vn</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Smith, Allison</name>
        <uri>https://orcid.org/0000-0002-1978-3370</uri>
      </author>
      <author>
        <name>Weindruch, Louisa</name>
      </author>
      <author>
        <name>Mayo, Rebecca</name>
      </author>
      <author>
        <name>Brewer, Jonathan</name>
        <uri>https://orcid.org/0000-0001-9300-3670</uri>
      </author>
    </item>
    <item>
      <title>Inferior Vena Cava Cement Migration with Pulmonary Cement Embolism: A Case Report</title>
      <link>https://escholarship.org/uc/item/1xj6c2dd</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Vertebral augmentation procedures, including vertebroplasty and kyphoplasty, can result in cement extravasation, which is often clinically silent. Less commonly, cement may migrate intravascularly into the inferior vena cava (IVC) and pulmonary arterial circulation, resulting in pulmonary cement embolism, a potentially life-threatening complication. Early recognition in the emergency department (ED) is essential to guide appropriate imaging, specialty consultation, and timely management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 76-year-old woman with recent third lumbar vertebral augmentation presented to the ED with acute worsening low back pain and burning bilateral radicular symptoms approximately one week after the procedure. Computed tomography (CT) of the abdomen and pelvis with intravenous contrast demonstrated linear hyperdense material extending from the treated vertebral body into the IVC, concerning for intravascular cement migration....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1xj6c2dd</guid>
      <pubDate>Tue, 8 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sneed, Christina Sneed</name>
      </author>
      <author>
        <name>Adnan, Syed</name>
      </author>
    </item>
    <item>
      <title>Observation Unit Management of Older Adults with Rib Fractures: A Case Series</title>
      <link>https://escholarship.org/uc/item/7vx7j3nh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Rib fractures in older adults carry high morbidity and mortality, leading many hospitals to admit patients based on age alone. The Rib Injury Guidelines (RIG) offer a triage system; under RIG 2, patients are typically admitted to inpatient care.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series: &lt;/strong&gt;This study evaluated whether older adults categorized as RIG 2 solely due to age could be safely managed in an emergency department observation unit. We conducted a 14-month case series at an academic trauma center, reviewing 23 patients 60 years and older with rib fractures. Twenty met RIG 2 criteria, including those later admitted for nontrauma reasons. The mean observation stay was 26.6 hours, and the total hospital stay was 1.8 days. Seventeen patients (85%) were discharged directly from observation, three (15%) were admitted to medicine, and none returned within 72 hours.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Carefully selected older adults with rib fractures...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vx7j3nh</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jenkins, Phillip D</name>
      </author>
      <author>
        <name>Crawford Rowe, Elizabeth K</name>
      </author>
      <author>
        <name>Gershon, Colin</name>
      </author>
      <author>
        <name>Cook, Mackenzie</name>
      </author>
      <author>
        <name>Marshall, John</name>
      </author>
    </item>
    <item>
      <title>Prehospital Cold-Water Immersion for Undifferentiated Heat Stroke: A Case Series</title>
      <link>https://escholarship.org/uc/item/72j8r9s4</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Heat stroke is a time-sensitive condition that requires early intervention to prevent morbidity and mortality. Heat-related deaths are also increasing. Multiple studies have evaluated various cooling methods and assessed their effectiveness, safety, and practicality across diverse settings and populations. Earlier and faster cooling leads to improved patient outcomes. The National Association of Emergency Medical Services Physicians recommends initiating prehospital cold-water immersion before emergency medical services (EMS) transport.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series: &lt;/strong&gt;This case series evaluated the feasibility and effectiveness of prehospital cold-water immersion initiated before and continued during EMS transportation from the scene to emergency department arrival in this critically ill patient population.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Rapid initiation and maintenance of prehospital cold-water immersion in undifferentiated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/72j8r9s4</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lindow, David</name>
      </author>
      <author>
        <name>Everitt, Bryan</name>
      </author>
      <author>
        <name>Smith, Nick</name>
      </author>
      <author>
        <name>Wells, Michael</name>
      </author>
      <author>
        <name>Dickson, Robert</name>
      </author>
      <author>
        <name>Patrick, Casey</name>
      </author>
    </item>
    <item>
      <title>Tension Pneumopericardium from a Gastrojejunal-Pericardial Fistula Causing Tamponade: A Case Report</title>
      <link>https://escholarship.org/uc/item/72g5m4qp</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Cardiac tamponade typically develops from the accumulation of blood and other fluids, although it can occur from pneumopericardium.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 62-year-old man presented to the emergency department with chest pain and was found to have a pneumopericardium on computed tomography. He developed signs of obstructive shock with hypotension refractory to intravenous fluids and vasopressors. The patient stabilized with bedside pericardiocentesis and pericardial drain placement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Gastrointestinal-pericardial fistulae are a rare cause of pneumopericardium. Emergency physicians typically rely on cardiac point-of-care ultrasound to evaluate for tamponade and guide pericardiocentesis. However, air artifacts interfere with images, complicating diagnosis and procedures.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/72g5m4qp</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Moscinski, Catherine</name>
      </author>
      <author>
        <name>Altheimer, Alyssa</name>
      </author>
      <author>
        <name>Driver, Lachlan</name>
      </author>
      <author>
        <name>Maryanov, Nikita</name>
      </author>
      <author>
        <name>Cunningham, Cassidy</name>
        <uri>https://orcid.org/0000-0002-7357-7092</uri>
      </author>
    </item>
    <item>
      <title>Unna Boot Therapy Reduces Emergency Department Use in an&amp;nbsp;Unhoused Patient: A Case Report</title>
      <link>https://escholarship.org/uc/item/594347pw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Venous leg ulcers disproportionately affect people experiencing homelessness and contribute to recurrent emergency department (ED) use. Standard wound care protocols often require daily dressing changes and leg elevation, which are unrealistic in unstable housing environments.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 71-year-old male with a 10-year history of venous leg ulcers and 15 ED visits achieved complete wound epithelialization after four months of weekly Unna boot compression therapy, despite eviction during treatment. He has not returned to the ED for this condition.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Emergency department-initiated compression therapy with structured wound care referral may reduce recurrent ED use among unhoused patients with venous leg ulcers.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/594347pw</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Coba Clementel, Ariana</name>
        <uri>https://orcid.org/0009-0001-4708-4649</uri>
      </author>
      <author>
        <name>Ross, Frank</name>
      </author>
    </item>
    <item>
      <title>Amphetamine-induced Reverse Takotsubo Syndrome: Further Implications</title>
      <link>https://escholarship.org/uc/item/57x0j0hk</link>
      <description>&lt;p&gt;Amphetamine-induced Reverse Takotsubo Syndrome: Further Implications&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/57x0j0hk</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yalta, Kenan</name>
      </author>
      <author>
        <name>Gok, Murat</name>
      </author>
    </item>
    <item>
      <title>Soft Palate Perforation with Endotracheal Tube During Video Laryngoscopy</title>
      <link>https://escholarship.org/uc/item/41m7s14z</link>
      <description>&lt;p&gt;&lt;strong&gt;Case presentation:&lt;/strong&gt; A 57-year-old man with a history of obesity-hypoventilation syndrome, diabetes mellitus, and chronic renal insufficiency was intubated with an 8.0-mm endotracheal tube under video laryngoscopy in the emergency department due to respiratory failure. After successful intubation, bloody secretions were noted in the patient’s mouth. Subsequent examination revealed that the endotracheal tube had caused a through-and-through perforation at the junction of the soft palate and the anterior tonsillar pillar. Because the intubation had been successful, the endotracheal tube was not removed, and the soft palate was transected to free the tube. The patient made an uneventful recovery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion:&lt;/strong&gt; Soft palate perforation is an uncommon injury that has been reported more frequently with video laryngoscopy than direct laryngoscopy. To prevent this injury and ensure its rapid recognition, it is recommended that the clinician sequentially...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/41m7s14z</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Thomas, Samuel J.</name>
