Severe Alopecia caused by Azathioprine in Systemic Lupus Erythematosus.

Q3 Medicine
Vijay Kr Rao, Thanushree N, Manasa Rs
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Abstract

Background: Systemic lupus erythematosus (SLE) is an autoimmune disorder with heterogeneous phenotypes. The symptoms range from mild to life-threatening features. Azathioprine (AZA) is a routinely used immunosuppressive agent in mild to moderate SLE. Although bone marrow suppression is reported in AZA usage, severe alopecia is not very common with AZA.

Case description: We report a 45-year-old female with stable clinical and serological lupus maintained on mycophenolate mofetil 500 mg twice per day and hydroxychloroquine 200 mg once per day. She was lost to follow-up with us for >1 year. Since her disease was stable, we switched to AZA 25 mg twice per day to start with and escalated to 50 mg in the morning and 25 mg at night after 2 weeks, with an advice for 4-week follow-up after starting AZA. Hydroxychloroquine was continued at 200 mg once per day. No corticosteroids were used at this time as it was not deemed necessary. Monitoring blood tests for AZA were planned at 4 weeks. She presented at 6 weeks with severe leukopenia as summarized in the table of investigations below and the graph summarizing the trend in leukocyte counts after AZA usage. She was managed in the hospital with intravenous dexamethasone, antibiotic prophylaxis, and hematology consultation, who opined as AZA-induced severe bone marrow suppression and severe alopecia due to AZA. Bone marrow examination was not deemed necessary by the hematologist. AZA was stopped in the hospital and mycophenolate mofetil was prescribed in the immediate follow-up after discharge, as she had previously responded to this drug. Hydroxychloroquine continued throughout her hospital stay. Although her blood counts responded very well after AZA withdrawal, it took nearly 3 months for her to have her normal scalp hair. One of the major differentials that was considered was SLE flare-up, but her clinical features and serology did not support a lupus flare.

Conclusion: Bone marrow suppression is a severe complication of AZA in SLE. Leukopenia and hair loss are the major adverse effects reported during the therapy of AZA. It is sensible to recognize this relationship as prompt diagnosis and treatment is crucial.

硫唑嘌呤引起系统性红斑狼疮的严重脱发。
背景:系统性红斑狼疮(SLE)是一种具有异质性表型的自身免疫性疾病。症状从轻微到危及生命不等。硫唑嘌呤(AZA)是一种常规使用的免疫抑制剂在轻中度SLE。虽然有骨髓抑制的报道,但严重的脱发并不常见。病例描述:我们报告一名45岁女性狼疮患者,临床和血清学稳定,服用霉酚酸酯500 mg每日2次,羟氯喹200 mg每日1次。她失去了与我们的随访,长达110年。由于她的病情稳定,我们开始时改为每天两次25毫克的AZA,两周后逐渐增加到早上50毫克,晚上25毫克,并建议在开始AZA后进行4周的随访。羟氯喹继续200毫克,每天一次。在这个时候没有使用皮质类固醇,因为它被认为是不必要的。计划在第4周进行AZA监测血液检查。她在6周时出现了严重的白细胞减少,如下表所示,图中总结了使用AZA后白细胞计数的趋势。她在医院接受静脉注射地塞米松、抗生素预防和血液学会诊,她认为是AZA引起的严重骨髓抑制和严重脱发。血液学家认为骨髓检查是不必要的。在医院停止了AZA,出院后立即随访开了霉酚酸酯,因为她以前对该药有反应。在她住院期间继续使用羟氯喹。虽然她的血液计数在停用AZA后反应很好,但她花了将近3个月的时间才恢复了正常的头皮头发。其中一个主要的区别被认为是SLE发作,但她的临床特征和血清学不支持狼疮发作。结论:骨髓抑制是AZA治疗SLE的严重并发症。白细胞减少和脱发是在AZA治疗期间报告的主要不良反应。认识到这种关系是明智的,因为及时诊断和治疗至关重要。
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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