Bilenchi R, Pisani C, Poggiali S, Andreassi A, de Padova L A, di Perrit T
Department of Clinical Medicine and Immunological Sciences, Section of Dermatology, University of Siena, Siena, Italy.
Lupus. 2004;13(10):815-6. doi: 10.1191/0961203304lu1062cr.
Genital involvement is a rare manifestation in discoid lupus erythematosus (DLE) and systemic lupus erythematosus (SLE), and there are few reports on vulvar clinical features. We describe a 41-year old Caucasian woman with bilateral vulvar DLE. Although vulvar lesions in lupus are probably more common than is realized, the present report is the first case of genital DLE documented in a female.
生殖器受累在盘状红斑狼疮（DLE）和系统性红斑狼疮（SLE）中是一种罕见的表现，关于外阴临床特征的报道很少。我们描述了一名41岁的白种女性，患有双侧外阴DLE。尽管狼疮中的外阴病变可能比人们意识到的更为常见，但本报告是首例记录在女性中的生殖器DLE病例。
