Ishino H, Sasaki T, Yamashita K, Senô H, Kodaka H, Yoshinaga J, Ideshita H, Yamanaka T, Hikiji A
Clin Neuropathol. 1987 Mar-Apr;6(2):61-6.
An autopsy case of progressive supranuclear palsy with onset at age 53 and a clinical course of 7 years is reported. The clinico-pathological characteristics of the case were as follows: Fibrillary gliosis of the midbrain and pontine reticular formation corresponded clinically to personality changes: The patient had formerly been irascible and became extremely mild-mannered. He showed lack of spontaneity and initiative and slowing of thought processes, taking him longer than normal to find words and ideas. Gliosis of the nucleus ventralis lateralis of the thalamus was secondary to the degeneration of the cerebellar dentate nucleus and the globus pallidus from which they receive fibers. Neurofibrillary tangles were found in the cerebral cortex.
报告了一例53岁起病、病程7年的进行性核上性麻痹尸检病例。该病例的临床病理特征如下:中脑和脑桥网状结构的纤维性胶质增生在临床上与人格改变相对应:患者以前脾气暴躁,后来变得极为温和。他表现出缺乏自发性和主动性,思维过程迟缓,找词和想法的时间比正常情况要长。丘脑腹外侧核的胶质增生继发于小脑齿状核和苍白球的变性,丘脑腹外侧核从它们接收纤维。在大脑皮层发现了神经原纤维缠结。