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局限性获得性大疱性表皮松解症累及面部。

Epidermolysis bullosa acquisita localized to the face.

作者信息

Choi G S, Lee E S, Kim S C, Lee S

机构信息

Department of Dermatology, Yonsei University College of Medicine, Yongdong Severance Hospital, Seoul, Korea.

出版信息

J Dermatol. 1998 Jan;25(1):19-22. doi: 10.1111/j.1346-8138.1998.tb02339.x.

Abstract

A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left cheek. The diagnosis of epidermolysis bullosa acquisita was confirmed by means of direct immunofluorescence and direct immunoelectron microscopic studies performed on the perilesional salt-split skin. Topical corticosteroid treatment reduced pruritus and bullae formation. This case of localized epidermolysis bullosa acquisita on the face is reminiscent of Brunsting-Perry cicatricial pemphigoid. We also review the previously reported cases of localized epidermolysis bullosa acquisita.

摘要

一名39岁女性有三年反复出现的大疱性皮疹病史,皮疹局限于左脸颊。通过对皮损周围盐裂皮肤进行直接免疫荧光和直接免疫电子显微镜检查,确诊为获得性大疱性表皮松解症。局部使用皮质类固醇治疗可减轻瘙痒和水疱形成。这例面部局限性获得性大疱性表皮松解症病例让人联想到布伦斯廷 - 佩里瘢痕性类天疱疮。我们还回顾了先前报道的局限性获得性大疱性表皮松解症病例。

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