Misumi Misumi, Nishida Yasuto, Araki Shukuro
Department of Neurology, Omuta Tenryo Hospital.
Rinsho Shinkeigaku. 2006 Apr;46(4):291-3.
A 59-year-old woman with Gerstmann-Sträussler-Scheinker syndrome (GSS P102L) was reported. She slowly developed progressive gait disturbance and limb ataxia by the age of 58, subsequently followed by dementia and myoclonus. EEG showed periodic synchronous discharges, and MRI by diffusion weighted imaging revealed abnormal high signal intensity lesions in the bilateral cerebral cortex and basal ganglia. A prorin-for-leution substitution at codon 102 of the prion protein gene was demonstrated; and thus, she was diagnosed as GSS (P102L). This is a case of GSS presenting high intensity lesions in the cerebral cortex on diffusion weighted MRI; it suggests that MRI findings disease stages in GSS.
报道了一名59岁患有格斯特曼-施特劳斯勒-谢inker综合征(GSS P102L)的女性。她在58岁时逐渐出现进行性步态障碍和肢体共济失调,随后出现痴呆和肌阵挛。脑电图显示周期性同步放电,磁共振成像(MRI)弥散加权成像显示双侧大脑皮质和基底神经节有异常高信号强度病变。在朊蛋白基因的第102密码子处证实存在脯氨酸-亮氨酸替代;因此,她被诊断为GSS(P102L)。这是一例在弥散加权MRI上大脑皮质出现高强度病变的GSS病例;提示MRI表现可反映GSS的疾病阶段。