        <uri>https://orcid.org/0009-0004-1644-7074</uri>
      </author>
      <author>
        <name>Zimmer, David I.</name>
        <uri>https://orcid.org/0000-0001-8656-2175</uri>
      </author>
      <author>
        <name>Langford, Jack H.</name>
      </author>
      <author>
        <name>Brenner, Toby J.</name>
        <uri>https://orcid.org/0000-0002-5970-9730</uri>
      </author>
      <author>
        <name>Kelly, Kate M.</name>
      </author>
      <author>
        <name>Zimmer, Donald F.</name>
      </author>
    </item>
    <item>
      <title>Primary Group A Streptococcus Peritonitis&amp;nbsp;in a Healthy Child: A Case Report</title>
      <link>https://escholarship.org/uc/item/2bn8g84j</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Group A streptococcus (GAS, Streptococcus pyogenes) is commonly associated with pharyngitis and skin and soft tissue infections, but invasive infection can occur. Primary bacterial peritonitis due to GAS is rare, especially in healthy children without nephrotic syndrome or immunocompromise.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present a 21-month-old previously healthy male with four days of fever, irritability, and refusal to walk. Examination revealed abdominal distention and peritonitis. Computed tomography showed ascites and a normal appendix. Diagnostic laparoscopy revealed copious purulent peritoneal fluid; both peritoneal fluid and blood cultures were positive for GAS. He was treated with ampicillin-sulbactam followed by oral amoxicillin-clavulanate with complete recovery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;This case highlights a rare presentation of invasive GAS as primary peritonitis in a healthy child. Clinicians should consider this...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2bn8g84j</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Drinnan, Alex</name>
      </author>
      <author>
        <name>Naprawa, James</name>
      </author>
      <author>
        <name>Kim, Sunghoon</name>
      </author>
      <author>
        <name>Mansour, Karim</name>
      </author>
    </item>
    <item>
      <title>A Case Report of Spontaneous Pneumomediastinum Following Chest Massage: A Rare Clinical Presentation</title>
      <link>https://escholarship.org/uc/item/0gd6z5hd</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&amp;nbsp;&lt;/strong&gt;Spontaneous pneumomediastinum is a rare condition characterized by the presence of air in the mediastinum without preceding trauma. It is often triggered by minor events such as coughing, physical exertion, or traditional therapies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 52-year-old male with a history of pulmonary tuberculosis developed sudden left-sided chest pain and swelling following traditional chest massage therapy. Examination revealed subcutaneous emphysema with palpable crepitus. Imaging showed characteristic signs of pneumomediastinum with bilateral lung opacities. As a complication of pneumomediastinum the patient developed mediastinitis and a mediastinal abscess, requiring open thoracotomy and drainage. He recovered with multidisciplinary care.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Early recognition of spontaneous pneumomediastinum in emergency settings is crucial, especially when chest pain is accompanied by subcutaneous...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0gd6z5hd</guid>
      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>H, Naveed Ul Hassan</name>
        <uri>https://orcid.org/0009-0002-3920-0758</uri>
      </author>
      <author>
        <name>B G, Kowsthubha</name>
        <uri>https://orcid.org/0009-0006-7909-7248</uri>
      </author>
      <author>
        <name>Uthayakumar, Amaravathi</name>
      </author>
    </item>
    <item>
      <title>Purulent Pericarditis Identified with Point-of-Care Echocardiography: A Case Report</title>
      <link>https://escholarship.org/uc/item/5jw302zf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Purulent pericarditis is a rare subset of pericarditis that can result in serious morbidity and mortality. Presenting symptoms are often nonspecific, and a high index of suspicion must be maintained to reach an early diagnosis. Point-of-care ultrasound can be pivotal in the emergency department evaluation of purulent pericarditis, providing key information including characteristics of the effusion and a sonographic assessment for signs of tamponade. We present a case of purulent pericarditis first detected using point-of-care ultrasound in the emergency department.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 55-year-old male presented with chest pain and dyspnea and was found to have cardiac tamponade secondary to purulent pericarditis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Cases of purulent pericarditis are rare but should be recognized by emergency clinicians. Point-of-care ultrasound is a powerful tool to assist in early diagnosis of pericardial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jw302zf</guid>
      <pubDate>Mon, 24 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Baquet, Daniel</name>
      </author>
      <author>
        <name>Blevins, Aaron</name>
      </author>
      <author>
        <name>Casey, Dillon</name>
      </author>
      <author>
        <name>Glass, Casey</name>
      </author>
      <author>
        <name>Seaback, Jordan</name>
      </author>
      <author>
        <name>Schoeneck, Jacob</name>
      </author>
    </item>
    <item>
      <title>Retrograde Intubation in a Severe Fixed Spinal Deformity: A Case Report</title>
      <link>https://escholarship.org/uc/item/9fq820rz</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Retrograde intubation is a seldom used but valuable technique in managing difficult airways, especially in resource‑limited settings when advanced equipment is unavailable or ineffective.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 64‑year‑old male with advanced ankylosing spondylitis and severe cervicothoracolumbar kyphosis who presented with altered mental status and respiratory distress. Extreme fixed cervical flexion, markedly restricted mouth opening, and an inaccessible anterior neck rendered direct laryngoscopy, video laryngoscopy, fiberoptic intubation, and surgical airway approaches unfeasible. Retrograde nasotracheal intubation was successfully performed, resulting in airway stabilization and hemodynamic improvement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights retrograde intubation as a lifesaving low‑technology technique in complex anatomic and physiologic airways, demonstrating its continued relevance...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9fq820rz</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Joshi, Shrirang Shriram</name>
        <uri>https://orcid.org/0000-0002-0913-852X</uri>
      </author>
      <author>
        <name>Nayak, Shreesha</name>
      </author>
      <author>
        <name>Chakraborty, Shoubhik</name>
      </author>
      <author>
        <name>Kaur, Hardeep</name>
      </author>
      <author>
        <name>Siddiqua, Naazia</name>
      </author>
      <author>
        <name>Bhoi, Sanjeev</name>
      </author>
    </item>
    <item>
      <title>It’s A Pain in The Neck: Case Report of Bedside Diagnosis of&amp;nbsp;Unilateral Neck Swelling</title>
      <link>https://escholarship.org/uc/item/99b4z9x7</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Lemierre syndrome is a rare but potentially severe thrombophlebitis of the internal jugular vein. It most often presents after oropharyngeal infection, likely stemming from anaerobic&amp;nbsp;bacteria, commonly&amp;nbsp;&lt;em&gt;Fusobacterium necrophorum&lt;/em&gt;. The potential severity of this condition&amp;nbsp;underscores the importance of early and accurate diagnosis. The gold standard diagnosis relies on&amp;nbsp;computed tomography and blood cultures; however, point-of-care ultrasound offers a rapid and cost-effective tool.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A 58-year-old woman with chronic obstructive pulmonary disease, migraines, and&amp;nbsp;recent dental extractions presented with two days of worsening right-sided neck pain and swelling.&amp;nbsp;She denied fever, chills, or recent upper respiratory symptoms. Examination revealed a tender&amp;nbsp;anterior neck mass without airway compromise. Point-of-care ultrasound demonstrated a 1.22 x&amp;nbsp;1.80 centimeters hyperechoic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/99b4z9x7</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Hotton, Maxx F</name>
      </author>
      <author>
        <name>Roth, Kevin R</name>
      </author>
      <author>
        <name>Schultz, Kristine L</name>
      </author>
    </item>
    <item>
      <title>Unusual Etiology and Presentation for Hyperkalemia - Dialysis Access Recirculation: A Case Report</title>
      <link>https://escholarship.org/uc/item/92c6n3wt</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Hyperkalemia is a common and potentially life-threatening complication of end-&amp;nbsp;stage renal disease, often producing nonspecific symptoms but profound cardiac effects. While&amp;nbsp;nonadherence and dietary indiscretion are typical precipitants, clinicians must also consider the adequacy and effectiveness of dialysis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;:&amp;nbsp;We report a patient with end-stage renal disease on thrice-weekly hemodialysis who&amp;nbsp;presented with significant bradycardia and altered mental status. Initial prehospital electrocardiogram&amp;nbsp;(ECG) was suspicious for acute coronary syndrome after automated ECG interpretation suggested&amp;nbsp;anterior ST-segment elevation. In the emergency department, the patient was in a junctional&amp;nbsp;escape rhythm with diffuse peaked T-waves. Serum potassium was 7.8 millimoles per liter with&amp;nbsp;concomitant uremia. Despite administration of potassium-shifting therapies bradycardia persisted,&amp;nbsp;and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/92c6n3wt</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Joseph Lim</name>
