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[溃疡性红苔藓。与格雷厄姆-利特尔综合征的鉴别。发病机制与治疗]

[Lichen ruber ulcerosus. Differentiation from Graham-Little syndrome. Pathogenesis and therapy].

作者信息

Lindmaier A, Jurecka W

机构信息

II. Universitäts-Hautklinik Wien.

出版信息

Z Hautkr. 1988 May 15;63(5):439-43.

PMID:3043953
Abstract

A 61-year-old female patient having suffered for several years from typical Graham-Little's syndrome developed lichen ulcerosus after a period of 9 years. We discuss the relationship between these clinical manifestations with special reference to the pathogenesis and distribution of skin lesions in lichen rubber ulcerosus. Among the numerous therapeutic approaches, treatment with chloroquine or dapsone as well as skin grafting seem to be most promising.

摘要

一位患有典型格雷厄姆-利特尔综合征数年的61岁女性患者,在9年后出现了溃疡性扁平苔藓。我们讨论了这些临床表现之间的关系,特别提及了溃疡性扁平苔藓皮肤损害的发病机制和分布。在众多治疗方法中,氯喹或氨苯砜治疗以及皮肤移植似乎最有前景。

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