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自身免疫性脑炎的感染触发因素:一例病例报告及文献综述

Infectious Trigger for Autoimmune Encephalitis: A Case Report and Literature Review.

作者信息

Sahar Najmus, Nurre Alexander Michael, Simon Ryan Q

机构信息

Wright State University Boonshoft School of Medicine, Miami Valley Hospital, Dayton, Ohio, USA.

Boonshaft School of Medicine, Class 2019, Dayton, Ohio, USA.

出版信息

Case Rep Infect Dis. 2019 Nov 6;2019:5731969. doi: 10.1155/2019/5731969. eCollection 2019.

Abstract

Herpes simplex virus 1 infection is a common cause of encephalitis (HSVE) in the United States. Post-HSVE development of N-methyl-D-aspartate receptor (NMDAR) antibodies resulting in autoimmune encephalitis is a rare complication, primarily affecting children and young adults. Anti-NMDAR develops 1-4 weeks after HSVE, manifesting as choreoathetosis and/or orofacial dyskinesia in children and psychiatric symptoms in young adults. We describe a case of a 61-year-old male who presented with agitation, behavioral changes, and confusion eight months after being treated for HSVE. Extensive investigation was unrevealing except for cerebrospinal fluid lymphocytic pleocytosis, a positive anti-NMDAR Ab titer 1 : 64, and imaging changes consistent with postviral encephalitis suggestive of HSV-induced anti-NMDAR encephalitis. Aggressive therapy resulted in limited success and persistent neurologic deficits. The unique features of this case are the old age of the patient and preceding HSVE which triggered this autoimmune process. Physicians should consider anti-NMDAR encephalitis in the differentials for relapsing patients after HSVE.

摘要

单纯疱疹病毒1型感染是美国脑炎(HSVE)的常见病因。HSVE后发生N-甲基-D-天冬氨酸受体(NMDAR)抗体导致自身免疫性脑炎是一种罕见的并发症,主要影响儿童和年轻人。抗NMDAR抗体在HSVE后1至4周出现,在儿童中表现为舞蹈手足徐动症和/或口面部运动障碍,在年轻人中表现为精神症状。我们描述了一例61岁男性病例,该患者在接受HSVE治疗八个月后出现躁动、行为改变和意识模糊。除脑脊液淋巴细胞增多、抗NMDAR抗体滴度为1:64阳性以及影像学改变符合病毒性脑炎后表现提示HSV诱导的抗NMDAR脑炎外,广泛检查未发现其他异常。积极治疗取得了有限的成功,患者仍存在持续性神经功能缺损。该病例的独特之处在于患者年龄较大且之前有HSVE引发了这一自身免疫过程。医生在HSVE后复发患者的鉴别诊断中应考虑抗NMDAR脑炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ba/6875379/af856015fd66/CRIID2019-5731969.001.jpg

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