格雷厄姆-利特尔-皮卡迪-拉苏尔综合征伴粘膜受累:罕见病例

Q2 Medicine
International Journal of Trichology Pub Date : 2023-11-01 Epub Date: 2024-10-07 DOI:10.4103/ijt.ijt_88_22
Rutoo Vipulkumar Polra, Jinal Jainendrabhai Tandel, Pragya Ashok Nair
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引用次数: 0

摘要

格雷厄姆-利特尔-皮卡迪-拉苏尔综合征(GLPLS)是一种扁平苔藓。它主要影响 40-60 岁的女性。其特征为头皮斑片状卡他性脱发、腋窝和腹股沟非卡他性脱发以及身体、头皮或两者上的毛囊性棘丘疹三联征。诊断的依据是临床病理相关性。目前有不同的治疗方法,但效果并不理想,因此必须及早诊断,以防止病情恶化和瘢痕性脱发。本文介绍了一例 GLPLS 病例,患者是一名 73 岁的女性,其临床、皮肤镜和组织病理学检查均具有典型特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graham-Little-Piccardi-Lassueur Syndrome with Mucosal Involvement: A Rare Case.

Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a type of lichen planopilaris. It mainly affects females aged 40-60 years. It is characterized by the triad of patchy cicatricial alopecia of the scalp, noncicatricial alopecia of the axilla and groin and a follicular spinous papule on the body, scalp, or both. The diagnosis is based on clinicopathological correlation. Different modalities of treatment are available with unsatisfactory responses, so early diagnosis is necessary to prevent progression and scarring alopecia. A case of GLPLS with classical features on clinical, dermoscopic, and histopathological examination is presented in a 73-year-old female.

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CiteScore
1.50
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