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以孤立性失语为表现的克雅氏病

Creutzfeldt-Jakob disease presenting as isolated aphasia.

作者信息

Mandell A M, Alexander M P, Carpenter S

机构信息

Medical Service, Edith Nourse Rogers Memorial VA Medical Center, Bedford, MA 01730.

出版信息

Neurology. 1989 Jan;39(1):55-8. doi: 10.1212/wnl.39.1.55.

Abstract

Progressive aphasia without dementia (primary progressive aphasia) is increasingly recognized as an important neurobehavioral syndrome. Clinical diagnosis of progressive aphasia is difficult early in its course, and the differential diagnosis is usually said to include Alzheimer's and Pick's diseases. We report a 61-year-old man with autopsy-proven Creutzfeldt-Jakob disease (CJD) whose major initial manifestation was a progressive, fluent aphasia. Myoclonus was absent, and characteristic EEG abnormalities appeared relatively late. We believe that this case of CJD is unique in its presentation of profound and isolated aphasia. CJD should be considered in the differential diagnosis of the progressive aphasia syndrome.

摘要

无痴呆的进行性失语(原发性进行性失语)日益被视为一种重要的神经行为综合征。进行性失语在病程早期临床诊断困难,通常认为鉴别诊断包括阿尔茨海默病和匹克病。我们报告一名61岁男性,经尸检证实患有克雅氏病(CJD),其主要初始表现为进行性、流利性失语。无肌阵挛,特征性脑电图异常出现相对较晚。我们认为该例CJD在呈现严重且孤立的失语方面具有独特性。在进行性失语综合征的鉴别诊断中应考虑CJD。

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