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50例克雅氏病的小脑改变,重点关注颗粒细胞萎缩变异型。

Cerebellar changes in 50 cases of Creutzfeldt-Jakob disease with emphasis on granule cell atrophy variant.

作者信息

Hauw J J, Gray F, Baudrimont M, Escourolle R

出版信息

Acta Neuropathol Suppl. 1981;7:196-8. doi: 10.1007/978-3-642-81553-9_59.

Abstract

Cerebellar changes have been found in 41/50 cases of Creutzfeldt-Jakob disease. They were severe in 9 cases. We did not find significant correlation between the cerebellar symptoms and signs pointed out in clinical records and prominent cerebellar changes. The only exception consisted in dentate nucleus involvement which was more frequently related to those symptoms and signs. 5 of the cases with severe changes were characterized by predominant granule cell atrophy without kuru plaques. The mean age of death (56.0) was significantly lower in this variant than that of patients with other cerebellar changes (64.4) (p less than 0.01). The granule cell atrophy seems a distinct variant on the basis of age of death and pathological changes. However, it is not characterized by the presence of kuru plaques.

摘要

在50例克雅氏病患者中,有41例发现小脑病变。其中9例病变严重。我们未发现临床记录中指出的小脑症状和体征与明显的小脑病变之间存在显著相关性。唯一的例外是齿状核受累,它与那些症状和体征的相关性更高。5例病变严重的病例以颗粒细胞萎缩为主,无库鲁斑。此变异型患者的平均死亡年龄(56.0岁)显著低于其他小脑病变患者(64.4岁)(p<0.01)。基于死亡年龄和病理变化,颗粒细胞萎缩似乎是一种独特的变异型。然而,它的特征不是存在库鲁斑。

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