<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:atom="http://www.w3.org/2005/Atom" version="2.0">
  <channel>
    <docs>http://www.rssboard.org/rss-specification</docs>
    <atom:link rel="self" type="application/rss+xml" href="https://escholarship.org/uc/uciem_cpcem/rss"/>
    <ttl>720</ttl>
    <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, 3 Aug 2026 17:27:57 +0000</pubDate>
    <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, 29 Jul 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>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>Tue, 28 Jul 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>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>Tue, 28 Jul 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>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>Tue, 28 Jul 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ball, Seth</name>
      </author>
      <author>
        <name>Wierzbicki, Marissa</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>Tue, 28 Jul 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>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>Mon, 20 Jul 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>Mon, 20 Jul 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sakamoto, So</name>
        <uri>https://orcid.org/0000-0002-0921-7375</uri>
      </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>Mon, 20 Jul 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>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>Mon, 20 Jul 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>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>Mon, 20 Jul 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>Stridor and Dysphagia Unmasking an Aberrant Right Subclavian Artery in a Toddler</title>
      <link>https://escholarship.org/uc/item/1ct7231h</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation:&lt;/strong&gt; A one-year-old girl presented with acute-onset dyspnea persistent for two days and recurrent choking episodes. Physical examination revealed stridor and sub-costal retractions. Despite initial treatment with inhaled nebulized epinephrine, stridor persisted. Lateral chest radiography finding indicated tracheal stenosis. Contrast-enhanced neck and chest computed tomography (CT) showed an aberrant right subclavian artery compressing the esophagus posteriorly, causing esophageal stenosis with associated food residue accumulation. The proximally dilated portion of the esophagus caused mass effect with compression of the trachea, resulting in tracheal stenosis. Despite medical management, the patient experienced recurrent stridor and could only swallow liquids. Therefore, surgical translocation of the right subclavian artery to the right common carotid artery was performed. Postoperatively, the patient swallowed age-appropriate food, and the stridor...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ct7231h</guid>
      <pubDate>Mon, 20 Jul 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yasuda, Masato</name>
      </author>
      <author>
        <name>Ito, Tomoya</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>Fri, 10 Jul 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>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>Fri, 10 Jul 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>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>Fri, 10 Jul 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>Fri, 10 Jul 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Finsterer, Josef</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>Fri, 10 Jul 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>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>Mon, 29 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Marquis, Taylor</name>
      </author>
      <author>
        <name>Sheng, Alexander Y</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>Mon, 29 Jun 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>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>Mon, 29 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sherman, Michael</name>
      </author>
    </item>
    <item>
      <title>&amp;nbsp;Severe Tetanus Following a Rooster-Peck Injury Requiring Nasotracheal Intubation: A Case Report</title>
      <link>https://escholarship.org/uc/item/1mz494sf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Tetanus is a rare but life-threatening disease caused by Clostridium tetani, characterized by generalized muscle rigidity, autonomic instability, and respiratory compromise.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We present a case of a 65-year-old male poultry hobbyist with type two diabetes who developed severe tetanus following a rooster-peck injury to his finger. The patient presented with progressive trismus and respiratory distress necessitating fiberoptic nasotracheal intubation and subsequent tracheostomy. Despite appropriate antimicrobial therapy, immunoglobulin administration, and sedation, the patient continued to exhibit spasms when sedation was reduced.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&amp;nbsp;&lt;/strong&gt;This case highlights the ongoing risk of tetanus in under-immunized agricultural populations, the challenges of airway management in severe trismus, and the importance of maintaining vaccination awareness even in developed healthcare...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1mz494sf</guid>
      <pubDate>Mon, 29 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>White, Robin</name>
        <uri>https://orcid.org/0009-0008-0813-0850</uri>
      </author>
      <author>
        <name>Singh, Hardeep</name>
      </author>
      <author>
        <name>Craver, Kelsey</name>
      </author>
      <author>
        <name>Cranston, Rebecca</name>
      </author>
      <author>
        <name>Hodge, Kelsey</name>
      </author>
      <author>
        <name>Vandervort, Elizabeth</name>
      </author>
    </item>
    <item>
      <title>Keeping An Eye Out for Stroke—Herpes Zoster Ophthalmicus Leading to Acute Ischemic Stroke</title>
      <link>https://escholarship.org/uc/item/0vc4j8xs</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Herpes zoster ophthalmicus, a reactivation of varicella-zoster virus involving the ophthalmic branch of the trigeminal nerve, is a known but under-recognized risk factor for acute cerebrovascular and cardiovascular events.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of an 84-year-old female with herpes zoster ophthalmicus who suffered a fatal ischemic stroke and bilateral submassive pulmonary emboli within days of diagnosis. Despite early identification and appropriate antiviral treatment, the patient experienced rapid neurological decline and ultimately succumbed to complications.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; This case underscores the critical association between herpes zoster ophthalmicus and increased risk of stroke and myocardial infarction, as supported by growing epidemiologic evidence. Physicians should be aware of these severe complications, consider close monitoring and cardiovascular risk stratification...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0vc4j8xs</guid>
      <pubDate>Mon, 29 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Burke, Summer</name>
      </author>
      <author>
        <name>Armbruster, Mary</name>
      </author>
      <author>
        <name>Le, Jacqueline</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>Sun, 28 Jun 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>Sat, 27 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Golder, Jack</name>
      </author>
      <author>
        <name>Tjiattas-Saleski, Lindsay</name>
      </author>
    </item>
    <item>
      <title>Cerebral Kounis Syndrome—A Rare Case Report of Cerebral Vasospasm Following Anaphylaxis</title>
      <link>https://escholarship.org/uc/item/1dg7k0mw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Kounis syndrome describes anaphylaxis-induced coronary vasospasm and is often misdiagnosed as acute coronary syndrome. We report a similar phenomenon of cerebral vasospasm following anaphylaxis, a rare and under-recognized mimic of stroke.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp;&lt;/strong&gt;A previously healthy 45-year-old gentleman developed sudden right-sided hemiparesis and dysarthria while working outdoors, accompanied by generalized pruritus, rash, presyncope, dyspnea, palpitation, and abdominal pain. He received prompt intramuscular epinephrine and other anti-inflammatory agents, resulting in rapid symptom resolution and complete recovery in the emergency department. Computed tomography of the brain and other studies were unremarkable. This case underscores a rare neurological manifestation of anaphylaxis.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion:&amp;nbsp;&lt;/strong&gt;Cerebral vasospasm is an unusual sequela of anaphylaxis that may lead to a diagnostic dilemma. Prompt...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1dg7k0mw</guid>
      <pubDate>Sat, 27 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ismail, Mohd Helmie</name>
        <uri>https://orcid.org/0000-0002-1890-5233</uri>
      </author>
      <author>
        <name>Muniandy, Sadesvaran</name>
      </author>
      <author>
        <name>Azmi, Muhammad Shafiq</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>Fri, 26 Jun 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>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>Fri, 26 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Davitt, Brian</name>
      </author>
      <author>
        <name>Quinn, Eric</name>
      </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>Thu, 25 Jun 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>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>Mon, 25 May 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>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>Sat, 23 May 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>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>Sat, 23 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Offman, Ryan</name>
      </author>
      <author>
        <name>Baribeau, Sarah K</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>Sat, 23 May 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>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>Sat, 23 May 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>A Split from Traditional Orbital Compartment Syndrome&amp;nbsp;Intervention: Case Report of Vision-saving Vertical Lid&amp;nbsp;Split Procedure</title>
      <link>https://escholarship.org/uc/item/12r398jz</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Many emergency physicians will never perform a lateral canthotomy and cantholysis, and one-third of those who try will be unsuccessful at relieving the pressure that threatens&amp;nbsp; permanent vision loss. This procedure is notoriously difficult and rare, but a recently proposed&amp;nbsp;alternative—the vertical lid split—may be simpler and more effective.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We report the case of a 35-year-old woman with motor vehicle collision-related orbital trauma&amp;nbsp;who presented to a community emergency department. Initially, she had intact vision and extraocular&amp;nbsp;movements. Imaging showed a comminuted inferior orbital blowout fracture with retrobulbar hemorrhage,&amp;nbsp;and the transfer process was initiated. However, after coughing she developed vision loss and elevated&amp;nbsp;intraocular pressure. Lateral canthotomy and cantholysis was performed for suspected orbital compartment&amp;nbsp;syndrome but did not fully address the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/12r398jz</guid>
      <pubDate>Sat, 23 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chason, Hannah</name>
        <uri>https://orcid.org/0000-0003-1771-9479</uri>
      </author>
      <author>
        <name>Zimmerman, Barret</name>
      </author>
      <author>
        <name>Jenzer, Andrew</name>
      </author>
      <author>
        <name>Fay, David</name>
      </author>
      <author>
        <name>Elpers, Julia</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, 29 Apr 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>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, 29 Apr 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>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, 29 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Remy, Jessica</name>
      </author>
      <author>
        <name>Prendergast, Nicole</name>
      </author>
    </item>
    <item>
      <title>An Unusual Case of Spontaneous Pneumothorax Presenting as&amp;nbsp;Right Lower Quadrant Pain: A Case Report</title>
