Lichen sclerosus mistaken for child sexual abuse.
نویسندگان
چکیده
Finally, familial cutaneous collagenoma must be differentiated from two distinct types of eruptive collagenoma. Eruptive collagenoma type 1 is clinically and histologically similar to familial cutaneous collagenoma but without documented familial inheritance. Eruptive collagenoma type 2 presents cutaneous lesions smaller than those of familial cutaneous collagenoma and arranged on the extremities and lower trunk. Both types are histologically characterized by the dermal accumulation of metachromatic, mucinous material, suggesting an actual diagnosis of lichen myxedematosus. 1,9
منابع مشابه
Koebnerization in a Woman with Extragenital Lichen Sclerosus
Lichen sclerosus (LS) is a chronic benign inflammatory disorder of skin and mucosa which affects patients of all age groups, sex and race, particularly caucasian prepubertal girls and postmenopausal women. The etiology of LS is unknown, but it has been suggested that genetic predisposition to inflammatory disorders, immunological constitutions, hormonal influences and local factors might play a...
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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 کاملLichen sclerosus et atrophicus and sexual abuse.
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INTRODUCTION Lichen sclerosus (LS) is a chronic skin disorder with a predilection for the anogenital area. The disease is mostly seen in prepubertal and postmenopausal females. The lesions present as sharply demarcated white plaques encircling the vagina and anus. The atrophic form can lead to scarring of the affected area. MATERIAL AND METHODS Retrospective analysis of hospital records of ch...
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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.
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ورودعنوان ژورنال:
- International journal of dermatology
دوره 44 4 شماره
صفحات -
تاریخ انتشار 2005