        <uri>https://orcid.org/0009-0000-4922-8514</uri>
      </author>
      <author>
        <name>Glazer, Joshua</name>
      </author>
      <author>
        <name>Achufusi, Amaka E.</name>
        <uri>https://orcid.org/0000-0002-4628-2993</uri>
      </author>
      <author>
        <name>Tsuchida, Ryan Ellis</name>
      </author>
    </item>
    <item>
      <title>Use of Corrected QT Cutoffs Derived from Biological Variation to Predict Adverse Events Due to Antipsychotic Drugs: Case Report</title>
      <link>https://escholarship.org/uc/item/8j7267dj</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The use of antipsychotic drugs can prolong the corrected QT (QTc) interval of the electrocardiogram and cause a life-threatening ventricular arrhythmia. There is no consensus as to what is considered normal or what cutoff indicates QTc prolongation. However, recent literature has described the biological variation of the QTc interval from healthy subjects, with researchers concluding that the best approach at establishing a normal range is to determine an individual baseline interval during health.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A baseline QTc interval (460 milliseconds) had been determined for a 42-year-old female with a history of schizophrenia and depression who was prescribed antipsychotic drugs including escitalopram, olanzapine, haloperidol, clonazepam and divalproex over the course of four years. Over that time frame, she was admitted on 20 occasions with chest pain, but her QTc interval was at or above her baseline level. Acute...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8j7267dj</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Alan H.B.</name>
      </author>
      <author>
        <name>Alamillo, Melissa</name>
      </author>
      <author>
        <name>Kendrick, Kayla</name>
      </author>
    </item>
    <item>
      <title>Clinical Practice and Cases in Emergency Medicine Volume 10 Issue 3</title>
      <link>https://escholarship.org/uc/item/8bg1w4xd</link>
      <description>Clinical Practice and Cases in Emergency Medicine Volume 10 Issue 3</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8bg1w4xd</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>CPC-EM, Clinical Practice and Cases in Emergency Medicine</name>
      </author>
      <author>
        <name>Saucedo, Cassandra</name>
      </author>
      <author>
        <name>Haghkhah, Omid</name>
      </author>
    </item>
    <item>
      <title>Incidental Wolff-Parkinson-White Syndrome Discovered&amp;nbsp;Following Dicyclomine Use: A Case Report</title>
      <link>https://escholarship.org/uc/item/74x388s6</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Wolff-Parkinson-White syndrome is a congenital conduction disorder involving an accessory pathway that predisposes patients to reentrant tachyarrhythmias and, in rare cases, sudden cardiac death. While often asymptomatic, it may predispose patients to serious tachyarrhythmias, particularly under conditions that enhance atrioventricular (AV) conduction. Risk stratification using noninvasive and invasive tools such as electrophysiologic studies is critical&amp;nbsp;to identifying high-risk individuals and guiding treatment decisions such as catheter ablation.&amp;nbsp;Pharmacologic agents that alter autonomic tone may unmask latent pre-excitation. Dicyclomine, an&amp;nbsp;anticholinergic agent used for gastrointestinal disorders, is not an&amp;nbsp;AV-nodal blocking drug but exerts&amp;nbsp;vagolytic effects that can increase sinus rate and AV nodal conduction. Dicyclomine’s vagolytic&amp;nbsp;effects and potential for interaction with other proarrhythmic drugs warrant...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/74x388s6</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wahhab, John</name>
      </author>
      <author>
        <name>Loveridge, Natalie Margaret</name>
      </author>
      <author>
        <name>Siaj, Manar</name>
      </author>
    </item>
    <item>
      <title>Popliteal Artery Aneurysm Thrombosis Diagnosed with&amp;nbsp;Point-of-Care Ultrasound</title>
      <link>https://escholarship.org/uc/item/6x79r7pf</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 62-year-old male presented to the emergency department with a three-day history of right knee, calf, and foot pain following a bout of prolonged crouching while gardening. The physical examination revealed a cold and pale foot with absent pulses. A point-of-care ultrasound (POCUS) performed at bedside revealed a thrombosed popliteal artery aneurysm. A heparin infusion was initiated, and vascular surgery was consulted. Subsequent imaging confirmed the diagnosis of a thrombosed popliteal artery aneurysm with thrombus extension into the superficial femoral artery. The patient underwent a femoropopliteal bypass, resulting in successful revascularization of the limb.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion: &lt;/strong&gt;While POCUS is a well-established imaging modality for the diagnosis of deep vein thrombosis, its utility in diagnosing acute peripheral arterial pathologies is less well-known. This case demonstrates how prompt bedside POCUS evaluation can circumvent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6x79r7pf</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gonedes, Andrew</name>
      </author>
      <author>
        <name>Kohen, Brian</name>
      </author>
      <author>
        <name>Diallo, Alfa</name>
      </author>
      <author>
        <name>McKenna, Mark</name>
      </author>
      <author>
        <name>Farrow II, Robert</name>
      </author>
      <author>
        <name>Boccio, Eric</name>
      </author>
    </item>
    <item>
      <title>Fishing Hook Globe Injury Diagnosed with Point-of- care Ultrasound: A Case Report</title>
      <link>https://escholarship.org/uc/item/6rz50010</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Globe injuries constitute true ophthalmologic emergencies and require prompt surgical intervention. When direct physical examination is limited, due to trauma or swelling, point-of-care ultrasound (POCUS) can serve as a valuable adjunct in evaluating globe integrity.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 31-year-old male who presented to the emergency department with a barbed fishing hook embedded in his right eyelid. The patient reported pain localized to the eyelid but denied any visual disturbances or direct eye involvement. On examination, a large fishing hook embedded in the right upper eyelid was visualized. His eye was swollen, and he was unable to fully open it, limiting direct assessment of the globe. Given the limited exam, POCUS of the right eye revealed a foreign body traversing the anterior chamber toward the lens, raising concern for globe injury. Ophthalmology was consulted, and computed tomography of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6rz50010</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Carter, Jeremy</name>
      </author>
      <author>
        <name>Zatarain, John Robert</name>
      </author>
      <author>
        <name>Zatarain, Mia</name>
      </author>
      <author>
        <name>Koscumb, Paul</name>
      </author>
      <author>
        <name>Paul, Krishna</name>
      </author>
      <author>
        <name>Jehle, Dietrich</name>
        <uri>https://orcid.org/0009-0002-6006-3903</uri>
      </author>
    </item>
    <item>
      <title>Use of Balloon Tamponade Device for Aortoesophageal Fistula: A Case Report</title>
      <link>https://escholarship.org/uc/item/6rh5n8kv</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Aortoesophageal fistula is a rare but life-threatening hemorrhagic complication of thoracic endovascular aortic repair. Without intervention, mortality approaches 100%. Our case highlights the utility of using an esophageal-gastric balloon tamponade device for hemostasis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 70-year-old man who presented after a sentinel episode of hematemesis six days after thoracic endovascular aortic repair. Shortly after admission, the patient developed massive hematemesis and hemorrhagic shock from an aortoesophageal fistula. Hemorrhage was temporarily controlled via bedside placement of a Minnesota tube, a type of balloon tamponade device, by two emergency medicine and critical care physicians, allowing for hemostasis, resuscitation, and definitive diagnosis with esophagogastroduodenoscopy. The device successfully bridged the patient to the operating room, where he underwent definitive endovascular...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6rh5n8kv</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Burton, Erich</name>
        <uri>https://orcid.org/0009-0000-9299-4767</uri>
      </author>
      <author>
        <name>Wray, Trenton</name>
      </author>
    </item>
    <item>
      <title>Clinical Application of Intravenous Lipid Emulsion Therapy in&amp;nbsp;Cocaine-associated Cardiac Arrest: A Case Report</title>