      <link>https://escholarship.org/uc/item/13x391fq</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Primary spontaneous pneumothorax generally presents with symptoms of chest pain&amp;nbsp;and shortness of breath. Progression to a tension pneumothorax results in a medical emergency.&amp;nbsp;Rare presentations with abdominal pain are possible and must be considered to expedite&amp;nbsp;appropriate treatment of pneumothorax.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We report a case of a 21-year-old male with primary spontaneous pneumothorax&amp;nbsp;who initially presented to the emergency department with right lower quadrant abdominal pain.&amp;nbsp;History and physical exam were suggestive of acute appendicitis. A large right pneumothorax was incidentally found on computed tomography.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;This case highlights unusual presentations of pneumothorax. Emergency physicians&amp;nbsp;should consider atypical presentations of chest pathology such as pneumothorax in patients&amp;nbsp;presenting with symptoms consistent with an acute abdomen.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/13x391fq</guid>
      <pubDate>Wed, 29 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Crowe, Timothy</name>
      </author>
      <author>
        <name>Cheatle, Patrick</name>
      </author>
    </item>
    <item>
      <title>Electrocardiographic Changes Related to Targeted Temperature Management in Brugada Syndrome: A Case Report</title>
      <link>https://escholarship.org/uc/item/1120q3v9</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Brugada syndrome is an important differential diagnosis for unexplained sudden&amp;nbsp;cardiac arrest, particularly in younger patients. The electrocardiographic (ECG) pattern characteristic&amp;nbsp;of Brugada syndrome can be provoked by fever and may vary with changes in body temperature.&amp;nbsp;Therefore, targeted temperature management following cardiac arrest may obscure the distinctive&amp;nbsp;morphology, increasing the risk of misdiagnosis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&lt;/strong&gt; We report the case of a 44-year-old man who experienced out-of-hospital cardiac arrest due to ventricular fibrillation following influenza B infection. Initial evaluation revealed transient ST-segment elevation in leads V1-V3, while coronary angiography and echocardiographic findings were normal. Although Brugada syndrome was suspected, the diagnosis was deferred because the ECG findings normalized during targeted temperature management at 36°Celsius. However, after completion...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1120q3v9</guid>
      <pubDate>Wed, 29 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kondo, Yuki</name>
        <uri>https://orcid.org/0000-0003-1270-8308</uri>
      </author>
      <author>
        <name>Tanaka, Atsuhito</name>
      </author>
      <author>
        <name>Okazaki, Tomoya</name>
      </author>
    </item>
    <item>
      <title>Pneumocephalus Secondary to Sternutation: A Case Report</title>
      <link>https://escholarship.org/uc/item/9r8461ds</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Sternutation is a physiological reflex that clears the upper respiratory tract through forceful air expulsion. Although it is typically considered benign, sternutation can generate&amp;nbsp;substantial pressure and airflow that can result in barotrauma, including pneumocephalus.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 67-year-old female presented with shortness of breath, rhinorrhea, and a headache&amp;nbsp;following sneezing. Physical exam revealed no signs of trauma or neurological deficits but did note&amp;nbsp;clear rhinorrhea bilaterally. Computed tomography (CT) of the head revealed extensive extra-axial&amp;nbsp;intracranial gas bilaterally, and the patient was admitted for further management. While admitted,&amp;nbsp;otolaryngology was consulted and surgically corrected a right cribriform meningoencephalocele with&amp;nbsp;an active cerebrospinal fluid leak. At follow-up the patient had no residual rhinorrhea symptoms or&amp;nbsp;focal neurological findings.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;One...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9r8461ds</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tejpal, Tushar</name>
      </author>
      <author>
        <name>Ashurst, John</name>
      </author>
      <author>
        <name>Barnett-Trapp, Danielle</name>
      </author>
    </item>
    <item>
      <title>Ventricular Tachycardia Following Kratom Ingestion&amp;nbsp;Requiring Extracorporeal Membrane Oxygenation in a Young&amp;nbsp;Woman: Case Report</title>
      <link>https://escholarship.org/uc/item/9r43b2xz</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Kratom (&lt;em&gt;Mitragyna speciosa&lt;/em&gt;) is an unregulated herbal supplement increasingly&amp;nbsp;associated with severe toxicity. Concentrated liquid formulations pose risks, with emerging reports of&amp;nbsp;seizures, hepatotoxicity, and arrhythmias.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Case Report:&lt;/strong&gt;A previously healthy 24-year-old woman ingested a highly concentrated kratom&amp;nbsp;extract and developed seizure-like activity followed by pulseless monomorphic ventricular&amp;nbsp;tachycardia. She underwent approximately 45 minutes of resuscitation, including multiple&amp;nbsp;defibrillations, dual-sequential shocks, amiodarone, lidocaine, magnesium, calcium, sodium&amp;nbsp;bicarbonate, potassium repletion, epinephrine, and esmolol. Persistent instability prompted&amp;nbsp;consultation with cardiology and cardiothoracic surgery, and she was cannulated for venoarterial&amp;nbsp;extracorporeal membrane oxygenation (ECMO) in the emergency department. Lab studies showed&amp;nbsp;profound hypokalemia,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9r43b2xz</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Mclin-Evans, Megan</name>
      </author>
      <author>
        <name>Tiscareno, Jennerfer</name>
      </author>
      <author>
        <name>Beneke, Laura Lee</name>
      </author>
    </item>
    <item>
      <title>Point-of-Care Ultrasound After Non-fatal Drowning in Rural&amp;nbsp;Western Nepal: A Case Report</title>
      <link>https://escholarship.org/uc/item/9h01z918</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Drowning is a significant cause of death in Nepal, especially in rural areas. Identifying&amp;nbsp;pulmonary edema is important for management of cases of non-fatal drowning, and while radiograph&amp;nbsp;is the standard of care, point-of-care ultrasound (POCUS) offers a rapid, accessible alternative.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 40-year-old woman presented to the emergency department after non-fatal&amp;nbsp;drowning with respiratory distress and hypoxia. Chest radiograph was unavailable. Point-of-care&amp;nbsp;ultrasound revealed diffuse B-lines consistent with pulmonary edema. She was stabilized and&amp;nbsp;transported to a hospital with intensive care-level management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;Point-of-care ultrasound enabled rapid identification of pulmonary edema and guided&amp;nbsp;timely referral. In resource-limited settings, POCUS is a valuable tool for managing drowning victims&amp;nbsp;when other diagnostics are unavailable.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9h01z918</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kansakar, Rochak</name>
      </author>
      <author>
        <name>Katz, Elijah J</name>
      </author>
      <author>
        <name>Zhao, Justin</name>
      </author>
      <author>
        <name>Weldon, Evan</name>
      </author>
    </item>
    <item>
      <title>Meningococcemia in a Boy with Dense Deposit Disease Receiving&amp;nbsp;the C5 Complement Inhibitor Ravulizumab: A Case Report</title>
      <link>https://escholarship.org/uc/item/85z10556</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Dense deposit disease, also known as C3 glomerulopathy, is a rare renal disorder&amp;nbsp;caused by abnormal complement deposition in the glomerular basement membrane. Patients often&amp;nbsp;require long-term immunosuppressive therapy and, in some cases, complement inhibitors such as&amp;nbsp;ravulizumab. While effective at limiting renal damage, complement blockade significantly increases&amp;nbsp;susceptibility to invasive infections from encapsulated bacteria, particularly&amp;nbsp;&lt;em&gt;Neisseria meningitidis&lt;/em&gt;.&amp;nbsp;Despite immunization and antimicrobial prophylaxis, these patients remain incompletely protected.&amp;nbsp;We describe a case of meningococcemia in a fully vaccinated adolescent with dense deposit&amp;nbsp;disease on ravulizumab therapy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 17-year-old male with a history of dense deposit disease on mycophenolate mofetil and ravulizumab presented to the pediatric emergency department with fever, vomiting, altered...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/85z10556</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gonedes, Andrew</name>
      </author>
      <author>
        <name>Martinez, Alexandra</name>
      </author>
      <author>
        <name>Greissman, Allan M.</name>
      </author>
      <author>
        <name>Atia, Hanan</name>
      </author>
      <author>
        <name>Boccio, Eric</name>
      </author>
    </item>
    <item>
      <title>Reversible Cerebral Vasoconstriction Syndrome Following a&amp;nbsp;Steroid Burst: A Case Report</title>
      <link>https://escholarship.org/uc/item/82w848j0</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Reversible cerebral vasoconstriction syndrome is a recently defined disease entity&amp;nbsp;classically presenting with recurrent thunderclap headache. The pathology involves triggered cerebral&amp;nbsp;arterial vasoconstriction, which can lead to complications including seizure, ischemic stroke, and&amp;nbsp;intracranial hemorrhage. Diagnosis requires angiography, and treatment consists of vasodilatory therapy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We describe a case of reversible cerebral vasoconstriction syndrome following&amp;nbsp;glucocorticoid burst therapy in a patient on multiple vasoactive medications, suggesting the&amp;nbsp;possibility of compounding risk factors and triggers. As is common with this syndrome, the patient in&amp;nbsp;our case required multiple hospital visits for diagnosis but ultimately experienced a positive outcome&amp;nbsp;upon treatment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;The presentation of reversible cerebral vasoconstriction syndrome...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/82w848j0</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lenning, Jacob</name>
      </author>
      <author>
        <name>Halfill, Caleb</name>
      </author>
      <author>
        <name>Rountree, Justin</name>
      </author>
    </item>
    <item>
      <title>Atrial Fibrillation in a Young Patient Using High-dose Oral&amp;nbsp;Diclofenac: A Case Report</title>
      <link>https://escholarship.org/uc/item/7p89z6dp</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Diclofenac sodium is a widely used medication for its analgesic and anti-inflammatory properties. Although the adverse effects of diclofenac are well described, diclofenac-associated new-onset atrial fibrillation in a young, healthy adult has not been previously reported.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 22-year-old man with severe pain following an ankle injury used diclofenac sodium&amp;nbsp;at a dose of 50 mg orally three times daily for one week. At the end of the week, he presented to the&amp;nbsp;emergency department (ED) complaining of palpitations for a few hours. The patient had no past&amp;nbsp;medical history. His physical examination revealed no pathologic signs except for tachycardia and&amp;nbsp;an irregularly irregular pulse rate. An electrocardiogram showed an irregularly irregular rhythm with&amp;nbsp;a ventricular rate of 128 beats per minute (bpm) (rapid ventricular response) and absent P waves,&amp;nbsp;consistent with atrial fibrillation. The...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7p89z6dp</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Çağlar, Sabri Onur</name>
      </author>
      <author>
        <name>Çağlar, Hilal</name>
      </author>
      <author>
        <name>Hira, Serdar</name>
      </author>
    </item>
    <item>
      <title>19-month-old Girl with Seizure</title>
      <link>https://escholarship.org/uc/item/7mb8k87q</link>
      <description>&lt;p&gt;Pediatric seizures are an alarming presentation to the emergency department (ED) that can be&amp;nbsp;caused by a multitude of etiologies. It is important to differentiate life-threatening conditions from&amp;nbsp;more benign causes. A 19-month-old girl presented to the ED after a witnessed seizure. This case&amp;nbsp;offers a differential diagnosis for pediatric seizures and uses history, exam, laboratory findings, and&amp;nbsp;imaging to hone the differential in the ED setting. The surprising final diagnosis and case outcome&lt;br&gt;are then revealed and discussed.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7mb8k87q</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kurek, Julie</name>
      </author>
      <author>
        <name>Falat, Cheyenne</name>
      </author>
      <author>
        <name>Bontempo, Laura J</name>
      </author>
      <author>
        <name>Gatz, John David</name>
        <uri>https://orcid.org/0000-0002-3380-2419</uri>
