Unilateral systematized linear porokeratosis: A report of a rare case
نویسندگان
چکیده
منابع مشابه
Unilateral linear Syringoma: A case report
Syringoma is a benign tumor arising from intra-epidermal ducts of eccrine sweat glands. It usually presents as small translucent papules on eyelids and upper cheeks. The case, which is presented, is a rare from of syringoma that occurred in a linear fashion on the trunk. Dermatologists should be aware of such form of syringoma to differentiate it from other similar lesions. This 23 year-o...
متن کاملLinear porokeratosis: a case report
Porokeratosis is a rare genodermatosis based on chronic keratinization disorder histologically characterized by the presence of a cornoid lamella and various clinical manifestations. Five most commonly described types of poroketarosis are porokeratosis of Mibelli or ”classic” porokeratosis, disseminated superfi cial actinic porokeratosis, disseminated palmoplantar porokeratosis, linear porokera...
متن کاملUnilateral punctate porokeratosis - Case report*
This case report involves a 20-year-old man with unilateral punctate porokeratosis. The patient presented an 8-year history of numerous asymptomatic keratotic papules and pits with linear distribution on his left pal-mar surface and fifth finger of the left hand. Histopathological examination of the keratotic plug revealed findings of distinct epidermal depressions containing cornoid lamellae. ...
متن کاملVerrucous porokeratosis: A case report
Porokeratoses are uncommon hereditary or acquired keratinization disorders due to abnormal clones of keratinocytes in the epidermis. Porokeratoses have several clinical features which may occur simultaneously. A rare type is verrucous porokeratosis (VPK). Herein, we present a 47-year-old man with a 4-year history of perianal verrucous lesions and one year history of annular pruritic lesions on ...
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: Indian Journal of Dermatology
سال: 2011
ISSN: 0019-5154
DOI: 10.4103/0019-5154.84725