      <link>https://escholarship.org/uc/item/6dc9d00z</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Cardiac arrest in the setting of cocaine use portends high morbidity and mortality&amp;nbsp;secondary to its powerful sodium channel blockade effects. Intravenous (IV) lipid emulsion has long&amp;nbsp;been used as a rescue therapy in lipophilic toxicities.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We report a case in which IV lipid emulsion was used to successfully stabilize a&amp;nbsp;patient who suffered cocaine-associated, out-of-hospital cardiac arrest.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;Intravenous lipid emulsion was used in the successful resuscitation of a cocaine&amp;nbsp;overdose and could be considered for use in patients with cocaine-associated cardiac arrest.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6dc9d00z</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Offman, Ryan</name>
      </author>
      <author>
        <name>Baribeau, Sarah K</name>
      </author>
    </item>
    <item>
      <title>Elderly Male with a Painful Red Eye</title>
      <link>https://escholarship.org/uc/item/68g1v3hg</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;An 83-year-old man with a history of left corneal transplant presented to the emergency department with several days of left eye pain, redness, and tearing. Visual acuity was 20/50 in the right eye and bare light perception in the left eye. Intraocular pressure was 15 millimeters fo mercury in the right eye and unobtainable in the left. The left conjunctiva and sclera were injected, and slit-lamp examination revealed a full-thickness corneal perforation with corneal haze in the transplanted cornea. We placed a rigid eye shield, provided systemic analgesia, kept the patient nil per os, and obtained urgent ophthalmology consultation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion:&lt;/strong&gt; Corneal perforation is a full-thickness corneal defect that disrupts globe integrity and allows aqueous leakage. It may result from infection, ocular surface disease, autoimmune disorders, trauma, or prior keratoplasty, with graft–host junction instability representing a key...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/68g1v3hg</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dahdal, Diala</name>
      </author>
      <author>
        <name>Nama, Ahmad</name>
      </author>
      <author>
        <name>Deng, Wenyu</name>
      </author>
      <author>
        <name>Hahn, Barry</name>
        <uri>https://orcid.org/0000-0001-9035-5603</uri>
      </author>
    </item>
    <item>
      <title>Subungual Myiasis Presenting to the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/67t9g0sh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Subungual myiasis is an infection under the fingernail or toenail caused by an infestation of fly larvae. It is rarely reported internationally, with only one previously reported case in the United States.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;An 80-year-old female with a history of polyneuropathy, peripheral artery disease, peripheral venous insufficiency, and chronic bilateral lower extremity edema presented to the emergency department (ED) after staff at her skilled nursing facility noted what appeared to be several whitish-colored maggots moving under the nail of the patient’s left great toe. Thorough examination was consistent with subungual myiasis with associated onycholysis without evidence of associated cellulitis or soft tissue infection. Manual extraction of six larvae was performed, and the patient’s foot was soaked in chlorhexidine. She was discharged back to her facility with a plan for daily chlorhexidine soaks and prompt follow-up...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/67t9g0sh</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Marquis, Taylor</name>
      </author>
      <author>
        <name>Sheng, Alexander Y</name>
      </author>
    </item>
    <item>
      <title>Tension Hydrocele—How Point-of-care Ultrasound Helps in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/67n326s9</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Tension hydrocele is a rare but serious complication that can threaten testicular viability. This case report describes how testicular point-of-care ultrasound (POCUS) enabled timely recognition of a large hydrocele compromising testicular perfusion and guided management.&lt;br&gt;Case Report: A 57-year-old male presented to the emergency department (ED) with painful right scrotal swelling. Testicular POCUS demonstrated a large hydrocele with reduced intratesticular blood flow. A scrotal centesis performed by the emergency physician led to symptom resolution and restoration of normal flow.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Testicular POCUS can rapidly identify impaired perfusion and guide scrotal centesis in the ED, a temporary yet potentially testis-saving intervention.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/67n326s9</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Potalivo, Sophia</name>
      </author>
      <author>
        <name>Fornbacher, Sophia</name>
      </author>
      <author>
        <name>Abadilla, Joey</name>
      </author>
      <author>
        <name>Goubert, Ron</name>
      </author>
      <author>
        <name>Tovar Hirashima, Eva</name>
      </author>
    </item>
    <item>
      <title>Yellow Granular Material in Hair: A Bedside Clue to Overdose from Cold Medication Containing Acetaminophen</title>
      <link>https://escholarship.org/uc/item/6785283v</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 28-year-old woman was brought to the emergency department after being found collapsed at home. Because she was unable to provide a history, contextual bedside clues were important during the initial assessment. Bright yellow granular material with a medicinal odor was noted adherent to her hair. This unusual finding raised suspicion of overdose with an acetaminophen-containing over-the-counter (OTC) cold medication. Her serum acetaminophen concentration was elevated at 135 micrograms per milliliter, and N-acetylcysteine was promptly administered. She did not develop hepatic injury and was discharged after recovery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;D&lt;/strong&gt;&lt;strong&gt;iscussion:&lt;/strong&gt; This case highlights the diagnostic value of visible bedside clues when history is initially unavailable. The yellow residue was not pathognomonic, and no chemical analysis of the material was performed. However, in the context of the increasing incidence of overdoses involving...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6785283v</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sakamoto, So</name>
        <uri>https://orcid.org/0000-0002-0921-7375</uri>
      </author>
    </item>
    <item>
      <title>Adult Intussusception and Ischemic Bowel Potentially Associated with CurQD Supplementation: A Case Report of A Diagnosis Driven by Point-of-care Ultrasound</title>
      <link>https://escholarship.org/uc/item/5xk417k4</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Adult ileocolic intussusception is rare and typically associated with a pathological lead point. Diagnosis can be challenging in the emergency department (ED), particularly when initial vital signs and laboratory studies are reassuring. Point-of-care ultrasound (POCUS) may allow for earlier recognition and expedited management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A woman with ulcerative colitis presented to the ED with abrupt, severe, waxing-and-waning abdominal pain. Initial vital signs and lab studies were normal. Bedside POCUS performed at the point of maximal tenderness revealed a target sign in the right mid-abdomen, prompting concern for intussusception. This finding was used to advocate for urgent surgical evaluation and expedited computed tomography of the abdomen and pelvis, which confirmed ileocolic intussusception with early distal small-bowel obstruction and no identifiable mass. Despite reassuring objective data, the patient’s persistent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xk417k4</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Parambath, Andrew</name>
      </author>
      <author>
        <name>Patel, Bobby</name>
      </author>
      <author>
        <name>Batchelor, Timothy J.</name>
      </author>
      <author>
        <name>Ashenburg, Nicholas Geoffrey</name>
      </author>
      <author>
        <name>Ahern, Terence Lee</name>
      </author>
    </item>
    <item>
      <title>Dynamic Supraglottic Airway Collapse Diagnosed Using Airway Point-of-care Ultrasound: A Case Report</title>
      <link>https://escholarship.org/uc/item/5xj64561</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acquired idiopathic laryngomalacia causing dynamic airway collapse is rare in adolescents and may be overlooked because it mimics more common causes of acute dyspnoea and stridor in the emergency department (ED). Airway point-of-care ultrasound (POCUS) provides a rapid, non-invasive means to visualize dynamic supraglottic obstruction when laryngoscopy is not immediately feasible or tolerated.​&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A 13-year-old boy presented with sudden-onset respiratory distress and dyspnoea that worsened on lying flat and improved when sitting upright, without history of fever, trauma, allergy, or foreign body aspiration, and with similar prior self-limiting episodes. He was anxious with nasal flaring, subcostal retractions, tachypnoea, tachycardia, distended neck veins, and a squeaky tracheal inspiratory sound, yet he maintained normal oxygen saturation with equal air entry on auscultation. Airway POCUS showed abnormal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xj64561</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jain, Arihant</name>