      </author>
    </item>
    <item>
      <title>Minimally Symptomatic Severe Hyponatremia: Two Case Reports</title>
      <link>https://escholarship.org/uc/item/6j41d4bw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Hyponatremia is a common and often vexing electrolyte abnormality seen in&amp;nbsp;the emergency setting. The severity of a patient’s symptoms is often dictated by the acuity of&amp;nbsp;hyponatremia development and degree of serum sodium deficit, with patients typically demonstrating&amp;nbsp;more severe neurological symptoms in acute-onset severe hyponatremia. Patients prescribed&amp;nbsp;chlorthalidone are at particular risk of developing hyponatremia, especially in the setting of a&amp;nbsp;secondary insult.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: We describe two patients presenting to the emergency department with severe&amp;nbsp;hyponatremia who were taking chlorthalidone. Both patients had clinical symptoms that were mild&amp;nbsp;given the degree of their hyponatremia. Additionally, each patient had a secondary insult affecting&amp;nbsp;their volume status that was an important contributing factor in the development of hyponatremia.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: Thiazide...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6j41d4bw</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Richardson, Jordan</name>
      </author>
      <author>
        <name>Wood, Luke</name>
      </author>
      <author>
        <name>Raukar, Neha</name>
      </author>
    </item>
    <item>
      <title>Central Retinal Artery Occlusion Diagnosed via Ocular Point-of-care Ultrasound: Case Report</title>
      <link>https://escholarship.org/uc/item/5wv73358</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Central retinal artery occlusion (CRAO) is a neurological and ophthalmologic&amp;nbsp;emergency that presents as sudden, painless, monocular vision loss. Central retinal artery occlusioncan be classified as arteritic or non-arteritic. Most cases of non-arteritic CRAO are due to embolism,&amp;nbsp;commonly from atherosclerosis of the ipsilateral carotid artery. More proximal sources of embolism&amp;nbsp;are uncommon but can occur. Prompt recognition of CRAO is critical for vision preservation therapy&amp;nbsp;and initiation of ischemic stroke diagnosis protocols.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: We present the case of a 66-year-old female who presented to the emergency department eight hours after sudden, painless, monocular vision loss. Her past medical history included type II diabetes, hypertension, and hyperlipidemia. She had previously undergone bilateral lens replacement for cataracts three years prior and had a history of intermittent floaters,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5wv73358</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kofman, Rochelle</name>
      </author>
      <author>
        <name>Smartt, Addison</name>
      </author>
      <author>
        <name>Myles, Reginald Jerome</name>
        <uri>https://orcid.org/0009-0001-7731-832X</uri>
      </author>
      <author>
        <name>Kishi, Patrick</name>
      </author>
      <author>
        <name>Rappaport, Douglas</name>
      </author>
      <author>
        <name>Drechsel, Kevin</name>
      </author>
    </item>
    <item>
      <title>Carotid-cavernous Fistula in a Patient with Minimal Head and&amp;nbsp;Facial Trauma: A Case Report</title>
      <link>https://escholarship.org/uc/item/5m21n0nw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Intracranial arterial injury is typically associated with high-energy trauma. &amp;nbsp;Early diagnosis and treatment are essential for improving patients' functional prognosis.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 76-year-old woman complained of pulsatile tinnitus on the 15th day after her traffic accident, in which she got injured only a bruise to her face, while severe injuries to her torso. On the 17th day, ptosis, conjunctival congestion, and an ocular motility disorder developed in her right eye. Magnetic resonance angiography showed a direct high-flow shunt from the internal carotid artery to the cavernous sinus. On the 20th day, the same symptoms developed in her left eye. On the 23rd day, coil embolization to the fistula reduced symptoms in the left eye, but not the right eye.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion: &lt;/strong&gt;This complication rarely occurs in patients with head trauma. Our case indicates that this can occur even in patients...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5m21n0nw</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Miyake, Yoshihiro</name>
      </author>
      <author>
        <name>Abe, Tomohiro</name>
        <uri>https://orcid.org/0000-0001-5585-6381</uri>
      </author>
      <author>
        <name>Kubo, Keisuke</name>
      </author>
      <author>
        <name>Nagoshi, Hideki</name>
      </author>
      <author>
        <name>Ochiai, Hidenobu</name>
      </author>
    </item>
    <item>
      <title>Paradoxical Coronary Embolism as a Cause of Recurrent Myocardial Infarction: A Case Report</title>
      <link>https://escholarship.org/uc/item/51n9m25c</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Paradoxical coronary embolism is a rare cause of myocardial infarction.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 57-year-old man presented with acute chest pain after a recent non-ST elevation&amp;nbsp;myocardial infarction, during which a patent foramen ovale was identified. On readmission, the&amp;nbsp;electrocardiogram showed an inferior ST-elevation myocardial infarction, and angiography revealed&amp;nbsp;a distal thrombotic occlusion in otherwise normal coronary arteries. No venous thromboembolism&amp;nbsp;was found, but thrombophilia testing revealed heterozygous factor V Leiden. He was managed&amp;nbsp;conservatively and underwent successful patent foramen ovale closure.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: This case highlights paradoxical embolism as a diagnostic consideration in acute myocardial infarction without coronary artery disease.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/51n9m25c</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Berckmans, Dago</name>
      </author>
    </item>
    <item>
      <title>Fatal Gastric Perforation Caused by Undiagnosed Trichobezoar in an Adolescent: A Case Report</title>
      <link>https://escholarship.org/uc/item/4z69k3w1</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Trichobezoar is a rare gastrointestinal condition typically caused by ingestion of hair,&amp;nbsp;which most often affects adolescent females. Its clinical presentation is frequently nonspecific, with&amp;nbsp;symptoms such as abdominal pain, constipation, or early satiety, which can delay recognition until&amp;nbsp;severe complications such as obstruction or perforation develop.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We present the case of a 14-year-old girl who developed a massive trichobezoar&amp;nbsp;resulting in gastric perforation and death. She had a three-month history of intermittent constipation&amp;nbsp;and multiple healthcare visits without definitive diagnosis. On arrival to the emergency department,&amp;nbsp;she was in cardiopulmonary arrest. Computed tomography revealed a large intragastric mass&amp;nbsp;with associated pneumoperitoneum. Emergency laparotomy confirmed a trichobezoar with gastric&amp;nbsp;perforation and diffuse peritonitis. Despite prompt surgical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4z69k3w1</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gültekin, Mert</name>
        <uri>https://orcid.org/0009-0001-1285-5490</uri>
      </author>
      <author>
        <name>Erinmez, Ayça</name>
        <uri>https://orcid.org/0009-0003-0653-0053</uri>
      </author>
      <author>
        <name>Karpuz, Yunus Emre</name>
        <uri>https://orcid.org/0009-0008-7163-3784</uri>
      </author>
    </item>
    <item>
      <title>In Reply: Letter to the Editor on “A Case Report of Delayed,&amp;nbsp;Severe, Paroxysmal Muscle Cramping after Chilean Rose&amp;nbsp;Tarantula (Grammostola rosea) Envenomation”</title>
      <link>https://escholarship.org/uc/item/4xm6x30x</link>
      <description>&lt;p&gt;Manuscript: A Case Report of Delayed, Severe, Paroxysmal Muscle Cramping after Chilean Rose Tarantula (Grammostola rosea) Envenomation&amp;nbsp;&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4xm6x30x</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cole, Jon</name>
      </author>
      <author>
        <name>Gooley, Brian Thomas</name>
      </author>
      <author>
        <name>Hughes, Kirk</name>
      </author>
      <author>
        <name>Gooley, Mark</name>
      </author>
      <author>
        <name>Keyler, Daniel</name>
      </author>
      <author>
        <name>Vetter, Richard</name>
      </author>
    </item>
    <item>
      <title>Isolated Radial Collateral Ligament Thumb Tear in a Teenage Cheerleader Base: A Rare Injury from an Overhead Stunt</title>
      <link>https://escholarship.org/uc/item/4ns2d0kx</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Radial collateral ligament injuries of the thumb are rare, especially in adolescent athletes. We present a case of a 17-year-old female cheerleader who sustained a complete radial collateral ligament tear while basing during a cheerleading stunt.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;The patient presented to the emergency department with pain in the right thumb after&amp;nbsp;catching a falling flyer. Examination of the first metacarpophalangeal joint of the right thumb revealed&amp;nbsp;tenderness and laxity. Radiographic imaging showed no fracture. Magnetic resonance imaging&amp;nbsp;confirmed a complete radial collateral ligament tear. She underwent surgical repair with full recovery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: This case highlights an uncommon thumb ligament injury in a non-traditional&amp;nbsp;mechanism. Emergency physicians should consider radial collateral ligament tears in&amp;nbsp;patients with metacarpophalangeal joint tenderness, even when radiographs...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4ns2d0kx</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Baker, Russell Andrew</name>
      </author>
    </item>
    <item>
      <title>Foreign Body-induced Pancreatitis—Multimodal Imaging and&amp;nbsp;Multispecialty Collaboration: A Case Report</title>
      <link>https://escholarship.org/uc/item/4m59j13s</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Foreign body-induced pancreatitis is rare and diagnostically challenging, often&amp;nbsp;presenting with non-specific symptoms and no clear history, unlike typical causes.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 70-year-old man presented with vomiting and abdominal tenderness. Imaging&amp;nbsp;revealed a 4-cm sharp foreign body near the pancreatic head causing inflammation. Endoscopy and&amp;nbsp;endoscopic ultrasound failed to locate the object. Surgical exploration with intraoperative ultrasound&amp;nbsp;identified and removed the foreign body at the pylorus-duodenal junction.&amp;nbsp;The patient recovered&amp;nbsp;without complications.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Early diagnosis, multimodal imaging, and surgical collaboration are essential for optimal&amp;nbsp;management of foreign body-induced pancreatitis.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4m59j13s</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Vaghela, Nital</name>
      </author>
      <author>
        <name>Abou Chaar, Mohamad K.</name>
        <uri>https://orcid.org/0000-0002-9584-2184</uri>
      </author>
      <author>
        <name>Mahnke, Steven</name>
      </author>
      <author>
        <name>Colak, Ceylan</name>
      </author>
      <author>
        <name>Stephens, Daniel</name>
      </author>
      <author>
        <name>Kummer, Tobias</name>
      </author>
    </item>
    <item>
      <title>Bucket Handle Injury in Blunt Abdominal Trauma</title>
      <link>https://escholarship.org/uc/item/4bg1t7pq</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 52-year-old man involved in a high-speed car crash presented with hypotension, abdominal and back pain, and seatbelt bruising. Imaging revealed a mesenteric bucket-handle injury with active bleeding. He received resuscitation and was taken emergently to the&amp;nbsp;operating room for a sigmoid colectomy with primary anastomosis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;In patients with blunt abdominal trauma, 1-6% are diagnosed with mesenteric or&amp;nbsp;hollow visceral injuries; the bucket handle injury is a subtype of these injuries. These injuries often&amp;nbsp;present subtly and may be missed on initial evaluation, particularly when the extended focused&amp;nbsp;assessment with sonography for trauma is negative. Unexplained hemodynamic instability should&amp;nbsp;prompt further investigation, as delayed diagnosis can lead to bowel ischemia or infarction. Early&amp;nbsp;recognition and surgical intervention are critical to reducing morbidity and mortality...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4bg1t7pq</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gottam, Bhargavesh</name>
