Muramoto T, Kitamoto T, Koga H, Tateishi J
Department of Neuropathology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Acta Neuropathol. 1992;84(6):686-9. doi: 10.1007/BF00227747.
We report here a 75-year-old-male with a slowly progressive dementia of 5-year duration along with a rapid exacerbation of symptoms in the terminal 3 months. Neuropathological examinations revealed findings consistent with conspicuous Alzheimer's disease and mild Creutzfeldt-Jakob disease (CJD). The plaque amyloid was exclusively composed of beta-protein. The immunohistochemistry of prion protein using hydrolytic autoclaving pretreatment showed diffuse gray matter stainings in the sections of both the cerebral and cerebellar cortices. This method was thus considered useful in confirming the diagnosis of CJD for this case.
我们在此报告一名75岁男性,患有持续5年的缓慢进展性痴呆,并在最后3个月症状迅速加重。神经病理学检查发现与明显的阿尔茨海默病和轻度克雅氏病(CJD)相符的结果。斑块淀粉样蛋白仅由β蛋白组成。使用水解高压灭菌预处理的朊病毒蛋白免疫组织化学显示大脑和小脑皮质切片中均有弥漫性灰质染色。因此,该方法被认为有助于确诊该病例的CJD。