        <uri>https://orcid.org/0000-0003-3729-8608</uri>
      </author>
      <author>
        <name>Mohammed Muthanikkatt, Anas</name>
        <uri>https://orcid.org/0000-0003-2325-4719</uri>
      </author>
      <author>
        <name>Ayyan, S. Manu</name>
      </author>
    </item>
    <item>
      <title>VenoArterial Extracorporeal Membrane Oxygenation in Cardiac Arrest Suspected due to Massive Pulmonary Embolism: A Case Report</title>
      <link>https://escholarship.org/uc/item/5rw263cs</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;High-risk pulmonary embolism (PE) is an uncommon but potentially reversible cause of out-of-hospital cardiac arrest, frequently presenting as pulseless electrical activity (PEA). Early identification and multidisciplinary intervention are critical, yet confirmatory imaging is often delayed. Current guidelines recommend consideration of venoarterial extracorporeal membrane oxygenation (VA-ECMO) support in specialized centers when high-risk PE is suspected and the patient presents with cardiogenic shock or cardiac arrest.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We describe a 50-year-old woman with a remote history of deep vein thrombosis who arrested after acute-onset dyspnea. Emergency medical services documented PEA arrest and initiated advanced cardiac life support. On arrival to the emergency department (ED), the patient remained in PEA arrest without cardiac motion on point-of-care ultrasound. Pulmonary embolism was strongly suspected but...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5rw263cs</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chopra, Tananshi</name>
      </author>
      <author>
        <name>Dahlke, Lea</name>
      </author>
      <author>
        <name>Salinas, Nancy</name>
      </author>
      <author>
        <name>Shabbir, Moizza</name>
      </author>
      <author>
        <name>Gunn, Tyler</name>
      </author>
      <author>
        <name>Torbati, Sam</name>
      </author>
    </item>
    <item>
      <title>Case Report: Lidocaine Toxicity Presenting with Focal Neurologic Findings</title>
      <link>https://escholarship.org/uc/item/5jf8p2sx</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Lidocaine toxicity is a rare but potentially dangerous consequence of a frequently used medication. Most commonly, it has generalized neurologic and cardiac effects. Discontinuation of lidocaine is sufficient with less severe symptoms. With more severe symptoms, such as seizures and arrhythmia, intravenous (IV) lipid emulsion therapy can be used. To date, lidocaine toxicity presenting as focal neurologic deficits has rarely been documented in the literature. In the case reported here, the patient was receiving lidocaine injections when she developed palpitations and left arm and facial weakness and numbness, which resolved after IV lipid emulsion therapy.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 52-year-old female with a past medical history of migraines, cholecystectomy, nephrolithiasis, and hypothyroidism presented to the emergency department (ED) via ambulance from her dental office with acute neurologic symptoms. While receiving an injection...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jf8p2sx</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yeung, Timothy</name>
      </author>
      <author>
        <name>Estrada, Isaac</name>
      </author>
      <author>
        <name>Phan, Tammy H.</name>
      </author>
      <author>
        <name>Samones, Emmelyn J.</name>
      </author>
      <author>
        <name>Kalam, Sharmin</name>
      </author>
    </item>
    <item>
      <title>Stretching the Limits: A Rare Case Report of Perimesencephalic Subarachnoid Hemorrhage During Yoga</title>
      <link>https://escholarship.org/uc/item/5g5672bk</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Nontraumatic subarachnoid hemorrhage (SAH) is a life-threatening neurological emergency, accounting for 5-10% of strokes. While most cases result from aneurysm rupture, perimesencephalic nonaneurysmal SAH is a distinct subtype characterized by blood localized to the midbrain cisterns and a venous pathophysiology. Perimesencephalic nonaneurysmal SAH is often associated with activities increasing intracranial venous pressure. Reports linking it to low-impact exercise such as yoga are rare.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 45-year-old female with no significant medical history presented with acute onset of severe headache and subjective unilateral hearing loss. Symptoms began immediately after a sudden, startled hyperextension movement during a yoga session. Noncontrast computed tomography of the brain revealed hemorrhage localized to the perimesencephalic and basal cisterns (modified Fisher Grade 4). Magnetic resonance imaging confirmed hemorrhage...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5g5672bk</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Vierra, Andrew</name>
      </author>
      <author>
        <name>Sinha, Mrinal</name>
      </author>
      <author>
        <name>Jamal, Leena</name>
      </author>
      <author>
        <name>Khan, Nadir</name>
      </author>
      <author>
        <name>Liebert, Taylor</name>
      </author>
      <author>
        <name>Bokhari, Abdullah</name>
      </author>
    </item>
    <item>
      <title>Differentiating Weakness—an Atypical Presentation of Acute Neuromuscular Paralysis: A Case Report</title>
      <link>https://escholarship.org/uc/item/5cf0r1x8</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Spinal cord infarction is a rare but critical cause of acute neuromuscular paralysis, accounting for approximately 1.2% of all strokes. Timely diagnosis is essential but challenging due to its clinical overlap with more common etiologies. Failure to promptly identify spinal cord infarction can result in irreversible neurological deficits and missed opportunities for secondary prevention.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 66-year-old female presented to the emergency department with progressive bilateral limb weakness, numbness, and urinary incontinence. The examination revealed symmetric weakness, impaired coordination, and diffuse sensory loss. She was admitted and empirically treated with intravenous immunoglobulin for suspected atypical acute inflammatory demyelinating polyneuropathy. Despite mild improvement, worsening hyperreflexia and spasticity raised concern for a central process. Cervical magnetic resonance imaging revealed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5cf0r1x8</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Golder, Jack</name>
      </author>
      <author>
        <name>Tjiattas-Saleski, Lindsay</name>
      </author>
    </item>
    <item>
      <title>Magnetic Mishaps—Small Bowel Obstruction Caused by Ingested Magnets Complicated by Appendicitis: A Case Report</title>
      <link>https://escholarship.org/uc/item/5383h1hh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Magnet ingestions are a growing pediatric emergency due to the use of widely available stronger magnets in toys. A legislative ban briefly reduced injuries, but cases rose after its reversal in federal court. Magnet ingestions are resulting in increasing morbidity and mortality, specifically due to bowel obstruction and perforation.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present a complex case involving a child with global developmental delay presenting to the emergency department for evaluation of abdominal pain. While the initial evaluation focused on working up appendicitis, which he was found to have, he was also found to have ingested multiple magnets causing small bowel obstruction and perforation.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&amp;nbsp;&lt;/strong&gt;This case highlights the need for emergency physicians to maintain a high level of suspicion when evaluating pediatric patients with abdominal pain, especially those with developmental delay....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5383h1hh</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ball, Seth</name>
      </author>
      <author>
        <name>Wierzbicki, Marissa</name>
      </author>
    </item>
    <item>
      <title>Seven-year-old Girl with Vomiting, Diarrhea, and Decreased Oral Intake</title>
      <link>https://escholarship.org/uc/item/5262n1mr</link>
      <description>&lt;p&gt;A seven-year-old girl presented to the pediatric emergency department with three days of nonbloody, nonbilious vomiting, nonbloody diarrhea, and decreased oral intake. She also had weight loss and fatigue over the preceding month. The examination showed persistent tachycardia despite antipyretics and fluids. This presentation addresses the many causes of persistent tachycardia in a child with a diagnostic test sent from the emergency department revealing the ultimate diagnosis.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5262n1mr</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Girgis, Mary</name>
      </author>
      <author>
        <name>Stephanos, Kathleen</name>
      </author>
      <author>
        <name>Bontempo, Laura J.</name>
      </author>
      <author>
        <name>Windsor, T. Andrew</name>
        <uri>https://orcid.org/0000-0001-6307-7177</uri>
      </author>
    </item>
    <item>
      <title>Penetrating Neck Injury in a Child Presenting as a Simple Laceration: A Case Report</title>
