类固醇反应性帕金森症和脑病:病例报告

Toluwalase Oluwakemi Tofade, G. K. Harrold, Arjun Laud, A. Wills, N. Venna
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摘要

我们描述了一名出现快速进展性帕金森病和脑病的患者,该患者被诊断为血清阴性自身免疫性脑炎(AE)。以亚急性帕金森病作为血清阴性自身免疫性脑炎的一种表现形式并不常见,仅有少数类似病例发表在文献中。一名 71 岁的男子出现了严重的流感样症状,认知能力迅速下降,检查发现其具有帕金森病特征。最初的脑磁共振成像(MRI)并无异常,但脑脊液(CSF)分析显示有淋巴细胞增多和蛋白水平升高。对神经抗体和感染性病原体的彻底检查均呈阴性。他的症状最初有所波动,但在开始使用泼尼松的几天内明显好转,而在泼尼松减量后又急剧恶化。服用泼尼松后,他的脑脊液多细胞症也有所好转。恢复使用泼尼松后,复发症状再次缓解。自身免疫性神经病学的研究范围在不断发展,医生应了解自身免疫性脑炎的临床表现多种多样。我们旨在强调,对于出现急性或亚急性帕金森病的患者,排除自身免疫性脑炎的重要性。本病例还进一步说明,抗体检测阴性并不能排除自身免疫性脑炎的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Steroid- Responsive Parkinsonism and Encephalopathy: A Case Report
We describe a patient who presented with rapidly progressive parkinsonism and encephalopathy and was diagnosed with seronegative autoimmune encephalitis (AE). Subacute parkinsonism as a manifestation of seronegative AE is uncommon with only a handful of similar cases published in literature. A 71-year-old man presented with severe flu like symptoms, rapidly progressive cognitive decline and was found to have parkinsonian features on examination. Initial brain magnetic resonance imaging (MRI) was unremarkable however, cerebrospinal fluid (CSF) analysis revealed a lymphocytic pleocytosis and elevated protein level. Thorough searches for neural antibodies and infectious pathogens were negative. His symptoms fluctuated initially but markedly improved within days of starting prednisone and dramatically worsened after prednisone was tapered off. His CSF pleocytosis also improved on prednisone. Relapses again resolved with resumption of prednisone. The scope of autoimmune neurology Is constantly evolving, and physicians should be aware of the diverse and heterogenous clinical presentations of autoimmune encephalitis. We aim to emphasize the importance of ruling out autoimmune encephalitis in patients presenting with acute or subacute parkinsonism. This case additionally reinforces that negative antibody tests do not exclude the diagnosis of AE.
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