      </author>
      <author>
        <name>McCoy, Christopher Eric</name>
      </author>
    </item>
    <item>
      <title>Atypical Presentation of Metformin-Associated Lactic Acidosis: A Case Report</title>
      <link>https://escholarship.org/uc/item/3wk9474r</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Metformin, a first-line type two diabetes medication, is generally considered safe and&amp;nbsp;effective. However, it is rarely associated with life-threatening lactic acidosis. This generally presents&amp;nbsp;in patients with gastrointestinal upset as a primary complaint. It is most common in patients with&amp;nbsp;underlying chronic kidney disease. Prevention of associated mortality requires early diagnosis and&amp;nbsp;intervention with fluids, bicarbonate, vasopressors, and hemodialysis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;This is a notable presentation of metformin toxicity, as the 68-year-old male patient&amp;nbsp;presented with an atypical chief complaint of dyspnea and no history of kidney disease. Physical exam&amp;nbsp;was notable for tachypnea and clear breath sounds. Labs revealed anion gap metabolic acidosis from&amp;nbsp;an accumulation of lactic acid and acute renal failure. Other causes of lactic acid metabolic acidosis&amp;nbsp;were considered and ruled out....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3wk9474r</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Welsch, Elizabeth</name>
        <uri>https://orcid.org/0009-0005-3237-6111</uri>
      </author>
      <author>
        <name>Evans, Jerome</name>
        <uri>https://orcid.org/0009-0006-7610-3809</uri>
      </author>
      <author>
        <name>Yoxall, Alexander</name>
        <uri>https://orcid.org/0009-0004-5625-3311</uri>
      </author>
      <author>
        <name>Culhane, Anna</name>
        <uri>https://orcid.org/0009-0006-5032-868X</uri>
      </author>
    </item>
    <item>
      <title>Unexpected Cardiac Asystole Caused by Vasovagal Reaction&amp;nbsp;During Venipuncture: A Case Report</title>
      <link>https://escholarship.org/uc/item/3t05q7rj</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: The vasovagal reaction can lead to benign, self-limiting syncope triggered by stimuli&amp;nbsp;such as pain or emotional stress. However, in rare and severe cases it may result in cardiac&amp;nbsp;asystole. Previous episodes of vasovagal reactions could be a risk factor for cardiac asystole.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We present a 39-year-old male with a previous episode of vasovagal syncope who&amp;nbsp;developed an unexpected 15-second episode of asystole during venipuncture, for which we performed&amp;nbsp;immediate chest compressions. Further evaluations revealed no apparent underlying cause. The&amp;nbsp;patient was subsequently diagnosed with transient asystole secondary to vasovagal reaction.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: While venipuncture is a common procedure in clinical practice, clinicians should be&amp;nbsp;aware of the potential risk for cardiac asystole. Detailed medical history of previous episodes of&amp;nbsp;vasovagal reactions could be...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3t05q7rj</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Nagano, Tomoki</name>
        <uri>https://orcid.org/0009-0009-8455-5938</uri>
      </author>
      <author>
        <name>Sakuma, Ryo</name>
      </author>
      <author>
        <name>Horiguchi, Wataru</name>
      </author>
      <author>
        <name>Jeong, Soi</name>
      </author>
      <author>
        <name>Tanamoto, Takaki</name>
      </author>
      <author>
        <name>Yokota, Yumi</name>
      </author>
      <author>
        <name>Fowler, Matthew</name>
      </author>
      <author>
        <name>Kim, Jin</name>
      </author>
    </item>
    <item>
      <title>A Case of Ureter Herniation in the Petit Triangle</title>
      <link>https://escholarship.org/uc/item/3h40g6jv</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;An 88-year-old man was brought to our emergency department due to altered&amp;nbsp;mental status and hemodynamic shock due to a urinary tract infection. Computed tomography&amp;nbsp;showed an incarcerated ureter in the Petit triangle. Urology was consulted, and the hernia was&amp;nbsp;reduced back into the retroperitoneal cavity.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;Petit hernia is rare; moreover, there is no literature to our knowledge discussing the&amp;nbsp;ureter as the herniated structure. Interventional radiology can be considered as a reductive option.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3h40g6jv</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tanaka, Atsuhito</name>
      </author>
      <author>
        <name>Kamitani, Yuka</name>
      </author>
    </item>
    <item>
      <title>Catching Silent Heart Killers—How Bedside Ultrasound&amp;nbsp;Revealed Hidden Endocarditis: A Case Report</title>
      <link>https://escholarship.org/uc/item/3g07934h</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;In this report we highlight the emerging role of pediatric cardiac point-of-care&amp;nbsp;ultrasound (POCUS) in rapidly diagnosing infective endocarditis, using a clinical case as illustration.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;:&amp;nbsp;A six-year-old girl with a known ventricular septal defect presented with worsening&amp;nbsp;respiratory symptoms, fevers, abdominal pain, and decreased oral intake. Initial POCUS, performed&amp;nbsp;by an emergency physician, indicated a suspicious echogenic mass in the right atrium, prompting&amp;nbsp;formal echocardiography. Further imaging and cultures confirmed infective endocarditis due to&amp;nbsp;methicillin-sensitive&amp;nbsp;&lt;em&gt;Staphylococcus aureus&lt;/em&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: This case underscores the utility of pediatric cardiac POCUS as a rapid bedside&amp;nbsp;diagnostic tool for infective endocarditis in emergency settings, leading to early diagnosis and&amp;nbsp;management. Although POCUS cannot replace comprehensive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3g07934h</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dhillon, Reshvinder</name>
      </author>
      <author>
        <name>Mcmullin, Sarah</name>
      </author>
    </item>
    <item>
      <title>Rare Case of Ethmoidal Encephalocele and Sequelae</title>
      <link>https://escholarship.org/uc/item/2cd7n7dd</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 64-year-old Black female presented to the emergency department following a new-onset tonic-clonic seizure. The patient had been given 2 milligrams of lorazepam by emergency medical services with cessation of seizure activity. On physical exam she was lethargic and had&amp;nbsp;clear discharge from the right nare. Computed tomography of the brain initially demonstrated&amp;nbsp;findings consistent with sinusitis versus ethmoidal mass. Magnetic resonance imaging of the brain&amp;nbsp;demonstrated a right frontal ethmoidal encephalocele.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;Basal encephaloceles occur due to a defect in the skull base. Location of the defect&amp;nbsp;and extracranial herniation of brain tissue can cause neurologic sequelae. This case illustrates the&amp;nbsp;importance of maintaining a broad differential diagnosis and for emergency physicians to obtain&amp;nbsp;imaging when evaluating seizures and/or chronic rhinorrhea in adults.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cd7n7dd</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Kiveum</name>
      </author>
      <author>
        <name>Craig, Taylor</name>
      </author>
      <author>
        <name>Delicio, Lucas</name>
      </author>
      <author>
        <name>Scumpia, Alexander John</name>
        <uri>https://orcid.org/0000-0001-6862-6315</uri>
      </author>
    </item>
    <item>
      <title>Letter to the Editor: A Case Report of Delayed, Severe, Paroxysmal Muscle&amp;nbsp;Cramping After Chilean Rose Tarantula (&lt;em&gt;Grammostola rosea&lt;/em&gt;)&amp;nbsp;Envenomation</title>
      <link>https://escholarship.org/uc/item/2c36p0r0</link>
      <description>Letter to the Editor: A Case Report of Delayed, Severe, Paroxysmal Muscle&amp;nbsp;Cramping After Chilean Rose Tarantula (&lt;em&gt;Grammostola rosea&lt;/em&gt;)&amp;nbsp;Envenomation</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2c36p0r0</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Roque, Luis A</name>
        <uri>https://orcid.org/0000-0003-1969-0315</uri>
      </author>
    </item>
    <item>
      <title>Preoperative Diagnosis of Amyand Hernia in the Emergency&amp;nbsp;Department with Point-of-care Ultrasound: A Case Report</title>
      <link>https://escholarship.org/uc/item/1qn446rw</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Amyand hernia is a rare condition in which the appendix is found within an inguinal hernia&amp;nbsp;sac, often mimicking incarcerated or strangulated hernias. Diagnosis is typically made intraoperatively,&amp;nbsp;but increasing use of point-of-care ultrasound (POCUS) is enhancing preoperative recognition.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 46-year-old male presented with a chronic, partially reducible inguinal hernia. Point-of-care ultrasound revealed a bowel-containing hernia with fluid. Computed tomography confirmed&amp;nbsp;an inflamed appendix within the sac. Laparoscopic appendectomy and open hernia repair were&amp;nbsp;performed without complications.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1qn446rw</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wallace, Neil</name>
      </author>
      <author>
        <name>Hauger, Aila Suga</name>
      </author>
    </item>
    <item>
      <title>Methicillin Resistant&lt;em&gt; Staphylococcus Aureus&lt;/em&gt; Septic Internal Jugular Thrombophlebitis: A Case Report</title>
      <link>https://escholarship.org/uc/item/1k44h5x9</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Lemierre syndrome is characterized by septic thrombophlebitis of the internal jugular&amp;nbsp;vein, classically caused by&amp;nbsp;&lt;em&gt;Fusobacterium necrophorum&lt;/em&gt;. It is typically seen after an episode of&amp;nbsp;pharyngitis where the palatine tonsils or peritonsillar mucosa is affected. It is thought to spread&amp;nbsp;locally into the pharyngeal space toward the internal jugular vein.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 42-year-old male with progressively worsening, atraumatic right-sided neck pain&amp;nbsp;was discovered to have methicillin-resistant &lt;em&gt;Staphylococcus aureus &lt;/em&gt;(MRSA) bacteremia, septic thrombophlebitis of the right dural venous sinuses, skull base osteomyelitis, and otomastoiditis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;While septic thrombophlebitis of the dural venous sinuses and internal jugular&amp;nbsp;vein is typically caused by &lt;em&gt;F necrophorum &lt;/em&gt;and usually comes from local pharyngeal spread,&amp;nbsp;community-acquired MRSA is...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1k44h5x9</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kowalczyk, Daniel</name>
      </author>
      <author>
        <name>Ubiñas, George</name>
      </author>
    </item>
    <item>
      <title>Hemothorax from a Thoracic Chalk-Stick Fracture in Ankylosing Spondylitis: A Case Report</title>
      <link>https://escholarship.org/uc/item/1gc895jz</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Chalk-stick fractures are transverse spinal injuries seen in patients with ankylosing&amp;nbsp;spondylitis due to chronic inflammation and spinal rigidity. These fractures may result from minor&amp;nbsp;trauma and are associated with potentially fatal complications. While spinal fractures in ankylosing&amp;nbsp;spondylitis are well recognized, thoracic chalk-stick fractures complicated by hemothorax from&amp;nbsp;vascular injury remain exceedingly rare. We present a case of an elderly male with ankylosing&amp;nbsp;spondylitis who sustained a thoracic chalk-stick fracture following a ground-level fall, complicated&amp;nbsp;by hemothorax and hemorrhagic shock. This case highlights a rarely reported but life-threatening&amp;nbsp;complication and emphasizes the importance of early imaging and high clinical suspicion in this high-risk population—even after minor trauma.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 90-year-old male with known history of ankylosing spondylitis presented...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1gc895jz</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dehkordi, Armin Akbarpur</name>
        <uri>https://orcid.org/0000-0002-3492-4194</uri>
      </author>
      <author>
        <name>Aloise, Daniel Michael</name>
      </author>
      <author>
        <name>Scheppke, Eric</name>
      </author>
      <author>
        <name>Christodoulou, Mary</name>
      </author>
      <author>
        <name>Gigliotti, Grayson</name>
      </author>
