Alopecia Mimicking Lichen Planopilaris in a Patient with Mycosis Fungoides.

IF 1.4 Q3 DERMATOLOGY
Skin Appendage Disorders Pub Date : 2025-06-01 Epub Date: 2024-12-28 DOI:10.1159/000543256
Daniel Asz-Sigall, Marysol Macedo Perez, Rosa María Lacy-Niebla, Carlos Barrera-Ochoa, Roberto Arenas, Sonia Toussaint-Caire, Diana Santamaría-Domínguez, Diana Valeria Guerrero-Hernández, Irene M Rodríguez-Escamilla, Eduardo Corona-Rodarte
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引用次数: 0

Abstract

Introduction: Mycosis fungoides (MF), the most common form of primary cutaneous T-cell lymphoma, can present with diverse clinical manifestations, including alopecia that mimics conditions such as alopecia areata (AA) and lichen planopilaris (LPP). The folliculotropic variant (FMF) poses diagnostic challenges due to overlapping clinical features, necessitating histopathological evaluation for accurate diagnosis.

Case report: A 58-year-old woman with a 21-year history of stage IB MF developed alopecic patches in the left temporoparietal region, accompanied by pruritus and trichodynia. Physical examination revealed scarring and non-scarring alopecic patches, while trichoscopy showed characteristic features of follicular involvement. Histological analysis confirmed a diagnosis of FMF, characterized by atypical lymphocytic infiltrate and follicular destruction. Treatment included maintenance of NB-UVB and isotretinoin, with the addition of monthly intralesional corticosteroid injections, resulting in symptomatic improvement.

Discussion/conclusion: This case highlights the diagnostic challenges posed by FMF mimicking AA and LPP. The overlap in clinical and trichoscopic findings underscores the necessity for histopathological evaluation to confirm FMF and differentiate it from other alopecic conditions. Early recognition and a multidisciplinary approach to treatment are crucial for improving outcomes in patients with this aggressive variant of MF.

蕈样真菌病患者的模拟扁平苔藓性脱发。
简介:蕈样真菌病(MF)是原发性皮肤t细胞淋巴瘤最常见的形式,可呈现多种临床表现,包括类似斑秃(AA)和扁平苔藓(LPP)的脱发。由于临床特征重叠,促卵泡变异体(FMF)提出了诊断挑战,需要组织病理学评估才能准确诊断。病例报告:一名58岁女性,有21年的IB期MF病史,左侧颞顶区出现脱发斑块,伴有瘙痒和头痛症。体格检查显示瘢痕性和非瘢痕性脱发斑块,而毛发镜检查显示毛囊受累的特征。组织学分析证实了FMF的诊断,以非典型淋巴细胞浸润和滤泡破坏为特征。治疗包括维持NB-UVB和异维甲酸,并每月增加局部注射皮质类固醇,导致症状改善。讨论/结论:本病例强调了FMF模拟AA和LPP所带来的诊断挑战。临床和毛镜检查结果的重叠强调了组织病理学评估的必要性,以确认FMF并将其与其他脱发状况区分开来。早期识别和多学科治疗对于改善这种侵袭性MF变型患者的预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
10.00%
发文量
69
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