Agostini L, Bernardi G, Giacomini P
Riv Neurol. 1978 May-Jun;48(3):271-83.
A case of Progressive Supranuclear Palsy (The Steele-Richardson-Olszewski Syndrome) is presented. The chief clinical features are described. The neuropathological investigation confirmed the clinical diagnosis showing neuronal depopulation, gliosis and neurofibrillary degeneration with the characteristic topography in the brain stem, cerebellum and the subthalamic nuclei. They conclude with the hypothesis that sometimes a pregress cranial trauma can have an important role in the onset of this disease.
本文报告一例进行性核上性麻痹（斯蒂尔-理查森-奥尔谢夫斯基综合征）。描述了主要临床特征。神经病理学检查证实了临床诊断，显示神经元减少、胶质细胞增生和神经原纤维变性，其特征性分布于脑干、小脑和丘脑底核。他们最后提出一种假说，即有时既往的颅脑外伤在该疾病的发病中可能起重要作用。
