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1例与外用糖皮质激素和阿达木单抗联合治疗相关的Majocchi肉芽肿病例报告

A Case Report of Majocchi's Granuloma Associated with Combined Therapy of Topical Steroids and Adalimumab.

作者信息

Chou Wan-Yi, Hsu Chih-Jung

机构信息

From the Department of Dermatology, China Medical University Hospital (W-YC, C-JH); and China Medical University, Taichung, Taiwan (W-YC, C-JH).

出版信息

Medicine (Baltimore). 2016 Jan;95(2):e2245. doi: 10.1097/MD.0000000000002245.

Abstract

Currently, tumor necrosis factor alpha (TNF-alpha) inhibitors are widely used for many autoimmune disorders. However, they cause an immunocompromised status that sometimes leads to many cutaneous side effects including atypical infections. Herein, we report the first case of adalimumab-related Majocchi's granuloma.A 43-year-old Taiwanese male patient with chronic plaque-type psoriasis developed numerous tender nodules 1 month after adalimumab injection. The nodules responded poorly to bacterial folliculitis treatment. After repeated skin biopsies for pathology and tissue fungal culture, Majocchi's granuloma was confirmed. Adalimumab was withheld, and 12 weeks of terbinafine treatment was given. On completion of treatment, the nodular skin lesions and dystrophic nail lesions improved dramatically.The information, including time span, clinical features, histological findings, and improvement following withdrawal of adalimumab and treatment with an oral antifungal agent, indicates that Majocchi's granuloma was adalimumab-related. Psoriasis patients are more susceptible to dermatophyte infection due to local and systemic immunosuppressant therapy. It is important to perform a thorough examination for latent dermatophyte infection, including skin and nail lesions, before treatment with TNF-alpha inhibitors and during traditional psoriasis treatment. When atypical presentation together with treatment failure is noted in psoriasis patients prescribed biologics, clinicians should investigate evidence of dermatophyte infection and provide proper treatment. Sometimes, multiple skin biopsies and tissue fungal cultures are required to establish a correct diagnosis.

摘要

目前,肿瘤坏死因子α(TNF-α)抑制剂被广泛用于多种自身免疫性疾病。然而,它们会导致免疫功能低下状态,有时会引发许多皮肤副作用,包括非典型感染。在此,我们报告首例与阿达木单抗相关的马约基氏肉芽肿病例。一名43岁患有慢性斑块型银屑病的台湾男性患者在注射阿达木单抗1个月后出现大量压痛性结节。这些结节对细菌性毛囊炎治疗反应不佳。经过多次皮肤活检进行病理检查和组织真菌培养后,确诊为马约基氏肉芽肿。停用阿达木单抗,并给予12周的特比萘芬治疗。治疗结束时,结节性皮肤病变和甲营养不良性病变显著改善。包括时间跨度、临床特征、组织学发现以及停用阿达木单抗和口服抗真菌药物治疗后的改善情况等信息表明,马约基氏肉芽肿与阿达木单抗有关。银屑病患者由于局部和全身免疫抑制治疗,更容易发生皮肤癣菌感染。在用TNF-α抑制剂治疗前以及传统银屑病治疗期间,对潜在的皮肤癣菌感染进行全面检查,包括皮肤和指甲病变,非常重要。当给银屑病患者开具生物制剂时,若发现非典型表现且治疗失败,临床医生应调查皮肤癣菌感染的证据并提供适当治疗。有时,需要多次皮肤活检和组织真菌培养才能做出正确诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d80b/4718227/6a5cd10c10bd/medi-95-e2245-g001.jpg

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