      <author>
        <name>Zitek, Tony</name>
        <uri>https://orcid.org/0000-0002-4357-6611</uri>
      </author>
    </item>
    <item>
      <title>Myocardial Crypts on Ultrasound in a Young Female with Exertional Syncope</title>
      <link>https://escholarship.org/uc/item/1fp5v5fw</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A 20-year-old female with no past medical history presented to the emergency&amp;nbsp;department (ED) after an episode of exertional syncope. Physical examination, vital signs, and&amp;nbsp;electrocardiogram were unremarkable. Point-of-care ultrasound revealed abnormal invaginations&amp;nbsp;in the interventricular septum. Laboratory evaluation was significant for markedly elevated troponin&amp;nbsp;concerning for cardiac arrest. She was admitted to cardiology with suspicion for genetic cardiomyopathy.&amp;nbsp;The patient underwent placement of an implantable cardioverter defibrillator after cardiac magnetic&amp;nbsp;resonance imaging redemonstrated the septal invaginations known as myocardial crypts. Genetic&amp;nbsp;studies later revealed sarcomere gene mutations associated with hypertrophic cardiomyopathy.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;Myocardial crypts, which are invaginations within the myocardium, are considered&amp;nbsp;early morphological markers for...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1fp5v5fw</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Allen, Christopher Wei</name>
      </author>
      <author>
        <name>Gubbels, Alexandra</name>
      </author>
      <author>
        <name>Duanmu, Youyou</name>
      </author>
      <author>
        <name>Vogel, Jody</name>
      </author>
    </item>
    <item>
      <title>53-year-old Woman with Opsoclonus-Myoclonus Syndrome</title>
      <link>https://escholarship.org/uc/item/1f65799z</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;We present the case of a 53-year-old female with darting eye movements and difficulty walking who was found to have opsoclonus-myoclonus syndrome only after multiple&amp;nbsp;presentations to emergency departments over five days.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;Adult-onset opsoclonus-myoclonus syndrome is a rare central nervous system&amp;nbsp;disease typically associated with paraneoplastic or idiopathic etiologies. With non-specific symptom&amp;nbsp;presentation, this condition is commonly misdiagnosed in adults, leading to diagnostic delays and&amp;nbsp;long-term motor and cognitive sequelae.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1f65799z</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Stephens, Taylor O</name>
      </author>
      <author>
        <name>Imhoff, Bryan</name>
      </author>
      <author>
        <name>Patel, Janak</name>
      </author>
    </item>
    <item>
      <title>The Value of Point-of-care Ocular Ultrasound in Physician-in-triage Model: A Case Series</title>
      <link>https://escholarship.org/uc/item/1c1110m0</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Physician-in-triage (PIT) models have become increasingly common in emergency&amp;nbsp;medicine. The goal is to facilitate rapid patient evaluation and improve key operational emergency&amp;nbsp;department (ED) metrics. However, there is limited time for the PIT encounter, which often involves&amp;nbsp;an abbreviated patient evaluation. Point-of-care ultrasound (POCUS) has been shown to improve&amp;nbsp;patient care and speed diagnosis in a variety of scenarios. Although physicians working within a PIT&amp;nbsp;model must remain mindful of time constraints, POCUS can help identify time-sensitive diagnoses&amp;nbsp;and guide appropriate initial testing during certain encounters. Ocular POCUS can be particularly&amp;nbsp;impactful on timely diagnosis and appropriate deployment of ED resources.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series: &lt;/strong&gt;We present three cases of acute monocular vision loss wherein the PIT physician&amp;nbsp;used ocular POCUS to arrive at the correct initial diagnosis....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1c1110m0</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Thom, Christopher</name>
        <uri>https://orcid.org/0000-0003-1435-2712</uri>
      </author>
      <author>
        <name>Spirek, Benton</name>
      </author>
      <author>
        <name>Bhargava, Gitansh</name>
      </author>
      <author>
        <name>Moak, James</name>
      </author>
    </item>
    <item>
      <title>Neurotoxic Snakebite Presenting with Early Neck Pain and&amp;nbsp;Muscle Weakness: A Case Report of a Diagnostic Pitfall</title>
      <link>https://escholarship.org/uc/item/1b33b9mh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Neurotoxic envenomation often presents with non-specific neurological symptoms and&amp;nbsp;minimal local signs, which can delay appropriate diagnosis and treatment.&amp;nbsp;This is the first reported&amp;nbsp;case of a neurotoxic snakebite presenting with an atypical symptom of unilateral neck pain.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 12-year-old girl was referred to our emergency centre with neck weakness&amp;nbsp;progressing to quadriplegia, attributed to a fall while playing.&amp;nbsp;A diagnosis of acute flaccid paralysis&amp;nbsp;secondary to cervical trauma was made and treated at the first hospital; however, she developed&amp;nbsp;respiratory distress and was transferred to our centre. Clinical examination and computed&amp;nbsp;tomography ruled out cervical cord injury. A diagnosis of neurotoxic envenomation was considered,&amp;nbsp;given our centre’s high snakebite burden and the symptom of descending flaccid paralysis. Despite&amp;nbsp;initiating antivenom and supportive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1b33b9mh</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>T, Neithiya</name>
      </author>
      <author>
        <name>Nair, Jayan Jayapalan</name>
      </author>
      <author>
        <name>Chavali, Krishna Dutt</name>
      </author>
    </item>
    <item>
      <title>Clinical Practice and Cases in Emergency Medicine Volume 10 Issue 2</title>
      <link>https://escholarship.org/uc/item/1607g892</link>
      <description>&lt;p&gt;n/a&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1607g892</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>CPC-EM, Clinical Practice and Cases in Emergency Medicine</name>
      </author>
    </item>
    <item>
      <title>More than Just a Bag—Purple Urine Bag Syndrome as a&amp;nbsp;Manifestation of Vulnerability in Geriatric Patients:&amp;nbsp;A Case Report</title>
      <link>https://escholarship.org/uc/item/0x38b68m</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Purple urine bag syndrome (PUBS) is an uncommon yet visually striking condition&amp;nbsp;observed in patients with long-term urinary catheters. It is associated with urinary tract infections&amp;nbsp;caused by bacteria that metabolize tryptophan into indigo and indirubin pigments. Although typically&amp;nbsp;benign, PUBS can signal underlying medical and social vulnerability.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We describe a 78-year-old woman with multiple sclerosis and chronic suprapubic&amp;nbsp;catheterization who presented with failure to thrive and concerns for caregiver fatigue. A striking&amp;nbsp;finding on arrival was the deep purple discoloration of her urine in the Foley bag, consistent&amp;nbsp;with PUBS. Additionally, she was tachycardic and had extensive, unstageable pressure ulcers.&amp;nbsp;Laboratory studies revealed leukocytosis, lactic acidosis, and acute kidney injury. Imaging&lt;br&gt;suggested sacral osteomyelitis, stercoral colitis, and aspiration...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0x38b68m</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>White, Lindsey McKissick</name>
        <uri>https://orcid.org/0009-0007-8428-8759</uri>
      </author>
      <author>
        <name>Rivera, Megan</name>
        <uri>https://orcid.org/0009-0004-3157-2690</uri>
      </author>
      <author>
        <name>Nash, Christopher James</name>
        <uri>https://orcid.org/0000-0002-0738-409X</uri>
      </author>
      <author>
        <name>Natesan, Sreeja</name>
      </author>
    </item>
    <item>
      <title>The Complexity of Weak Rhesus Positivity in Pregnancy: Challenges and Management</title>
      <link>https://escholarship.org/uc/item/0vn2b019</link>
      <description>The Complexity of Weak Rhesus Positivity in Pregnancy: Challenges and Management</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0vn2b019</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Luksanapisitakul, Vimoltip</name>
      </author>
      <author>
        <name>Alojayli, Anas</name>
        <uri>https://orcid.org/0000-0001-7817-3399</uri>
      </author>
    </item>
    <item>
      <title>Myocardial Infarction in a 19-year-old with a History of Kawasaki Disease: A Case Report</title>
      <link>https://escholarship.org/uc/item/0g2110tf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Kawasaki disease is a vasculitis most commonly affecting children under five years of&amp;nbsp;age but can also occur in older children and adults. When not sufficiently treated, Kawasaki disease&amp;nbsp;can lead to cardiac complications such as myocarditis and coronary artery aneurysms, with aneurysms&amp;nbsp;being the most serious long-term complication as it poses a risk for acute coronary syndrome.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 19-year-old with remote history of Kawasaki disease presented to the emergency&amp;nbsp;department with chest pain, diaphoresis, and emesis after being struck in the chest by another&amp;nbsp;player during a basketball game. Despite his young age and reported mild musculoskeletal trauma,&amp;nbsp;an electrocardiogram and troponin were ordered. Electrocardiogram findings were concerning for&amp;nbsp;ischemia, and troponin was elevated, confirming myocardial infarction and prompting a cardiology&amp;nbsp;consult. Urgent percutaneous...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0g2110tf</guid>
      <pubDate>Fri, 24 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sethman, Chad</name>
        <uri>https://orcid.org/0009-0001-7525-342X</uri>
      </author>
      <author>
        <name>Sethman, Jessica</name>
      </author>
      <author>
        <name>End, Bradley</name>
      </author>
    </item>
    <item>
      <title>CPC-EM Full-Text Issue Volume 10 Issue 1</title>
      <link>https://escholarship.org/uc/item/8tz1c8wf</link>
      <description>&lt;p&gt;n/a&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8tz1c8wf</guid>
      <pubDate>Tue, 3 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>CPC-EM, Clinical Practice and Cases in Emergency Medicine</name>
      </author>
    </item>
    <item>
      <title>Pleural and Pericardial Effusions Associated with Semaglutide:&amp;nbsp;A Case Report</title>
      <link>https://escholarship.org/uc/item/2nq2949g</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Semaglutide, a glucagon-like peptide-1 receptor&amp;nbsp;agonist, has gained increasing&amp;nbsp;popularity for managing both type 2 diabetes mellitus and obesity. However, as its use increases,&amp;nbsp;new adverse events are emerging. This case report presents a 70-year-old patient who developed&amp;nbsp;pleural and pericardial effusions likely related to semaglutide use.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: Four weeks after being prescribed semaglutide, a 70-year-old woman presented to&amp;nbsp;the emergency department (ED) with shortness of breath. Diagnostic testing in the ED and hospital&amp;nbsp;revealed that she had both pericardial and exudative pleural effusions, along with a positive anti-nuclear antibody and elevated inflammatory markers. Her signs and symptoms improved with steroid&amp;nbsp;administration, and no other etiology was identified.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;The patient was diagnosed with drug-induced lupus, likely triggered by...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2nq2949g</guid>
      <pubDate>Thu, 22 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Stark, Maggie</name>
      </author>
      <author>
        <name>Valentini, Nicholas</name>
      </author>
    </item>
    <item>
      <title>Recurrent Miller Fisher Syndrome: A Case Report</title>
      <link>https://escholarship.org/uc/item/6g61255f</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Guillain-Barré syndrome (GBS) can manifest with progressive paralysis, requiring careful monitoring and treatment with steroids or IVIG. While this disease can be devastating and require ICU level of care, there are few incidences of GBS relapses.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report:&amp;nbsp; &lt;/strong&gt;A 67-year-old man with a past medical history of Miller Fisher Syndrome (MFS) variant Guillain-Barre Syndrome (GBS), with complete recovery presenting to the emergency department (ED) with ataxia, ophthalmoplegia, dysphonia, and ambulatory dysfunction. The patient noticed his neurologic symptoms after waking up and presented to the ED with physical examination positive for difficulty with upward gaze, mild right lower facial droop, dysmetria with left finger to nose testing, and unsteady gait. &amp;nbsp;A lumbar puncture (LP) revealed albuminocytologic dissociation and he was diagnosed with recurrent MFS. The patient completed a five-day course of intravenous...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g61255f</guid>
