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A Case of Atypical Alcoholic Cerebellar Ataxia Yasushi MORIYAMA 1 , Masaru MIMURA 2 , Motoichiro KATO 3 , Aihide YOSHINO 4 , Jyun TAKAHASHI 5 , Tsunekatsu HARA 1 , Haruo KASHIMA 6 1Komagino Hospital 2Department of Neuropsychiatry, Showa University School of Medicine 3Department of Neuropsychiatry, Tokyo Dental College Ichikawa General Hospital 4Department of Psychiatry, National Defense Medical College 5Department of Neurology, National Center of Neurology and Psychiatry, Musashi Hospital 6Department of Neuropsychiatry, Keio University School of Medicine Keyword: Alcoholism , Cerebellar degeneration , Ataxia , TRH treatment pp.1345-1350
Published Date 2001/12/15
DOI https://doi.org/10.11477/mf.1405902548
  • Abstract
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 We report the case of a patient with chronic alcoholism who presented with progressive cerebellar ataxia despite complete abstinence. Our patient was remarkably different from the cases with alcoholic cerebellar degeneration described by Victor et al. (1959), in that his cerebellar ataxia progressed for seven months after he began to abstain from alcohol. The clinical features were also characteristic in that ataxia involved his upper limbs and eye movements as well as speech. The ataxia ceased deteriorating after TRH administration. A brain CT had already demonstrated cerebellar atrophy even before the onset of ataxia, but this atrophy, revealed no significant interval change in the frequency of ataxic movements.


Copyright © 2001, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-126X 印刷版ISSN 0488-1281 医学書院

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