      <link>https://escholarship.org/uc/item/51d876jf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Penetrating neck injury is rare in children, but it can have devastating consequences due to the vital structures in the neck. Having a high index of suspicion is crucial for detection and management of such injuries. Superficial-appearing wounds can mask underlying injury. In this case report, we present a case of penetrating neck injury in a patient who presented with what appeared to be a simple laceration to his neck.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A three-year-old male presented with a laceration to his neck caused by a piece of shattered glass. On evaluation, he had normal vital signs and no hard or soft signs of penetrating neck injury. During bedside examination, a track was found extending beyond the platysma. The patient developed hoarseness in his voice, prompting computed tomography (CT). The CT revealed three foreign bodies lodged between the right common carotid artery and tracheal wall, abutting the wall. The patient underwent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/51d876jf</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Davitt, Brian</name>
      </author>
      <author>
        <name>Quinn, Eric</name>
      </author>
    </item>
    <item>
      <title>Sorely Mistaken—Soft Palatal Myxedema in Decompensated Hypothyroidism Presenting as a Sore Throat: Case Report</title>
      <link>https://escholarship.org/uc/item/4v42s2gq</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Oropharyngeal myxedema is a rare presenting symptom of decompensated&amp;nbsp;hypothyroidism that can mimic more common causes of sore throat.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We describe a case of an older woman who presented with throat pain and dysphagia,&amp;nbsp;found to have soft palate edema on exam and imaging. Laboratory testing confirmed severe&amp;nbsp;hypothyroidism, and her symptoms eventually resolved with thyroid hormone replacement therapy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;This case highlights a rare and under-recognized presentation of a common&amp;nbsp;endocrine disorder. Consider myxedema from severe hypothyroidism in patients with subacute&amp;nbsp;oropharyngeal pain and swelling. Without early recognition and treatment, the patient is at risk for&amp;nbsp;two life-threatening conditions: airway compromise from soft palate myxedema and progression of&amp;nbsp;hypothyroidism to myxedema coma.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4v42s2gq</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Miller, Gabriella</name>
      </author>
      <author>
        <name>Myers, Bennett A</name>
        <uri>https://orcid.org/0009-0004-1863-3620</uri>
      </author>
    </item>
    <item>
      <title>Blunt Thoracic Aortic Injury Presenting as Hemodynamically Stable: A Case Report</title>
      <link>https://escholarship.org/uc/item/4r85p7bq</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Blunt thoracic aortic injury is a rare but potentially fatal consequence of motor vehicle collisions. While commonly associated with hemodynamic instability, some cases present with normal vital signs, delaying diagnosis and treatment. We present the case of a 42-year-old unrestrained backseat passenger who sustained a blunt thoracic aortic injury following a motor vehicle collision and underwent emergent endovascular repair. This case emphasizes the critical role of early imaging and multidisciplinary coordination in the management of high-risk trauma patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A 42-year-old female presented to the emergency department (ED) following a high-risk motor vehicle collision. She was an unbelted passenger in a vehicle traveling at approximately 35 miles per hour that collided with a telephone pole. The patient was unconscious at the scene but regained consciousness en route. Upon arrival at the ED she was alert,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4r85p7bq</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Knudsen, Joseph</name>
      </author>
      <author>
        <name>Lucas, Stephen</name>
      </author>
      <author>
        <name>Mangano, James</name>
      </author>
    </item>
    <item>
      <title>Berberine Poisoning with Polymorphic Ventricular Tachycardia: A Case Report</title>
      <link>https://escholarship.org/uc/item/4ft5016k</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Natural supplements are readily available without a prescription and are not regulated by the United States Food and Drug Administration. The popularity of berberine, a bioactive compound used for centuries in traditional Chinese medicine, has surged due to its proposed benefits in glycemic control and cardiovascular health. However, use of berberine may lead to possible negative electrophysiologic changes.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 92-year-old male presented to the emergency department (ED) with chief complaints of tremors, urinary incontinence, and brief syncopal episodes that began approximately two weeks after starting berberine. In the ED he had multiple episodes of polymorphic ventricular tachycardia with pulselessness requiring immediate cardioversion, with a rapid return of spontaneous circulation between episodes. Amiodarone was started; however, despite this, he continued to have persistent episodes. Finally, the episodes...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4ft5016k</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Mesmin, Melson P</name>
      </author>
      <author>
        <name>Tweet, Marit S</name>
      </author>
      <author>
        <name>Kim, Sharon H</name>
        <uri>https://orcid.org/0000-0002-8996-9752</uri>
      </author>
      <author>
        <name>Fulks, Tyler J</name>
      </author>
    </item>
    <item>
      <title>Ultrasound-guided Hernia Reduction—Preventing Surgery for an Incarcerated Ventral Hernia: A Case Report</title>
      <link>https://escholarship.org/uc/item/4fc1v72d</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Hernias are a common presenting complaint in the emergency department. If they are not promptly identified and reduced, patients may need urgent surgery, which entails an increase in morbidity and mortality. The diagnosis and reduction of hernias can be challenging due to a patient’s large body habitus. In this case, we demonstrate the utility of using point-of-care ultrasound (POCUS) to detect an abdominal wall defect and provide real-time guidance to reduce a hernia and avoid surgery in a patient who was a poor surgical candidate.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A 48-year-old morbidly obese male with multiple comorbidities presented with abdominal pain at the location of a known ventral hernia. Computed tomography (CT) of the abdomen confirmed a ventral hernia; however, three different physicians attempted reduction and were unsuccessful. We then used POCUS to identify the ventral hernia and the abdominal wall defect and to guide...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4fc1v72d</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lochner, Arion</name>
      </author>
      <author>
        <name>Stovicek, Elizabeth</name>
      </author>
      <author>
        <name>Kman, Nicholas</name>
      </author>
      <author>
        <name>Petelinsek, Sarah</name>
        <uri>https://orcid.org/0009-0005-9733-7674</uri>
      </author>
      <author>
        <name>Cotton, Jennifer</name>
      </author>
    </item>
    <item>
      <title>Emergency Department Presentation of Duloxetine-induced Acute Extrapyramidal Symptoms: A Case Report</title>
      <link>https://escholarship.org/uc/item/4c5952n2</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Duloxetine, a serotonin-norepinephrine reuptake inhibitor, has been associated with extrapyramidal symptoms and tardive syndromes; however, such adverse reactions are rare and remain sparsely documented, particularly in the setting of non-psychiatric use.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A young, healthy, active-duty military service member developed acute extrapyramidal symptoms—restlessness, dystonic movements, and acute dystonia—shortly after initiating duloxetine for postsurgical neuropathic pain.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case highlights the need for vigilance regarding movement disorders in patients prescribed duloxetine, even in the absence of psychiatric comorbidity or antipsychotic exposure.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4c5952n2</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shulby, Michael W.</name>
      </author>
      <author>
        <name>Powell, Christina M.</name>
      </author>
    </item>
    <item>
      <title>Recurrence of Guillain-Barré Syndrome Is not Uncommon, and a Relapse May Require More Aggressive Treatment than the Original Condition</title>
      <link>https://escholarship.org/uc/item/4632c8mb</link>
      <description>Recurrence of Guillain-Barré Syndrome Is not Uncommon, and a Relapse May Require More Aggressive Treatment than the Original Condition</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4632c8mb</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Finsterer, Josef</name>
      </author>
    </item>
    <item>
      <title>Ruptured Abdominal Aortic Aneurysm Identified on Point-of-Care Ultrasound</title>
      <link>https://escholarship.org/uc/item/3vg0r4z5</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation:&lt;/strong&gt; A 78-year-old woman who presented to the emergency department with abdominal pain was found to have a tender, pulsatile abdominal mass on examination. Point-of-care ultrasound demonstrated an abdominal aortic aneurysm with findings concerning for active rupture. Emergent computed tomography angiography confirmed rupture with a large retroperitoneal hematoma.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion: &lt;/strong&gt;Ruptured abdominal aortic aneurysm is a catastrophic diagnosis associated with high mortality, particularly when recognition is delayed. Point-of-care ultrasound is well established for identifying aneurysmal dilation; however, direct visualization of active rupture is rarely described.&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3vg0r4z5</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sherman, Michael</name>
