A case of white sponge nevus in the oral cavity.

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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 oral white sponge nevus--a rare hereditary condition.

White sponge nevus (WSN) is an autosomal dominant skin disorder characterized by white, corrugated and diffuse plaques mainly affecting the oral mucosa. The condition has a high penetrance and variable expressivity, but familial reports are uncommon. This report presents a familial case of WSN in which two sisters are affected by the disorder.

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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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ژورنال

عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery

سال: 1996

ISSN: 2186-1579,0021-5163

DOI: 10.5794/jjoms.42.308