Morice J, Turpin J C, Pluot M, Level G
Rev Neurol (Paris). 1975 Aug;131(8):573-82.
The authors describe a case of sub-acute spongiform encephalopathy with an ultrastructural study in a man of 65 with associated dementia, extra-pyramidal syndrome, myoclonia, optical disorders, pyramidal syndrome and speech disorders, rapidly leading to death one and a half months later. Electroencephalograms were at first disorganized with persistent delta and theta activity and only in the last record did short runs of repetitive activity appear. Histologically, there was severe status spongiosus, a moderate degree of neuronal depopulation with a noticeable astrocytary gliosis. Under the electron microscope, the neuropile in the astrocytes was found to be pitted with numerous cavities and so were, to a lesser extent, the axonal projections. The vessels were normal. Nothing was found to indicate viral structures. Attention is drawn to the nosological connection between this type of observation and Creutzfeldt-Jakob disease.
作者描述了一例亚急性海绵状脑病病例,并对一名65岁男性进行了超微结构研究。该患者伴有痴呆、锥体外系综合征、肌阵挛、视力障碍、锥体综合征和言语障碍,一个半月后迅速死亡。脑电图最初表现为紊乱,伴有持续的δ波和θ波活动,仅在最后一次记录中出现了短暂的重复性活动。组织学上,存在严重的海绵状状态、中度神经元减少以及明显的星形细胞胶质增生。在电子显微镜下,发现星形胶质细胞中的神经纤维网有许多凹陷,轴突投射也有程度较轻的类似情况。血管正常。未发现表明病毒结构的迹象。提请注意这类观察结果与克雅氏病之间的疾病分类学联系。