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一名成人的遗传性肠病性肢端皮炎

Hereditary acrodermatitis enteropathica in an adult.

作者信息

Graves K, Kestenbaum T, Kalivas J

出版信息

Arch Dermatol. 1980 May;116(5):562-4.

PMID:7377790
Abstract

The condition of a 33-year-old woman who had a history of blisters following trauma on the hands, knees, and feet since 1 year of age previously had been diagnosed as epidermolysis bullosa. She also had psoriasiform plaques, a pustular crusted periorificial eruption, paronychia, alopecia, and photophobia. She had had minimal history of diarrhea. A markedly decreased serum zinc level was found, and treatment with zinc sulfate was instituted, resulting in clearing of all clinical manifestations. Since patients with hereditary acrodermatitis enteropathica may have minimal or no diarrhea and the correct diagnosis may be long delayed, the condition should not be considered strictly a disease of children.

摘要

一名33岁女性,自1岁起手部、膝盖和足部受伤后出现水疱,此前被诊断为大疱性表皮松解症。她还患有银屑病样斑块、脓疱结痂性口周皮疹、甲沟炎、脱发和畏光。她腹泻病史轻微。发现血清锌水平显著降低,遂开始用硫酸锌治疗,所有临床表现均消退。由于遗传性肠病性肢端皮炎患者可能腹泻轻微或无腹泻,正确诊断可能会延迟很久,因此该病不应被严格视为儿童疾病。

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