      <pubDate>Tue, 20 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Vernier, Larry</name>
      </author>
      <author>
        <name>Barnes Gilmore, Griffin</name>
      </author>
      <author>
        <name>Van Housen, Kelsey</name>
        <uri>https://orcid.org/0009-0008-3906-4438</uri>
      </author>
      <author>
        <name>Zhang, Xiao Chi</name>
      </author>
    </item>
    <item>
      <title>Carotidynia—A Rare Cause of Anterior Neck Pain:&amp;nbsp;Case Report</title>
      <link>https://escholarship.org/uc/item/2cp8v219</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Carotidynia is a rare, often under-diagnosed condition characterized by idiopathic&amp;nbsp;inflammation around the carotid artery, presenting with unilateral neck pain that typically resolves&amp;nbsp;within two weeks.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 32-year-old male presented with intermittent right anterior neck pain for two&amp;nbsp;years, with no other associated symptoms. Computed tomography revealed carotid perivascular&amp;nbsp;inflammation, consistent with carotidynia.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;Although self-limited, carotidynia should be considered in patients with unexplained&amp;nbsp;neck pain, as its recognition is crucial to differentiate it from more serious conditions and to avoid&amp;nbsp;mismanagement or unnecessary interventions.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cp8v219</guid>
      <pubDate>Tue, 20 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ibu, Faith</name>
        <uri>https://orcid.org/0000-0003-1950-0809</uri>
      </author>
      <author>
        <name>Keller-Baruch, Olivia</name>
      </author>
      <author>
        <name>Pelletier, Jessica</name>
        <uri>https://orcid.org/0000-0003-1494-6764</uri>
      </author>
    </item>
    <item>
      <title>When STEMI Isn’t STEMI: Cardiac Arrest from Aortic Valve Papillary Fibroelastoma – A Case Report</title>
      <link>https://escholarship.org/uc/item/0px540gp</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Cardiac arrest remains a major global cause of mortality, with both structural and&amp;nbsp;non-structural cardiac abnormalities implicated. While ischemic heart disease is a common etiology,&amp;nbsp;rare conditions such as papillary fibroelastoma can also result in life-threatening events through&amp;nbsp;embolization or coronary obstruction. Timely recognition and advanced cardiac imaging, particularly&amp;nbsp;transesophageal echocardiography, are essential in such atypical presentations.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 61-year-old female with a history of ischemic heart disease presented to the&amp;nbsp;emergency department following an out-of-hospital cardiac arrest. Initial electrocardiogram (ECG)&amp;nbsp;demonstrated anterior ST-elevation myocardial infarction, which resolved on repeat ECG, prompting&amp;nbsp;reconsideration of the underlying cause. The patient achieved return of spontaneous circulation&amp;nbsp;twice and eventually self-extubated. Further investigation,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0px540gp</guid>
      <pubDate>Fri, 16 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kanaa, Mohammad Wasim Mohammad Zouhir</name>
        <uri>https://orcid.org/0009-0003-8643-8344</uri>
      </author>
      <author>
        <name>Abbastanira, Shahd H I</name>
        <uri>https://orcid.org/0009-0009-1174-5124</uri>
      </author>
      <author>
        <name>Elameen, Essra Mohamed Abdullah</name>
        <uri>https://orcid.org/0000-0003-3687-8627</uri>
      </author>
      <author>
        <name>Alsultan, Sarah Emad</name>
        <uri>https://orcid.org/0009-0005-9243-8310</uri>
      </author>
    </item>
    <item>
      <title>Antimuscarinic Toxicity Safely Managed with High-Dose&amp;nbsp;Transdermal Rivastigmine: A Case Report</title>
      <link>https://escholarship.org/uc/item/0f10d1kc</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Antimuscarinic toxicity, which can cause delirium and unsafe behavior, may result&amp;nbsp;from an adverse effect of prescribed medications or from non-medical substance use. Physostigmine&amp;nbsp;shortages have prompted use of transdermal rivastigmine for management of antimuscarinic toxicity;&amp;nbsp;however, symptom control is equivocal at standard dosing.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A patient with antimuscarinic toxicity was treated with physostigmine and transitioned to&amp;nbsp;26.6 milligrams/24 hours transdermal rivastigmine for sustained symptom control. He experienced no&amp;nbsp;adverse effects and tolerated floor admission.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;There is mechanistic plausibility supporting safe, sustained control of antimuscarinic&amp;nbsp;toxicity with high-dose transdermal rivastigmine. Central distribution is more rapid than serum&amp;nbsp;distribution and higher doses correlate with a shorter time to peak concentration.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0f10d1kc</guid>
      <pubDate>Fri, 16 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Watson, Christopher James</name>
        <uri>https://orcid.org/0000-0002-1003-5798</uri>
      </author>
      <author>
        <name>Burrill, Emilie M.</name>
      </author>
      <author>
        <name>Jaffee, William S.</name>
      </author>
    </item>
    <item>
      <title>Spontaneous Splenic Vein Rupture: Case Report of a&amp;nbsp;Rare Presentation</title>
      <link>https://escholarship.org/uc/item/9fh5w06s</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Spontaneous splenic vein rupture is a rare condition associated with a high risk of&amp;nbsp;mortality. Only a few cases have been documented, all of which have been linked to underlying&amp;nbsp;predisposing conditions. In this case, however, we present a previously healthy patient with no&amp;nbsp;identifiable risk factors.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 64-year-old male presented to the emergency department with acute-onset&amp;nbsp;abdominal pain and nausea. Physical exam revealed a rigid abdomen with diffuse tenderness and&amp;nbsp;guarding. Serial labs revealed a progressively decreasing hemoglobin and red blood cell count.&amp;nbsp;Computed tomography demonstrated a ruptured splenic vein with a large volume of retroperitoneal&amp;nbsp;hemorrhage. Laparotomy identified a large retroperitoneal hematoma with hemoperitoneum, and&amp;nbsp;embolization was performed by interventional radiology. The patient recovered after one week in the&amp;nbsp;surgical intensive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9fh5w06s</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Franco, Brittany</name>
      </author>
      <author>
        <name>Karski, Amanda</name>
      </author>
      <author>
        <name>Boehm, Kevin</name>
      </author>
    </item>
    <item>
      <title>Medial Clavicle Physeal Fracture in a 15-Year-Old Male: A Case Report</title>
      <link>https://escholarship.org/uc/item/7ph799nh</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Sternoclavicular joint injuries are rare and potentially life-threatening injuries&amp;nbsp;due to their proximity to vital mediastinal structures. In adolescents, skeletal immaturity can&amp;nbsp;add complexity to the injury due to potential involvement of the physis. A physeal fracture with&amp;nbsp;displacement can appear as a dislocation on imaging, also known as pseudo-dislocation.&amp;nbsp;Additionally, this anatomic area is difficult to visualize with plain radiographs, which can result in&amp;nbsp;misdiagnosis and delayed treatment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We present a case of a 15-year-old male athlete who presented to the emergency&amp;nbsp;department with severe right clavicular pain four hours after sustaining a football injury. Plain&amp;nbsp;radiographs obtained at an outside facility as well as repeat plain radiographs at our facility showed&amp;nbsp;no evidence of fracture or dislocation. The patient’s degree of pain and physical exam findings&amp;nbsp;prompted...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7ph799nh</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kofman, Rochelle</name>
      </author>
      <author>
        <name>Allen, Ryan</name>
      </author>
      <author>
        <name>Smartt, Addison B</name>
        <uri>https://orcid.org/0009-0007-3161-9358</uri>
      </author>
      <author>
        <name>Drechsel, Kevin</name>
      </author>
      <author>
        <name>Pollock, Jordan Riley</name>
      </author>
      <author>
        <name>Rappaport, Douglas</name>
      </author>
    </item>
    <item>
      <title>Syncope in a Patient with Takotsubo Syndrome:&amp;nbsp;Additional Issues to Consider</title>
      <link>https://escholarship.org/uc/item/6fz4w39f</link>
      <description>Syncope in a Patient with Takotsubo Syndrome:&amp;nbsp;Additional Issues to Consider</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6fz4w39f</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Madias, John E.</name>
      </author>
    </item>
    <item>
      <title>Syncope in a Patient with Right Ventricular Compression from Severe Pectus Excavatum: A Case Report</title>
      <link>https://escholarship.org/uc/item/3w71h2v8</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Pectus excavatum (PEX) is the most common congenital chest wall deformity,&amp;nbsp;characterized by posterior depression of the sternum and lower costal margin. While often&amp;nbsp;asymptomatic, severe PEX can lead to compression of the heart and great vessels, potentially&amp;nbsp;causing right ventricular dysfunction, syncope, and other cardiovascular symptoms. Syncope due to&amp;nbsp;right ventricle compression in PEX is rare but can significantly impact quality of life and may require&amp;nbsp;surgical intervention.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;:&amp;nbsp;An 18-year-old female presented to the emergency department after an unwitnessed&amp;nbsp;syncopal episode. The patient reported feeling lightheaded while showering, followed by collapse and&amp;nbsp;brief loss of consciousness. Diagnostic testing revealed normal neurological and metabolic parameters&amp;nbsp;including point-of-care glucose, electrocardiogram, serum troponin, electrolytes, and head computed&amp;nbsp;tomography....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3w71h2v8</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Christensen, Matthew John</name>
        <uri>https://orcid.org/0009-0006-1224-1399</uri>
      </author>
      <author>
        <name>Foti, Jennifer</name>
      </author>
    </item>
    <item>
      <title>A Case Report of Acute Lymphoblastic Leukemia Presenting as Bilateral Knee Pain in a Healthy Runner</title>
      <link>https://escholarship.org/uc/item/7jx7d00h</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Acute lymphoblastic leukemia (ALL) is typically a childhood disease but may present&amp;nbsp;in older patients in rare occurrences. Due to its significant morbidity and mortality, early diagnosis&amp;nbsp;is crucial. The symptoms of ALL may be non-specific, making the initial diagnosis difficult leading to&amp;nbsp;delayed treatment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We present the case of a 34-year-old, healthy male runner presenting to the&amp;nbsp;emergency department with a common complaint of bilateral knee pain, who was ultimately&amp;nbsp;diagnosed with ALL with signs of tumor lysis syndrome leading to premature death.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;We discuss the presenting symptoms of acute lymphoblastic leukemia, which may&amp;nbsp;include joint or knee pain as well as leukemic arthritis. We further discuss the importance of&amp;nbsp;clinicians maintaining a high level of suspicion for the “bounce-back” patient and avoiding taking&amp;nbsp;cognitive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7jx7d00h</guid>
      <pubDate>Mon, 5 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Rosselli, Michael</name>
      </author>
      <author>
        <name>Sanoja, Alejandro Jesus</name>
      </author>
      <author>
        <name>Apicella, Matthew</name>
      </author>
    </item>
    <item>
      <title>Acute Aortic Dissection Masquerading as Testicular Torsion:&amp;nbsp;A Case Report</title>
