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Localized Juvenile Spongiotic Gingival Hyperplasia: A Report of 27 Cases.

  • Author(s): Wang, Michael Z
  • Jordan, Richard C
  • et al.

Published Web Location

https://doi.org/10.1111/cup.13549
Abstract

BACKGROUND:Localized juvenile spongiotic gingival hyperplasia (LJSGH) is a poorly understood but distinctive inflammatory hyperplasia occurring in children and young adults. Less than 100 cases have been reported since its initial description. METHODS:During the period of 2015-2018, cases of LJSGH were identified, retrieved and their clinical and histopathological data reviewed. RESULTS:There were 27 cases with a median age of 13 years (range 7-72 years). Twenty-four of 27 patients were less than 20 years old, and in 3 cases the patients were over 60 years of age. The most commonly affected site was the anterior maxillary gingiva presenting as a solitary, red, and papillated lesion. Typical microscopic findings included elevated areas of variably acanthotic, spongiotic non-keratinized epithelium with elongated rete ridges, accompanied by a neutrophilic rich infiltrate. An abrupt transition between epithelium affected by LJSGH and normal mucosa was characteristic. LJSGH typically exhibited full thickness epithelial expression of CK19 without expression of estrogen and progesterone receptors. CONCLUSIONS:The clinical and histopathologic characteristics of LJSGH are unique and consistent. Despite the name, the condition is not limited to juveniles and can occur in adults. LJSGH in adults and juveniles shares the same spectrum of histopathologic and immunohistochemical findings. This article is protected by copyright. All rights reserved.

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