Onofrj M, Fulgente T, Gambi D, Macchi G
Istituto di Neurologia, Università G. D'Annunzio, Chieti, Italy.
J Neurol. 1993 Jul;240(7):423-6. doi: 10.1007/BF00867355.
We describe the MRI changes preceding the onset of myoclonus in two patients whose post-mortem examination confirmed the diagnosis of Creutzfeldt-Jakob disease (CJD). MRI showed changes in the striatum early in the course of CJD (2-6 months after the onset of apathy, interpreted as depression, and 1-2 months before the onset of further clinical symptoms). Only in one patient did electroencephalography record the typical triphasic sharp-waves, 1 month after MRI.
我们描述了两名患者肌阵挛发作前的MRI变化,这两名患者的尸检确诊为克雅氏病(CJD)。MRI显示,在CJD病程早期(情感淡漠发作后2 - 6个月,被解释为抑郁,且在进一步临床症状发作前1 - 2个月)纹状体出现变化。仅一名患者在MRI检查1个月后,脑电图记录到典型的三相尖波。