      <link>https://escholarship.org/uc/item/12q6f8hs</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Aortic dissection is a rare but life-threatening condition with a high mortality rate if&amp;nbsp;diagnosis is delayed. Aortic dissection classically presents with sudden-onset, sharp pain in the chest&amp;nbsp;or back. However, atypical presentations can also occur, which could lead to a delay in diagnosis.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A patient initially presented to the emergency department (ED) with left testicular pain&amp;nbsp;ongoing for several hours. On examination, he had tenderness in the left lower quadrant abdomen&amp;nbsp;and left testicle. A testicular ultrasound revealed decreased blood flow to the left testicle, raising&amp;nbsp;concern for testicular torsion. The patient was taken to the operating room, where no torsion was&amp;nbsp;found, and he was subsequently discharged home. Several days later, the patient returned to the ED&amp;nbsp;with worsening pain radiating to the back. A computed tomography revealed an acute type A aortic&amp;nbsp;dissection...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/12q6f8hs</guid>
      <pubDate>Mon, 5 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lo, Bruce M</name>
        <uri>https://orcid.org/0000-0001-6210-9667</uri>
      </author>
      <author>
        <name>Christensen, Megyn K</name>
      </author>
      <author>
        <name>Byrns, Coral E</name>
      </author>
      <author>
        <name>Chidester, Benjamin</name>
      </author>
    </item>
    <item>
      <title>Diagnosis of Bilateral Quadriceps Tendon Rupture using Point-of-Care Ultrasound</title>
      <link>https://escholarship.org/uc/item/10r9605c</link>
      <description>&lt;p&gt;&lt;strong&gt;Case Presentation: &lt;/strong&gt;A healthy 32-year-old man presented to the emergency department with&amp;nbsp;bilateral knee pain after landing from a jump. He was unable to extend his knees and had pain to&amp;nbsp;palpation superior to the patella. Bilateral quadriceps tendon rupture was confirmed using point-of-care ultrasound, and the patient underwent operative repair the next day.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Discussion&lt;/strong&gt;:&amp;nbsp;Bilateral quadriceps tendon rupture is exceedingly rare, which often leads to&amp;nbsp;misdiagnosis. Magnetic resonance imaging is the gold standard diagnostic imaging study but has&amp;nbsp;multiple disadvantages, especially in emergency settings. Point-of-care ultrasound is an excellent&amp;nbsp;tool to screen for this injury and prevent morbidity from delay in surgical repair.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/10r9605c</guid>
      <pubDate>Mon, 5 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Guo, Edward</name>
      </author>
      <author>
        <name>Duran, Akaysha</name>
      </author>
      <author>
        <name>Kuc, Alexander</name>
      </author>
      <author>
        <name>Cheng, Alfred</name>
      </author>
    </item>
    <item>
      <title>A Case Report of Milk-Alkali Syndrome Secondary to&amp;nbsp;Excessive Antacid Use</title>
      <link>https://escholarship.org/uc/item/6wj9x771</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Milk-alkali syndrome is characterized by the triad of hypercalcemia, metabolic&amp;nbsp;alkalosis, and acute kidney injury resulting from excessive intake of calcium and absorbable alkali.&amp;nbsp;Despite falling out of prominence with the advent of modern ulcer treatments, milk-alkali syndrome&amp;nbsp;has experienced a resurgence with the widespread availability of over-the-counter calcium&amp;nbsp;preparations,&amp;nbsp;which now account for up to 10% of hypercalcemia cases.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 60-year-old man with multiple comorbidities presented to the emergency department with altered mental status after his scheduled kyphoplasty was canceled due to concerning neurological findings. Laboratory evaluation revealed severe hypercalcemia, marked metabolic alkalosis, and acute kidney injury. Further history revealed excessive antacid consumption for heartburn. The patient was diagnosed with milk-alkali syndrome, treated with intravenous...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6wj9x771</guid>
      <pubDate>Thu, 1 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Abubshait, Layla</name>
        <uri>https://orcid.org/0000-0002-5577-7074</uri>
      </author>
      <author>
        <name>Beso, Samir</name>
      </author>
    </item>
    <item>
      <title>Case Report: Pediatric Hallucinations and Anti-Neuronal Intermediate Filament Autoimmune Encephalitis</title>
      <link>https://escholarship.org/uc/item/5nc3w288</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Patients with psychiatric concerns often present to an emergency department (ED) for medical evaluation prior to inpatient psychiatry placement. One diagnosis to consider prior to disposition is autoimmune encephalitis (AIE). This report describes a pediatric patient who presented with psychiatric symptoms that required inpatient admission and workup to diagnose a rare form of AIE.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 16-year-old female with no known past medical history presented as a transfer from an outside hospital for medical evaluation of two days of auditory and visual hallucinations. Initial labs and imaging were unremarkable. Due to the acuity of her symptoms and abnormal vital signs, she was admitted to the hospital for further medical workup. After almost three weeks inpatient and multiple specialist consultations, she was diagnosed with anti-heavy chain neuronal intermediate filament AIE. The next month of admission included treatment...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5nc3w288</guid>
      <pubDate>Thu, 1 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Bjornstad, Amanda</name>
      </author>
      <author>
        <name>Oberhauser-Lim, Natalie</name>
      </author>
      <author>
        <name>Phan, Tammy</name>
      </author>
      <author>
        <name>Samones, Emmelyn</name>
      </author>
      <author>
        <name>Young, Tim</name>
      </author>
    </item>
    <item>
      <title>Phantom Arm Pain and Tinnitus in a Patient with ST-Segment&amp;nbsp;Elevation Myocardial Infarction: A Case Report</title>
      <link>https://escholarship.org/uc/item/63z929k8</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;We present the case of a patient with the unusual occurrence of phantom arm&amp;nbsp;pain and an acute exacerbation of chronic tinnitus during an ST-segment elevation myocardial&amp;nbsp;infarction (STEMI).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 56-year-old man was having several classic symptoms associated with acute&amp;nbsp;coronary syndrome, along with perceived pain in an arm lost years earlier in a traumatic accident&amp;nbsp;and a sudden worsening of his chronic tinnitus. Emergency medical services responded and&amp;nbsp;diagnosed a STEMI on scene. A 100% occlusion of his right coronary artery was rapidly identified&amp;nbsp;in the hospital and treated with the deployment of two drug-eluting stents. After the procedure his&amp;nbsp;symptoms resolved. He was discharged without incident two days later.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;Whereas arm pain is a well-documented presenting symptom of acute coronary&amp;nbsp;syndrome, phantom limb pain and exacerbation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/63z929k8</guid>
      <pubDate>Tue, 16 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Porter, John</name>
      </author>
      <author>
        <name>Liedl, Chad P.</name>
      </author>
      <author>
        <name>Steever, Kevin P.</name>
      </author>
      <author>
        <name>Lumby, Hunter D.</name>
      </author>
      <author>
        <name>Hanson, Chase M.</name>
      </author>
      <author>
        <name>Vaden, Hannah Rae R.</name>
      </author>
      <author>
        <name>Klassen, Aaron</name>
      </author>
    </item>
    <item>
      <title>Ewing Sarcoma in the Cervical Spine Causing Left Lower&amp;nbsp;Extremity Hemiparesis and Left Upper Extremity Hemiplegia:&amp;nbsp;A Case Report</title>
      <link>https://escholarship.org/uc/item/1ns354pg</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Ewing sarcoma is a relatively common neoplasm occurring in pediatric patients 10-20&amp;nbsp;years of age, commonly presenting with bone fracture, fever, and pain and swelling at the site of the&amp;nbsp;primary tumor. Here we present an unusual case of Ewing sarcoma in the cervical spine leading to&amp;nbsp;neurological symptoms including left lower extremity hemiparesis and left upper extremity hemiplegia.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 19-year-old Bengali-speaking male presented to the emergency department with&amp;nbsp;a three-week history of left lower extremity hemiparesis and left upper extremity hemiplegia. Due to&amp;nbsp;concern for spinal cord compression, a computed tomography of the cervical spine without contrast was&amp;nbsp;obtained, which revealed a lucent lesion in the left fifth cervical (C5) vertebral body. Magnetic resonance&amp;nbsp;imaging of the cervical spine revealed a left cervical extradural mass present from C3-C7. The patient&amp;nbsp;subsequently...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ns354pg</guid>
      <pubDate>Wed, 10 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Adler, Alexander</name>
      </author>
      <author>
        <name>Messman, Anne</name>
      </author>
    </item>
    <item>
      <title>Implanted in the Scar: A Case Report of Diagnosis and&amp;nbsp;Management of Cesarean Scar Ectopic Pregnancy</title>
      <link>https://escholarship.org/uc/item/1nk255m4</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Ectopic pregnancy is a serious pregnancy complication that occurs when a gestational&amp;nbsp;sac implants outside the uterus, most commonly in the fallopian tubes. However, a rare form of&amp;nbsp;ectopic pregnancy, the cesarean scar ectopic pregnancy, occurs within a prior cesarean section&amp;nbsp;scar and is becoming more common as cesarean delivery rates continue to rise. Cesarean scar&amp;nbsp;ectopic pregnancies are challenging to diagnose and pose significant risks, including rupture and&amp;nbsp;hemorrhage, which can lead to maternal death.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 27-year-old woman presented to the emergency department with a 16-day history of&amp;nbsp;abdominal pain and vaginal bleeding, initially believed to be her menstrual period. She had a history&amp;nbsp;of one previous lower uterine segment cesarean section. On examination, her beta-human chorionic&amp;nbsp;gonadotropin (β-hCG) levels were elevated, and transvaginal ultrasound revealed an empty...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1nk255m4</guid>
      <pubDate>Wed, 10 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schindler, Hanna</name>
      </author>
      <author>
        <name>Keeler, Leila</name>
      </author>
    </item>
    <item>
      <title>Potassium Overdose in Patient with Chronic Kidney Disease&amp;nbsp;on Losartan: A Case Report</title>
      <link>https://escholarship.org/uc/item/41h5t3zv</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Hyperkalemic emergencies can present with weakness, paralysis, sensorimotor&amp;nbsp;deficits, and potentially fatal cardiac conduction abnormalities even in the absence of an elevated&amp;nbsp;serum potassium. Common antihypertensive medications, such as angiotensin-converting enzyme&amp;nbsp;inhibitors or angiotensin II receptor blockers, are associated with serum potassium elevations and&amp;nbsp;can exacerbate hyperkalemia, especially in patients with renal impairment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We report a 49-year-old patient who presented to the emergency department six&amp;nbsp;hours following an intentional ingestion of potassium supplements totaling 600 milliequivalents&amp;nbsp;(mEq). The patient also reported chronic use of ibuprofen and losartan 50 mg. Symptoms on&amp;nbsp;presentation included weakness, chest pain, and shortness of breath. Initial labs revealed a&amp;nbsp;potassium &amp;gt; 10 mEq/L which was beyond the upper limit of assay detection...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/41h5t3zv</guid>
      <pubDate>Mon, 8 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Naseem, Ahmed</name>
      </author>
      <author>
        <name>Schoenborn, Mark</name>
      </author>
      <author>
        <name>Scheidler, James</name>
      </author>
      <author>
        <name>Barclay, William</name>
      </author>
      <author>
        <name>Volk, Garrett</name>
      </author>
    </item>
    <item>
      <title>70-year-old Woman with Chest Tightness and Shortness of Breath</title>
      <link>https://escholarship.org/uc/item/5dk3f72j</link>
      <description>&lt;p&gt;Chest tightness and shortness of breath are relatively common reasons for presentation to the&amp;nbsp;emergency department (ED), often triggering protocolized workups and dispositions. A good history,&amp;nbsp;however, can reveal additional elements that may dramatically alter the differential diagnosis and&amp;nbsp;management. A 70-year-old woman presented to the ED complaining of subacute chest tightness&amp;nbsp;with dyspnea on exertion. This case offers a thoughtful analysis of how to integrate key findings&amp;nbsp;within a patient’s history, exam, and workup in the ED. The surprising final diagnosis and case&amp;nbsp;outcome are then revealed.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5dk3f72j</guid>
