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以小脑性共济失调为首发症状且小脑受累的抗NMDAR脑炎患者:1例罕见病例报告及文献复习

Cerebellar ataxia as the initial symptom with lesions involving the cerebellum in patient with anti-NMDAR encephalitis: A rare case report and literature review.

作者信息

Wang Baojie, Wang Chunjuan, Ren Haitao, Guan Hongzhi, Guo Shougang

机构信息

Shandong Provincial ENT Hospital, Shandong Provincial ENT Hospital Affiliated to Shandong University, Jinan, Shandong, China.

Shandong Provincial Hospital affiliated to Shandong University, Jinan, Shandong, China.

出版信息

J Neuroimmunol. 2020 Sep 15;346:577293. doi: 10.1016/j.jneuroim.2020.577293. Epub 2020 Jun 17.

Abstract

Cerebellar ataxia is an atypical presentation of anti-N-methyl-d-aspartate receptor (anti-NMDAR) encephalitis. In patients with anti-NMDAR encephalitis, cerebellar ataxia often develops simultaneously or sequentially with clinical features of demyelinating disorders, paraneoplastic neurologic syndromes, despite unremarkable brain magnetic resonance imagerying (MRI) findings. Herein, we report a patient with anti-NMDAR encephalitis who developed dizziness and gait ataxia as the initial symptoms, simultaneously showing MRI hyperintensities involving the cerebellum, even before manifesting behavioral and cognitive symptoms. We excluded the co-occurrence of other autoantibodies using cell- and tissue-based assays to establish a confirmed diagnosis of definite anti-NMDAR encephalitis.

摘要

小脑性共济失调是抗 N-甲基-D-天冬氨酸受体(抗 NMDAR)脑炎的一种非典型表现。在抗 NMDAR 脑炎患者中,尽管脑部磁共振成像(MRI)检查结果无明显异常,但小脑性共济失调常与脱髓鞘疾病、副肿瘤性神经综合征的临床特征同时或相继出现。在此,我们报告 1 例抗 NMDAR 脑炎患者,其最初症状为头晕和步态共济失调,甚至在出现行为和认知症状之前,小脑就已出现 MRI 高信号。我们通过基于细胞和组织的检测方法排除了其他自身抗体的共存,从而确诊为明确的抗 NMDAR 脑炎。

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