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多发性硬化症用阿仑单抗治疗后出现自身免疫性脑炎。

Autoimmune encephalitis following alemtuzumab treatment of multiple sclerosis.

机构信息

Department of Neurology, St Vincent's Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010, Australia.

Department of Radiology, St Vincent's Hospital, Sydney, NSW, Australia.

出版信息

Mult Scler Relat Disord. 2019 Feb;28:31-33. doi: 10.1016/j.msard.2018.12.004. Epub 2018 Dec 3.

Abstract

Secondary autoimmune disorders are a recognised complication of alemtuzumab treatment for multiple sclerosis. We report a case of autoimmune encephalitis manifesting as a polymorphic epilepsia partialis continua / status epilepticus seven months after the second course of alemtuzumab in a patient with previous autoimmune hypothyroidism and immune thrombocytopenic purpura. An MRI revealed multifocal cortical abnormalities and neuronal loss was evident on biopsy. Although testing for anti-neuronal antibodies was negative, the patient responded well to immunotherapy including plasma exchange. This is the first reported presentation of an autoimmune encephalopathy secondary to alemtuzumab therapy.

摘要

继发自身免疫性疾病是阿仑单抗治疗多发性硬化症的已知并发症。我们报告了一例自身免疫性脑炎病例,该患者曾患有自身免疫性甲状腺功能减退症和免疫性血小板减少性紫癜,在第二次阿仑单抗治疗后 7 个月出现局灶性持续部分性癫痫/癫痫持续状态。MRI 显示多灶性皮质异常,活检显示神经元丢失。尽管抗神经元抗体检测阴性,但患者对包括血浆置换在内的免疫治疗反应良好。这是首例报道的继发于阿仑单抗治疗的自身免疫性脑病。

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