Two white sponge nevus in a single family: case report

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White sponge nevus: case report.

White sponge nevus (WSN) is a rare oral mucosal lesion first described by Cannon in 1935, characterized as benign leukokeratotic lesion of early onset with periods of remission and exacerbation. It is usually asymptomatic, although pruritus, burning, and pain have been reported following irritating stimuli.WSN is inherited as an autosomal dominant trait with wide variability of expression and h...

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White Sponge Nevus: A Case Report

White sponge nevus (WSN) is a rare hereditary dyskeratotic hyperplasia of mucous membranes. It is an autosomal dominant disorder with variable penetrance. We report a case of WSN in a healthy 21-year-old male with no history of familial involvement. A white smooth plaque with no erythema or other structural abnormalities was observed, which confirmed the diagnosis of WSN histopathologically.

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white sponge nevus: a case report

white sponge nevus (wsn) is a rare hereditary dyskeratotic hyperplasia of mucous membranes. it is an autosomal dominant disorder with variable penetrance. we report a case of wsn in a healthy 21-year-old male with no history of familial involvement. a white smooth plaque with no erythema or other structural abnormalities was observed, which confirmed the diagnosis of wsn histopathologically.

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Familial Case of White Sponge Nevus - Diagnosis and Therapeutical Challenges.

White sponge nevus (WSN) is a rare autosomal dominant disorder with variable penetrance (1). It was first described by Hyde in 1909 (2); in 1935 Cannon named it white sponge nevus (3). Several other names have been applied to this condition: HydeCannon’s disease, familial white folded dysplasia, congenital leukokeratosis mucose oris, hereditary leukokeratosis, and white folded gingivostomatosis...

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A novel keratin 13 variant in a four‐generation family with white sponge nevus

We report a novel KRT13 germ line variant that causes white sponge nevus (WSN) with mucosal dysplasia. Genital, vaginal, and cervical WSN were observed in four female patients, of whom two had premalignant cervical lesions at young age. Two of the 12 patients with oral WSN developed oral squamous cell carcinoma.

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ژورنال

عنوان ژورنال: Journal of Oral Medicine and Oral Surgery

سال: 2020

ISSN: 2608-1326

DOI: 10.1051/mbcb/2020046