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阿仑单抗治疗多发性硬化后出现全秃:继发性自身免疫的一种罕见表现——1例报告及文献复习

Alopecia Universalis following Alemtuzumab Treatment in Multiple Sclerosis: A Barely Recognized Manifestation of Secondary Autoimmunity-Report of a Case and Review of the Literature.

作者信息

Zimmermann Julian, Buhl Timo, Müller Marcus

机构信息

Department of Neurology, Universitätsklinikum Bonn, Bonn, Germany.

Department of Dermatology, Venereology and Allergology, University Medical Center Göttingen, Göttingen, Germany.

出版信息

Front Neurol. 2017 Oct 30;8:569. doi: 10.3389/fneur.2017.00569. eCollection 2017.

Abstract

Secondary autoimmunity is the most frequent adverse event occurring in almost every other alemtuzumab-treated multiple sclerosis patient. We report a case of a patient with relapsing-remitting multiple sclerosis who reported smooth, circular areas of complete hair loss on both thighs 6 months after the second treatment cycle with alemtuzumab. The patient was diagnosed as having alopecia areata (AA). Within 3 months, AA progressed to complete loss of all body hair (alopecia universalis). Current literature rarely connects alemtuzumab with the onset of alopecia of autoimmune origin. Here, we report a little-noticed autoimmune disease affecting the skin, very likely being associated with alemtuzumab. We emphasize the necessity of careful clinical surveillance of alemtuzumab-treated patients for yet undescribed autoimmune diseases.

摘要

继发性自身免疫是几乎每一位接受阿仑单抗治疗的多发性硬化症患者中最常见的不良事件。我们报告了一例复发缓解型多发性硬化症患者的病例,该患者在接受第二个阿仑单抗治疗周期6个月后,双侧大腿出现了光滑的圆形完全脱发区。该患者被诊断为斑秃(AA)。在3个月内,斑秃进展为全身毛发完全脱落(普秃)。目前的文献很少将阿仑单抗与自身免疫性脱发的发病联系起来。在此,我们报告一种鲜为人知的影响皮肤的自身免疫性疾病,很可能与阿仑单抗有关。我们强调对接受阿仑单抗治疗的患者进行仔细临床监测以发现尚未描述的自身免疫性疾病的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21b/5670499/2438307747af/fneur-08-00569-g001.jpg

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