      <pubDate>Sun, 7 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dunn, Robert E</name>
      </author>
      <author>
        <name>Klucher, Brianna</name>
      </author>
      <author>
        <name>Bontempo, Laura J</name>
      </author>
      <author>
        <name>Gatz, John David</name>
        <uri>https://orcid.org/0000-0002-3380-2419</uri>
      </author>
    </item>
    <item>
      <title>Acute Hypercapnic Respiratory Failure from Foreign Body Aspiration in a 16-Month-Old: A Case Report</title>
      <link>https://escholarship.org/uc/item/1xf3f47b</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Acute hypercapnic respiratory failure secondary to foreign body aspiration is a rare&amp;nbsp;but severe complication seen in pediatric patients. Foreign body aspiration is one of the leading&amp;nbsp;causes of death in children and requires prompt intervention and stabilization when definitive&amp;nbsp;bronchoscopy is not readily available.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We describe the case of a 16-month-old male who developed acute hypercapnic&amp;nbsp;respiratory failure following the aspiration of a foreign body. On presentation to the emergency&amp;nbsp;department, the child was in respiratory distress, appeared cyanotic, and had severely impaired&amp;nbsp;oxygenation, all indicating respiratory failure. Initial management involved stabilization, advanced&amp;nbsp;airway management, and ventilatory adjustments. Efficient communication with multiple specialists&lt;br&gt;coordinated the appropriate transfer of the patient to a tertiary pediatric facility for bronchoscopy...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1xf3f47b</guid>
      <pubDate>Sun, 7 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Sabrina</name>
      </author>
      <author>
        <name>Combs, Kallie</name>
      </author>
      <author>
        <name>Shin, Richard</name>
      </author>
    </item>
    <item>
      <title>Insect in the Ear- Response and Treatment of an Uncommon Prehospital Emergency: A Case Report</title>
      <link>https://escholarship.org/uc/item/6f29p8pj</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Foreign bodies in the external auditory canal are an uncommon presentation in&amp;nbsp;emergency settings. Among adults, insects represent a frequent organic foreign body, often causing&amp;nbsp;symptoms such as otalgia, tinnitus, vertigo, and anxiety. Prehospital management of such cases is&amp;nbsp;rarely addressed in the medical literature, with minimal guidance available for emergency medical&amp;nbsp;services (EMS) personnel. In this report we discuss their role in stabilizing patients and reducing&amp;nbsp;discomfort through appropriate interventions.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 40-year-old male called EMS after a live insect entered his left ear, causing severe&amp;nbsp;otalgia and distress. Prehospital medical personnel clinically confirmed the presence of the insect&amp;nbsp;and assessed for signs of tympanic membrane perforation. A medical command physician authorized&amp;nbsp;the use of 2% lidocaine to euthanize the insect, which alleviated movement-related...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6f29p8pj</guid>
      <pubDate>Wed, 26 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Bashline, Colin</name>
        <uri>https://orcid.org/0009-0005-7926-2859</uri>
      </author>
      <author>
        <name>Jester, Matthew</name>
      </author>
      <author>
        <name>Morris, Christopher</name>
      </author>
    </item>
    <item>
      <title>Diagnosing Temporal Lobe Epilepsy in the Emergency Department: A Case Report</title>
      <link>https://escholarship.org/uc/item/3pm5r47t</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Temporal lobe epilepsy is a form of focal epilepsy that originates in the temporal lobes,&amp;nbsp;often presenting with a variety of symptoms including altered consciousness, automatisms, and&amp;nbsp;focal seizures with or without impaired awareness. Given such a diversity of manifesting symptoms,&amp;nbsp;recognizing temporal lobe epilepsy in the emergency department (ED) can be challenging. Early&amp;nbsp;identification is crucial for appropriate management, including timely initiation of antiepileptic therapy&amp;nbsp;and differentiation from other neurological emergencies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 50-year-old male with no prior history of seizures or neurological conditions&amp;nbsp;presented to the ED after experiencing unusual sensations that had begun three days earlier. The&amp;nbsp;patient described an intermittent sensation of warmth rising from his pelvis to his head, accompanied&amp;nbsp;by an experiential déjà vu-like feeling he described as “dream...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3pm5r47t</guid>
      <pubDate>Sat, 22 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Felker, Ashlynn Alexandria</name>
      </author>
      <author>
        <name>Tanner, Jason</name>
      </author>
    </item>
    <item>
      <title>Sonographic Evaluation of an Inguinal Bubo from&lt;em&gt;&amp;nbsp;Bartonella&amp;nbsp;henselae&lt;/em&gt;: A Case Report</title>
      <link>https://escholarship.org/uc/item/6mb946wd</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Emergency physicians can use point-of-care ultrasound (POCUS) to identify lymph nodes in certain clinical scenarios, and advanced users can determine significant information (such as concerns for malignancy or differentiating them from abscesses for incision and drainage) based on a large volume of literature and images associated with those pathologies. However, current&amp;nbsp;literature does not contain a similar volume of images and cases of suppurative lymph nodes, or&amp;nbsp;buboes, limiting the ability to make the diagnosis sonographically at the bedside.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;We report on a man who presented to the emergency department (ED) with a worsening inguinal mass that changed size with positioning, as well as a 20-pound weight loss&amp;nbsp;occurring over the course of a month. Point-of-care ultrasound of the mass was concerning for&amp;nbsp;a necrotic suppurative lymph node, which was further evaluated with cross-sectional imaging.&amp;nbsp;The...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6mb946wd</guid>
      <pubDate>Mon, 17 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Campillo Luna, Julian</name>
        <uri>https://orcid.org/0000-0001-8509-0700</uri>
      </author>
      <author>
        <name>Shaffer, Robert Woodworth</name>
      </author>
    </item>
    <item>
      <title>Heed The Warning: A Case Report on Capsular&amp;nbsp;Warning Syndrome</title>
      <link>https://escholarship.org/uc/item/5s53776r</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Evaluating patients with acute neurologic deficits is a regular occurrence in the&amp;nbsp;emergency department (ED), but some presentations warrant increased concern.&amp;nbsp;This case&amp;nbsp;highlights the importance of repeat evaluations and how resolution of symptoms does not rule out a&amp;nbsp;more ominous underlying pathology.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: A 59-year-old male with a past medical history of coronary artery disease and Human&amp;nbsp;immunodeficiency viruses (HIV) presented to a Level II trauma and comprehensive stroke center&amp;nbsp;for left-sided facial droop and left- sided hemiparesis. Computed tomography of the brain including&amp;nbsp;angiography and perfusion was performed revealing no hemorrhage or large vessel occlusion. Given&amp;nbsp;his National Institutes of Health Stroke Scale score of 11, he received alteplase and subsequently&amp;nbsp;experienced several episodes of resolution and recurrence of his symptoms while in the ED.&amp;nbsp;Magnetic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5s53776r</guid>
      <pubDate>Mon, 17 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Tarahomi, Targol</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>Pediatric Pisiform Dislocation: A Case Report</title>
      <link>https://escholarship.org/uc/item/0g21p50z</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Dislocations of the pisiform bone are rare, and literature on this injury is sparse. The&amp;nbsp;uncommon nature of this condition, as well as limited data, makes recognition and diagnosis difficult,&amp;nbsp;increasing the chances these injuries may be overlooked. Missing this diagnosis can lead to pain,&amp;nbsp;reduced joint function, and nerve damage.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report&lt;/strong&gt;: We present a case of pediatric pisiform dislocation and discuss the diagnosis and&amp;nbsp;treatment in an emergency department setting.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: Prompt diagnosis and treatment of pisiform dislocations are vital to ensure favorable&amp;nbsp;outcomes.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0g21p50z</guid>
      <pubDate>Mon, 17 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wahhab, John</name>
      </author>
      <author>
        <name>Vimalan Jeya, Iswarya</name>
      </author>
      <author>
        <name>Huttner, Jackson Robert</name>
      </author>
    </item>
    <item>
      <title>Amphetamine-induced Reverse Takotsubo Cardiomyopathy&amp;nbsp;and Thrombosis: A Case Report</title>
      <link>https://escholarship.org/uc/item/3mx9n0xk</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Takotsubo cardiomyopathy is characterized by stress-induced left ventricular&amp;nbsp;dysfunction. The reverse form accounts for &amp;lt; 25% of all cases. We present a case of reverse&amp;nbsp;Takotsubo cardiomyopathy in a young, otherwise healthy, woman following illicit drug use.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Report: &lt;/strong&gt;A 19-year-old female patient presented to the emergency department (ED) complainingof insomnia, left-sided chest pain, palpitations, and heightened energy levels after ingesting a significant&amp;nbsp;quantity of small, rounded chocolate chips containing unidentified pills at a rave party the previous&amp;nbsp;night. Her electrocardiogram revealed sinus tachycardia with ST-segment elevation in leads I and aVL.&amp;nbsp;At the ED she developed respiratory distress and required oxygen supplementation. Her troponin level&amp;nbsp;was 1.048 nanograms per milliliter (ng/mL) (reference range &amp;lt; 0.03 ng/mL), and her urine drug screen&lt;br&gt;was positive for methamphetamines....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3mx9n0xk</guid>
      <pubDate>Mon, 3 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Rabil, Anthony</name>
      </author>
      <author>
        <name>Fakhereddine, Omar</name>
      </author>
      <author>
        <name>Rebeiz, Abdallah</name>
      </author>
      <author>
        <name>El Zahran, Tharwat</name>
      </author>
    </item>
    <item>
      <title>CPC-EM Full-Text Issue</title>
      <link>https://escholarship.org/uc/item/87j9p168</link>
      <description>&lt;p&gt;n/a&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/87j9p168</guid>
      <pubDate>Sat, 1 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>CPC-EM, Clinical Practice and Cases in Emergency Medicine</name>
      </author>
    </item>
    <item>
      <title>Use of Point-of-Care Ultrasound for Detection of Urethral Foreign Bodies: A Case Series</title>
      <link>https://escholarship.org/uc/item/8qg4d2cf</link>
      <description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;:&amp;nbsp;Urethral foreign bodies are an uncommon presentation in the emergency department&amp;nbsp;(ED) and can be difficult to assess and diagnose. There are examples in the literature of ultrasound&amp;nbsp;detecting urethral foreign bodies. While not standard of practice, point-of-care ultrasound (POCUS)&amp;nbsp;may be a useful tool for this unique pathology.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Case Series: &lt;/strong&gt;We describe three cases in which POCUS was used in the care of patients presenting&amp;nbsp;with urethral foreign bodies. Ultrasound aided in diagnosis and helped facilitate further management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;:&amp;nbsp;While urethral foreign bodies are relatively uncommon, they can lead to significant&amp;nbsp;morbidity, which makes their prompt identification and treatment important. Ultrasound provides&amp;nbsp;a rapid means of evaluation that allows the patient to stay under observation by ED staff while&amp;nbsp;removing exposure to radiation or contrast.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8qg4d2cf</guid>
      <pubDate>Fri, 24 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Tomasi, Luca</name>
      </author>
      <author>
        <name>Zampi, Michael</name>
      </author>
      <author>
        <name>Schroeder, Michele L</name>
      </author>
      <author>
        <name>Cooper, Michael</name>
      </author>
      <author>
        <name>McIntyre, Norah</name>
      </author>
    </item>
  </channel>
</rss>
