منابع مشابه
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...
متن کاملWhite 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.
متن کاملwhite 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.
متن کاملFamilial 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...
متن کاملKeratin 13 mutations associated with oral white sponge nevus in two Chinese families
White sponge nevus (WSN) is an autosomal dominant hereditary disease. Keratin 4 (KRT4) and Keratin 13 (KRT13) gene mutations were involved in the WSN. We recruited two WSN Chinese families, and oral lesion biopsy with hematoxylin and eosin staining showed that patients had significant pathological characteristics. The mutations of KRT4 and KRT13 gene were detected by PCR and direct sequencing. ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery
سال: 1981
ISSN: 2186-1579,0021-5163
DOI: 10.5794/jjoms.27.732