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与抗谷氨酸脱羧酶抗体相关的急性小脑共济失调,酷似米勒-费希尔综合征。

Acute Cerebellar Ataxia Associated with Anti-glutamic Acid Decarboxylase Antibodies Mimicking Miller Fisher Syndrome.

作者信息

Nakamura Yoshitsugu, Nakajima Hideto, Hosokawa Takafumi, Yamane Kazushi, Ishida Shimon, Kimura Fumiharu

机构信息

Division of Neurology, Department of Internal Medicine IV, Osaka Medical College, Japan.

出版信息

Intern Med. 2018 Jan 15;57(2):269-271. doi: 10.2169/internalmedicine.9190-17. Epub 2017 Nov 1.

Abstract

We herein report the case of a 53-year-old man with cerebellar ataxia with anti-glutamic acid decarboxylase antibody (GAD-Ab) who mimicked Miller Fisher syndrome (MFS). He developed ophthalmoplegia, diplopia, and gait ataxia for one week. The serum and cerebrospinal fluid GAD-Ab titers were greatly increased, and the GAD-Ab index suggesting intrathecal antibody synthesis was elevated, while GQ1b-Ab was negative. After steroid pulse therapy and following prednisolone, his symptoms dramatically improved over the course of 11 months with the simultaneous decline of GAD-Ab titers. This case indicates that cerebellar ataxia with GAD-Ab can present with acute neurological findings mimicking MFS, and that steroid therapy has an excellent therapeutic effect.

摘要

我们在此报告一例53岁患有抗谷氨酸脱羧酶抗体(GAD-Ab)相关性小脑共济失调的男性患者,其临床表现酷似米勒-费雪综合征(MFS)。他出现眼肌麻痹、复视和步态共济失调达一周时间。血清和脑脊液中GAD-Ab滴度大幅升高,提示鞘内抗体合成的GAD-Ab指数升高,而GQ1b-Ab为阴性。在接受类固醇冲击治疗及泼尼松龙治疗后,他的症状在11个月内显著改善,同时GAD-Ab滴度下降。该病例表明,GAD-Ab相关性小脑共济失调可表现出酷似MFS的急性神经学表现,且类固醇治疗具有极佳的治疗效果。

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本文引用的文献

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Guidelines for treatment of immune-mediated cerebellar ataxias.免疫介导性小脑共济失调的治疗指南。
Cerebellum Ataxias. 2015 Nov 10;2:14. doi: 10.1186/s40673-015-0034-y. eCollection 2015.
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Fisher syndrome.费希尔综合征。
Curr Treat Options Neurol. 2011 Feb;13(1):71-8. doi: 10.1007/s11940-010-0103-8.

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