Autoimmune encephalitis presenting with atypical parkinsonism: A case report and review of the literature

IF 0.4 Q4 CLINICAL NEUROLOGY
Yoya Ono, K. Higashida, A. Takekoshi, A. Kimura, T. Shimohata
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引用次数: 0

Abstract

An 81‐year‐old man developed axial rigidity, bradykinesia, and cognitive impairment within 6 weeks. On initial examination, he was misdiagnosed with progressive supranuclear palsy (PSP). Brain magnetic resonance imaging showed hyperintensities in the bilateral mesial temporal lobes and basal ganglia. Neuronal antibodies previously reported in autoimmune encephalitis mimicking PSP were negative. Immunohistochemical and immunocytochemical analysis revealed the autoantibodies recognized neuronal surface and intracellular antigens. The diagnostic criteria for probable autoimmune encephalitis were fulfilled. We diagnosed him with autoimmune encephalitis. Intravenous immunoglobulin and steroid therapy improved his symptoms. The presence of novel autoantibodies causing autoimmune encephalitis presenting with atypical parkinsonism was suggested.
以非典型帕金森病为表现的自身免疫性脑炎:1例报告及文献复习
一例81岁男性患者在6周内出现轴向僵硬、运动迟缓和认知障碍。在初步检查时,他被误诊为进行性核上性麻痹(PSP)。脑磁共振成像显示双侧内侧颞叶和基底神经节高信号。先前报道的模拟PSP的自身免疫性脑炎的神经元抗体为阴性。免疫组织化学和免疫细胞化学分析显示自身抗体识别神经元表面和细胞内抗原。符合可能为自身免疫性脑炎的诊断标准。我们诊断他患有自身免疫性脑炎静脉注射免疫球蛋白和类固醇治疗改善了他的症状。存在新的自身抗体引起自身免疫性脑炎表现为不典型帕金森病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
76
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