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格斯特曼-施特劳斯勒-谢inker病。脑活检的电子显微镜观察

Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsy.

作者信息

Schlote W, Boellaard J W, Schumm F, Stöhr M

出版信息

Acta Neuropathol. 1980;52(3):203-11. doi: 10.1007/BF00705808.

Abstract

Light and electron microscopic observations are reported on a brain biopsy of a man of 59 with a rare familial disease of the CNS and a 5-year clinical course. Electron micrographs of the frontal biopsy reveal plaque-like deposits composed of amyloid cores, often multicentric in the cortex and subcortical white matter. They are localized between enlarged astrocytic processes. In the neuropil they are sometimes associated with abnormal neuritic processes, in the white matter with processes of fibrous astroglia and basement membranes. There are no signs of primary neuritic or synaptic involvement in the plaque formation which is more obviously associated with altered astrocytic processes. Moreover, degenerative alterations in the cortical vessels and slight astroglial spongiform changes as well as oligodendroglial proliferation can be found. Plaques are considered to be mainly of the kuru type; the relationship with transmissible spongiform encephalopathies is discussed.

摘要

本文报告了对一名59岁男性进行脑活检的光镜和电镜观察结果,该患者患有罕见的中枢神经系统家族性疾病,临床病程为5年。额叶活检的电子显微镜照片显示,斑块样沉积物由淀粉样核心组成,在皮质和皮质下白质中常为多中心分布。它们位于增大的星形胶质细胞突起之间。在神经纤维网中,它们有时与异常的神经突过程相关,在白质中与纤维性星形胶质细胞和基底膜的过程相关。在斑块形成过程中没有原发性神经突或突触受累的迹象,斑块形成更明显地与星形胶质细胞过程改变有关。此外,还可发现皮质血管的退行性改变、轻微的星形胶质细胞海绵状改变以及少突胶质细胞增生。斑块主要被认为是库鲁病类型;并讨论了其与传染性海绵状脑病的关系。

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