      </author>
    </item>
    <item>
      <title>Misplaced Central Venous Catheter Leading to a Chemothorax: Case Report</title>
      <link>https://escholarship.org/uc/item/3km0945p</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The placement of central venous catheters (CVC) is a common procedure for the administration of chemotherapy. Adverse events include malposition or displacement; there are limited reports of misplaced implanted CVCs.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 59-year-old female with a history of recently diagnosed metastatic small cell lung cancer, hypertension, former tobacco use of over 60 pack-years, and chronic obstructive pulmonary disease without chronic hypoxemic respiratory failure presented to the emergency department following the first outpatient infusion of chemotherapy. She developed acute onset dyspnea, moderate respiratory distress, and hypoxemia. She was found to have a malpositioned subclavian implanted (ie, “port”) CVC that was placed under fluoroscopy the week prior with placement confirmed by chest radiograph. The evaluation revealed a large right pleural effusion secondary to unintentional intrapleural infusion of chemotherapy....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3km0945p</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Miller, Hannah E.</name>
        <uri>https://orcid.org/0000-0002-0541-1939</uri>
      </author>
      <author>
        <name>Lentz, Skyler</name>
      </author>
    </item>
    <item>
      <title>Unmasking the Silent Liver-Lung Connection: A Pediatric Hepatopulmonary Syndrome Case Report</title>
      <link>https://escholarship.org/uc/item/3js6z7z5</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Hepatopulmonary syndrome is a rare but serious cause of pediatric hypoxemia.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 10-year-old obese male with obstructive sleep apnea and asthma presented to the emergency department with low baseline oxygen saturations and exertional hypoxia, despite normal physical exam and outpatient pulmonary function testing. Workup revealed liver cirrhosis, hepatosplenomegaly, gastroesophageal varices, and an elevated alveolar-arterial gradient, raising concern for hepatopulmonary syndrome. He was diagnosed with this disease at a tertiary hepatology center and underwent liver transplantation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&amp;nbsp;&lt;/strong&gt;Emergency physicians should consider hepatopulmonary syndrome in children with unexplained hypoxia and liver disease, especially in a child with a normal lung exam and no bronchodilator response.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3js6z7z5</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Haupt, Shawn A.</name>
      </author>
      <author>
        <name>Lalos, Demetra</name>
      </author>
      <author>
        <name>Muntean, Cornelia</name>
      </author>
      <author>
        <name>Vaysman, Dmitriy</name>
      </author>
    </item>
    <item>
      <title>Transaminitis from Duloxetine: Case Report</title>
      <link>https://escholarship.org/uc/item/3607s65c</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Duloxetine, a serotonin-norepinephrine reuptake inhibitor, is commonly prescribed for depression, anxiety, and neuropathic pain. Although rare, duloxetine has been associated with hepatotoxicity.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present the case of a 61-year-old male with multiple comorbidities who developed significant transaminitis two months after initiation of duloxetine therapy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Emergency physicians should be cognizant of duloxetine-induced liver injury, particularly in patients with increased risk factors who present with unexplained liver injury.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3607s65c</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Galletta, Gayle</name>
      </author>
      <author>
        <name>Mehta, Savant</name>
      </author>
      <author>
        <name>Jancura, Daniel</name>
      </author>
      <author>
        <name>Ryan, Daminica</name>
      </author>
      <author>
        <name>Li, Irene</name>
      </author>
    </item>
    <item>
      <title>Persistent and Progressive Exfoliative Dermatitis: A Case Report</title>
      <link>https://escholarship.org/uc/item/34x717qk</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Exfoliative dermatitis, also known as erythroderma, represents an infrequent clinical presentation in emergency departments (ED) and often contributes to considerable diagnostic uncertainty. The differential diagnosis is broad, and the condition may arise from a wide variety of etiologies. We report a case of severe exfoliative dermatitis characterized by gradual progression and resistance to multiple therapeutic interventions over several weeks, ultimately resulting in significant systemic complications and marked hematological abnormalities.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 57-year-old man presented to the ED with severe pain, pruritus, and widespread skin peeling involving more than 90% of his body surface area. The patient developed a rash following a trip to Korea about six months prior to presentation, which progressively worsened despite multiple prior diagnoses and treatments including corticosteroids, immunosuppressive therapy,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/34x717qk</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Boukouris, Jennifer</name>
        <uri>https://orcid.org/0009-0001-2349-7203</uri>
      </author>
      <author>
        <name>Elsherif, Sherif</name>
        <uri>https://orcid.org/0009000834650032</uri>
      </author>
    </item>
    <item>
      <title>Incidental Diagnosis of ST-Elevation Myocardial Infarction on Computed Tomography in a Burn Patient: A Case Report</title>
      <link>https://escholarship.org/uc/item/2xb7r5tg</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;ST-elevation myocardial infarctions (STEMI) represent complete occlusion of a coronary artery. An electrocardiogram (ECG) is a method of diagnosis; however, on rare occasions clues of myocardial infarction are first noted on imaging. This is a case of myocardial infarction first noted on computed tomography (CT).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A 62-year-old man was brought to the emergency department after being found unresponsive with multiple burns. An ECG performed on arrival did not show changes consistent with myocardial ischemia. Due to reported trauma, a CT incidentally found a heterogeneous low-attenuation area in the posterior wall of the left ventricle of the heart. A repeat ECG subsequently showed an inferior STEMI.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; Computed tomography of the chest obtained in the evaluation of trauma may demonstrate evidence of myocardial ischemia. This case highlights the ability of CT to detect...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2xb7r5tg</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Araujo, Maria Jose</name>
      </author>
      <author>
        <name>Sandhu, Eknoor</name>
        <uri>https://orcid.org/0009-0001-9258-890X</uri>
      </author>
      <author>
        <name>Romero, Angel</name>
      </author>
      <author>
        <name>Randhawa, Jugraj</name>
        <uri>https://orcid.org/0009-0000-7235-8659</uri>
      </author>
      <author>
        <name>O’Donnell, Rachel</name>
      </author>
    </item>
    <item>
      <title>Non-traumatic First Rib Fracture in a Young Weightlifter Resulting in Winged Scapula: A Case Report</title>
      <link>https://escholarship.org/uc/item/2w7697n7</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Shoulder pain is a common emergency department (ED) presentation. Scapular&amp;nbsp;winging is a rare condition often associated with long thoracic nerve injury.&amp;nbsp;This case report&amp;nbsp;describes an even rarer case of dorsal scapular nerve injury caused by a nontraumatic first rib&amp;nbsp;fracture in a young weightlifter, an injury mechanism not previously reported in the literature.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 17-year-old male presented to the ED with left shoulder pain following weightlifting.&amp;nbsp;Physical examination demonstrated scapular winging, and a clinical diagnosis of dorsal scapular&amp;nbsp;neuropraxia was made. Imaging revealed a nontraumatic first rib fracture.&amp;nbsp;The patient was treated&amp;nbsp;conservatively with nonsteroidal anti-inflammatory drugs and rest, resulting in complete resolution of&amp;nbsp;symptoms within two weeks at clinic follow-up.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;To our knowledge, this is the first case...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2w7697n7</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Remy, Jessica</name>
      </author>
      <author>
        <name>Prendergast, Nicole</name>
      </author>
    </item>
    <item>
      <title>The Floating Threat: A Rare Case Report of Carotid Saddle&amp;nbsp;Thrombus in a Healthy Adult</title>
