拉叙厄-格雷厄姆-利特尔-皮卡迪综合征：20年随访

Lassueur-Graham Little-Piccardi syndrome: a 20-year follow-up.

作者信息

Ghislain Pierre-Dominique, Van Eeckhout Pascal, Ghislain Emile

出版信息

Dermatology. 2003;206(4):391-2. doi: 10.1159/000069966.

Abstract

Lassueur-Graham Little-Piccardi (LGLP) syndrome is a distinctive entity associating a scarring patchy alopecia of the scalp, a non-cicatricial axillary and pubic hair loss and a lichenoid follicular eruption. We present a 20-year follow-up of a demonstrative case, which had begun as typical lichen planus. In the literature, the relationship with lichen planus remains unclear. The diagnosis of LGLP syndrome should be evoked for all scarring alopecias.

摘要

拉叙厄-格雷厄姆·利特尔-皮卡迪（LGLP）综合征是一种独特的病症，伴有头皮瘢痕性斑片状脱发、非瘢痕性腋窝和耻骨部毛发脱落以及苔藓样毛囊疹。我们展示了一例典型扁平苔藓起病病例的20年随访情况。在文献中，其与扁平苔藓的关系仍不明确。对于所有瘢痕性脱发都应考虑LGLP综合征的诊断。