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首页> 外文期刊>Frontiers in Neurology >Alopecia Universalis following Alemtuzumab Treatment in Multiple Sclerosis: A Barely Recognized Manifestation of Secondary Autoimmunity—Report of a Case and Review of the Literature
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Alopecia Universalis following Alemtuzumab Treatment in Multiple Sclerosis: A Barely Recognized Manifestation of Secondary Autoimmunity—Report of a Case and Review of the Literature

机译:Alemtuzumab治疗多发性硬化症后的通用脱发:几乎公认的继发性自身免疫性表现—病例报告和文献复习

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摘要

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.
机译:继发性自身免疫是几乎所有其他接受alemtuzumab治疗的多发性硬化症患者中最常见的不良事件。我们报告了一例患有复发缓解型多发性硬化症的患者,该患者在第二次使用alemtuzumab的治疗后6个月,在两个大腿上均报告了平滑的圆形完全脱发的圆形区域。该患者被诊断患有斑秃(AA)。在3个月内,AA逐渐完全消失(全身性脱发)。当前文献很少将阿仑单抗与自身免疫性脱发的发生联系起来。在这里,我们报告了一种影响皮肤的鲜为人知的自身免疫性疾病,很可能与阿仑单抗有关。我们强调需要对尚未接受描述的自身免疫性疾病进行阿仑单抗治疗的患者进行仔细的临床监测。

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