Mizutani T, Okumura A, Oda M, Shiraki H
J Neurol Neurosurg Psychiatry. 1981 Feb;44(2):103-15. doi: 10.1136/jnnp.44.2.103.
Eight necropsy cases of a "panencephalopathic" type of Creutzfeldt-Jakob disease (CJD) in the Japanese are reported. The reasons why this type should be discussed separately from other types of CJD are that there is primary involvement of the cerebral white matter as well as the cerebral cortex, and that the white matter lesion of one Japanese human brain with CJD similar to the present group has been successfully transmitted to experimental animals.
本文报告了8例日本“全脑病变型”克雅氏病(CJD)的尸检病例。之所以要将此类型与其他类型的CJD分开讨论,原因在于脑白质以及大脑皮层均有原发性病变,并且1例与本研究组类似的患CJD的日本人脑白质病变已成功传播给实验动物。