      <link>https://escholarship.org/uc/item/2tc110vg</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Carotid free-floating thrombus is a rare and potentially devastating cause of ischemic stroke. Diagnosis remains challenging due to the dynamic nature of the lesion.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;:&amp;nbsp;We report the case of a 46-year-old female presenting with neck pressure and gait&amp;nbsp;instability, who was found to have a free-floating thrombus at the brachiocephalic-carotid junction.&amp;nbsp;Despite early anticoagulation, she developed biparietal ischemic strokes.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;This case highlights the challenges in management of carotid free-floating thrombus&amp;nbsp;including appropriate anticoagulation, contraindications to thrombolysis, and the need for&amp;nbsp;multidisciplinary involvement. Emergency physicians must maintain high suspicion for vascular&amp;nbsp;pathology in atypical neurologic presentations and recognize that even optimal medical therapy does&amp;nbsp;not eliminate stroke risk.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2tc110vg</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Droger, Ariel</name>
      </author>
      <author>
        <name>Torres-Castro, Rolando</name>
        <uri>https://orcid.org/0009-0009-9976-672X</uri>
      </author>
      <author>
        <name>Mahmood, Kashan</name>
      </author>
      <author>
        <name>Graf, Jason</name>
      </author>
      <author>
        <name>Serio, Sean</name>
      </author>
      <author>
        <name>Scumpia, Alexander John</name>
        <uri>https://orcid.org/0000-0001-6862-6315</uri>
      </author>
    </item>
    <item>
      <title>Novel Technique in Performing Ocular Ultrasound in Trauma: A Case Series</title>
      <link>https://escholarship.org/uc/item/2bj3g0pr</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Ocular ultrasound is highly effective for diagnosing traumatic eye injuries such as retinal detachment, vitreous hemorrhage, foreign bodies, and retrobulbar hematomas. However, it is contraindicated in cases of suspected globe rupture, as applying external pressure to the eye could cause further damage. When globe injury is clinically suspected, computed tomography is typically used to confirm the diagnosis. However, delays can occur if other life-threatening injuries require immediate attention or there are long wait times. We propose a novel method for performing ocular ultrasound in such cases—the modified water bath technique—which allows for the diagnosis of globe rupture upon the patient’s arrival in the emergency department.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series:&lt;/strong&gt; We present five cases where the modified water bath technique was used. A glove partially filled with saline is prepared and gently placed on the affected eye while the patient lies...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2bj3g0pr</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chawang, Hannah</name>
        <uri>https://orcid.org/0000-0003-2158-2065</uri>
      </author>
      <author>
        <name>Bhoi, Sanjeev</name>
      </author>
      <author>
        <name>Chandran, Vineeth</name>
      </author>
      <author>
        <name>Chanda, Anmol</name>
      </author>
      <author>
        <name>Das, Anand Kumar</name>
      </author>
    </item>
    <item>
      <title>Implementation of a Novel Agitated Behavior Score and Its Association with Code Violet Activation: A Case Series</title>
      <link>https://escholarship.org/uc/item/28v7b6tn</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Agitation in the emergency department (ED) poses a significant safety concern for staff and patients. Multidisciplinary responses, such as Code Violet activations, are common but resource-intensive. Early identification and intervention may reduce escalation, but ED-specific data are limited. The objective of the study was to evaluate the implementation of a novel agitated behavior score (ABS) and assess whether higher ABS scores are associated with increased risk of Code Violet activation.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series:&lt;/strong&gt; This prospective observational study included adult patients admitted to a behavioral health unit in a community teaching hospital ED. Trained staff administered a novel 25-point ABS incorporating altered mentation, verbal agitation, and motor agitation. The primary outcome was Code Violet activation; secondary outcomes included pharmacologic interventions and substance use. Among 83 patients, 27 (33%) experienced ≥ 1 Code...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28v7b6tn</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ceraolo, Negin</name>
      </author>
      <author>
        <name>Sandine, Julianna</name>
      </author>
      <author>
        <name>Crouse, Bethany</name>
      </author>
      <author>
        <name>Krizo, Jessica</name>
      </author>
      <author>
        <name>Simon, Erin L</name>
      </author>
    </item>
    <item>
      <title>Emergency Department Transvenous Pacemaker Placement Complicated by Tricuspid Mass</title>
      <link>https://escholarship.org/uc/item/22j4p7w7</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;Temporary transvenous pacemaker placement is frequently performed in&amp;nbsp;the emergency department for the management of symptomatic bradyarrhythmias. We report the&amp;nbsp;case of a 93-year-old male who presented with profound bradycardia, hypotension, and altered&amp;nbsp;mental status requiring emergent pacing. Initial transcutaneous pacing achieved hemodynamic&amp;nbsp;improvement but necessitated escalation to transvenous pacing due to patient discomfort and&amp;nbsp;high current requirements. During attempted transvenous pacemaker placement, resistance&amp;nbsp;was encountered and capture could not be achieved despite appropriate technique. Subsequent&amp;nbsp;cardiology consultation and imaging revealed an undiagnosed tricuspid valve myxoma obstructing&amp;nbsp;catheter advancement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;: This case highlights a rare mechanical complication of transvenous pacemaker&amp;nbsp;placement caused by an intracardiac mass. Awareness of structural...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/22j4p7w7</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Molyneux, Kevin</name>
      </author>
      <author>
        <name>Krejchi, Nicholas</name>
      </author>
      <author>
        <name>Fulton II, Matthew Robert</name>
      </author>
      <author>
        <name>Youssef, Mina</name>
      </author>
    </item>
    <item>
      <title>Immunoglobulin A Vasculitis-Associated Ileoileal Intussusception in an Adult Male: Case Report</title>
      <link>https://escholarship.org/uc/item/1vr3s5k2</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Immunoglobulin A (IgA) vasculitis, formerly known as Henoch–Schönlein purpura, is a small-vessel leukocytoclastic vasculitis caused by IgA immune complex deposition. While it is the most common systemic vasculitis in children, adult cases can present with more severe systemic manifestations. The classic clinical tetrad includes palpable purpura, arthralgia, abdominal pain, and renal involvement. Gastrointestinal symptoms, occurring in approximately two-thirds of cases, result from inflammation of small bowel vessels resulting in bowel wall edema and hemorrhage, which may serve as lead points for intussusception.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; A 21-year-old male presented with two days of severe periumbilical abdominal pain, bilateral knee pain, and a nonblanching palpable purpuric rash on his lower extremities. Physical examination revealed a soft but tender abdomen. Lab results were remarkable for leukocytosis. Computed tomography (CT)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1vr3s5k2</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sawhney, Preet</name>
      </author>
      <author>
        <name>Frost, Patrick</name>
      </author>
      <author>
        <name>Stueve, Peter</name>
      </author>
      <author>
        <name>Boccio, Eric</name>
      </author>
    </item>
    <item>
      <title>A Diagnostic Pitfall in the Emergency Department —Aortic Dissection Masquerading as Acute Paraplegia: A Case Report</title>
      <link>https://escholarship.org/uc/item/1vb4c5q0</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acute aortic dissection is a life-threatening emergency with a wide spectrum of clinical presentations. Neurological deficits as the initial manifestation of aortic dissection are uncommon and may result in delayed or missed diagnosis. This case describes aortic dissection presenting primarily as acute paraplegia without persistent chest pain or other classic features.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report a 52-year-old male who presented with sudden-onset paraplegia. Neurological examination revealed flaccid paralysis of both lower limbs, with loss of pain and temperature sensation below the first lumbar dermatome and preserved dorsal column modalities. The patient was hypertensive on presentation. A clinical diagnosis of anterior spinal artery syndrome was made. Contrast-enhanced computed tomography of the chest and abdomen demonstrated a Stanford type A aortic dissection. The patient was counseled regarding the need for urgent surgical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1vb4c5q0</guid>
      <pubDate>Wed, 12 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Nagarajan, Sindujaa</name>
      </author>
      <author>
        <name>Ganessane, Ezhilkugan</name>
        <uri>https://orcid.org/0000-0001-8541-5675</uri>
      </author>
      <author>
        <name>B G, Kowsthubha</name>
        <uri>https://orcid.org/0009-0006-7909-7248</uri>
      </author>
      <author>
        <name>Somasundaram, Anukarthika</name>
      </author>
      <author>
        <name>Balamurugan, Nathan</name>
      </author>
    </item>
  </channel>
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