Punch grafting in lichen sclerosus et atrophicus.
نویسندگان
چکیده
منابع مشابه
Association of Porokeratosis, Vitiligo, Lichen Sclerosus et Atrophicus and Lichen Planus: A case report
Although lichen planus and vitiligo are common skin disorders, their association with two other uncommon diseases, i.e. lichen sclerosus et atrophicus and disseminated superficial actinic porokeratosis, seems to be a very rare occurrence. We report herein a 70-year-old man who developed all of these four skin disorders simultaneously.
متن کاملMicrosoft Word - DRM412BF
Punch grafting Lichen sclerosus et atrophicus Dr. Subrata Malakar, P-158, CIT Scheme VI M, Kankurgachi, Calcutta-700054 (India) Lichen sclerosus et atrophicus (LSA) is a disease of unknown etiology characterized by porcelain-white sclerotic patches of skin with frequent involvement of male and female genitalia [ 1 ]. The condition often coexists with morphea and systemic sclerosis [2, 3]. Howev...
متن کاملLichen planus leading to panurethral stricture: A rare case report with review of literature
Lichen planus is a papulosquamous disorder of skin. Genital lichen planus is self limiting disease that resolves without any consequences. Although Lichen planus may coexist with lichen sclerosus et atrophicus, such association in genitalia is not reported so far. We report a case of a forty years old man, presented with a papulosquamous lesion over the prepuce four years back and then he subse...
متن کاملLichen sclerosus et atrophicus in children.
The symptoms, findings, associated conditions, and treatment of lichen sclerosus et atrophicus were studied in 10 girls and one boy. Lichen sclerosus et atrophicus is a benign but chronic condition of the anogenital area of girls and, less frequently, of boys. The characteristic lesions are hypo-pigmented plaques in a figure-of-8 pattern surrounding the vulva and anus and often involving the na...
متن کاملCarcinoma of the penis developed in lichen sclerosus et atrophicus.
Malignant change developing in lichen sclerosus et atrophicus is rare in men. A case is described in a 39-year-old man.
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ورودعنوان ژورنال:
- Dermatology
دوره 195 4 شماره
صفحات -
تاریخ انتشار 1997