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以运动性震颤和小脑共济失调为初发表现的菊池-藤本病

Kinetic tremor and cerebellar ataxia as initial manifestations of Kikuchi-Fujimoto's disease.

作者信息

Moon Ju-Sun, Il Kim Gwang, Koo Young-Ho, Kim Hyun-Sook, Kim Won-Chan, Kim Ok-Joon, Oh Seung-Hun

机构信息

Department of Neurology, Pochon CHA University college of medicine, South Korea.

出版信息

J Neurol Sci. 2009 Feb 15;277(1-2):181-3. doi: 10.1016/j.jns.2008.10.021. Epub 2008 Nov 22.

Abstract

Involvement of central nervous system occasionally occurs as a form of aseptic meningitis in Kikuchi-Fujimoto disease (KFD). However, acute cerebellar symptoms are very rare in KFD. We describe a 42 year-old woman presenting kinetic tremor and gait ataxia preceding cervical lymphadenopathy. The diagnosis of KFD was made based on pathology. Lymphocyte-dominant pleocytosis was observed in cerebrospinal fluid. Brain and spinal magnetic resonance imaging showed no structural abnormalities. Acute cerebellar symptoms and cervical lymphadenopathy disappeared spontaneously within 2 months. This case of KFD involved unusual acute cerebellar symptoms. Selective involvement of the cerebellar system by viral or immunologic response may be attributed to acute cerebellar symptoms in KFD.

摘要

中枢神经系统受累在菊池-藤本病(KFD)中偶尔以无菌性脑膜炎的形式出现。然而,KFD中急性小脑症状非常罕见。我们描述了一名42岁女性,在颈部淋巴结病之前出现运动性震颤和步态共济失调。KFD的诊断基于病理学。脑脊液中观察到以淋巴细胞为主的细胞增多。脑和脊髓磁共振成像未显示结构异常。急性小脑症状和颈部淋巴结病在2个月内自发消失。该例KFD伴有不寻常的急性小脑症状。病毒或免疫反应对小脑系统的选择性累及可能是KFD中急性小脑症状的原因。

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