Martínez Barros M, Ramos Peek J, Vega R, Escobar A
Departamento de Electrofisiologia Clínica, UNAM, México DF.
Gac Med Mex. 1995 Sep-Dec;131(5-6):591-6.
Creutzfeldt-Jakob disease (CJD) is one of a small group of the so-called spongiform encephalopathies. It is a rare transmissible disorder which is characterized by progressive and irreversible neurological damage. There are few reports where clinical manifestations are correlated with neurophysiologic and histopathologic findings. The present paper includes three cases of CJD where alterations in evoked potentials and brain mapping studies gave valuable information, especially in those where the clinical picture and the electroencephalogram were non-specific, we conclude that these alterations suggest that the classic histopathological changes in C-J disease involves both cortical and subcortical structures.
克雅氏病(CJD)是少数几种所谓的海绵状脑病之一。它是一种罕见的可传播疾病,其特征是进行性和不可逆的神经损伤。很少有关于临床表现与神经生理学和组织病理学发现相关的报道。本文包括3例克雅氏病病例,其中诱发电位和脑图谱研究的改变提供了有价值的信息,特别是在那些临床表现和脑电图无特异性的病例中。我们得出结论,这些改变表明克雅氏病的经典组织病理学变化涉及皮质和皮质下结构。