伴有脱发的光分布性苔藓样变:格雷厄姆-利特尔-皮卡迪-拉瑟尔综合征的独特表现

Q2 Medicine
International Journal of Trichology Pub Date : 2023-07-01 Epub Date: 2024-04-05 DOI:10.4103/ijt.ijt_47_22
Austin Ambur, Aashni Bhukhan, Charles Dunn, Rajiv Nathoo
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引用次数: 0

摘要

格雷厄姆-利特尔-皮卡迪-拉瑟尔综合征(GLPLS)的特征是弥漫性脱发和影响头皮、眉毛和三叉神经间区域的苔藓样毛囊性糜烂。它被认为是扁平苔藓的一种变异型。这种病通常先在躯干和四肢出现角化过度的丘疹,然后发展为脱发。有几种亚型的扁平苔藓与光敏性糜烂有关,包括类苔藓药物反应、光化性扁平苔藓和色素性扁平苔藓;但目前还没有与 GLPLS 相关的病例报道。我们在此报告首例显示光分布性苔藓样疹子的 GLPLS 病例,以扩大光加重病症的鉴别诊断范围。我们还通过这个病例回顾了病理生理学和治疗 GLPLS 的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photodistributed Lichenoid Eruption with Alopecia: A Unique Presentation of Graham-Little-Piccardi-Lasseur Syndrome.

Graham-Little-Piccardi-Lasseur syndrome (GLPLS) is characterized by diffuse alopecia and a lichenoid follicular eruption affecting the scalp, eyebrows, and intertriginous regions. It is considered a variant of lichen planopilaris. The condition often begins as hyperkeratotic papules on the trunk and extremities followed by the development of alopecia. Several subtypes of lichen planus have been associated with a photodistriubuted eruption including lichenoid drug reactions, actinic lichen planus, and lichen planus pigmentosus; however, there are no reported cases associated with GLPLS. We herein report the first case of GLPLS displaying a photodistributed lichenoid eruption to expand upon the differential diagnosis of photoaggravated conditions. We also use this case to review the pathophysiology and therapeutic modalities to manage GLPLS.

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CiteScore
1.50
自引率
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发文量
38
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