Nedz'ved' M K, Protas I I, Lystsova E G, Guzov S A, Mil'kamanovich E K
Arkh Patol. 1985;47(12):14-20.
The analysis of 7 cases of subacute spongiform encephalopathy, the Creutzfeldt-Jacob disease (CJD), is given. Three main morphological features are typical for this disease: spongiform change of the grey matter, progressive neuronal loss and proliferation of the astroglia cells. Unlike the other spongiform conditions, spongiform change in the CJD develops in neuropile of the brain grey matter. As a rule, the disease affects at first the cortex of the cerebral hemispheres, then subcortical nuclear groups, cerebellum and more rarely nuclear groups of the brain stem. The demyelinization of the white matter of the cerebral hemispheres is not obligatory for the CJD and appears in cases with a severe lesion of the grey matter.
本文对7例亚急性海绵状脑病即克雅氏病(CJD)进行了分析。该疾病具有三个主要形态学特征:灰质海绵状改变、进行性神经元丢失以及星形胶质细胞增生。与其他海绵状病变不同,CJD的海绵状改变发生在脑灰质的神经毡中。通常,该疾病首先影响大脑半球皮质,然后是皮质下核团、小脑,很少累及脑干核团。大脑半球白质脱髓鞘并非CJD所必需,而是出现在灰质严重受损的病例中。