Scheltens P, Ravid R, Kamphorst W
Department of Neurology, Free University Hospital, Amsterdam, The Netherlands.
Neurology. 1994 Feb;44(2):279-82. doi: 10.1212/wnl.44.2.279.
We report the histopathologic and immunohistochemical findings of a patient who suffered from primary progressive aphasia for 13 years. During the course of his illness, he was diagnosed as having Pick's disease, based on gradually progressive mild personality changes and MRI findings of severe bilateral temporal lobe atrophy. There was severe neuronal loss in the temporal gyri, intense gliosis throughout the cortex, and mild gliosis of the temporal white matter, without any changes typical for Alzheimer's disease or Pick's disease. Using the antibody Alz-50, we found many Alz-50-positive neurons that exhibited a granular or diffuse cytoplasmic stain without fibrous structures in the temporal and parietal cortex, but no ubiquitin or beta (A4) protein-reactive cells, nor spongiform changes. Staining for Alz-50 and ubiquitin did not reveal the presence of Pick bodies or Lewy bodies. We consider this case to be an example of nonspecific cortical degeneration. Our findings stress the need for histopathologic verification of the primary progressive aphasia syndrome.
我们报告了一位患有原发性进行性失语症13年患者的组织病理学和免疫组化结果。在其病程中,基于逐渐进展的轻度人格改变以及严重双侧颞叶萎缩的MRI表现,他被诊断为患有皮克病。颞回存在严重的神经元丧失,整个皮质有明显的胶质增生,颞叶白质有轻度胶质增生,无阿尔茨海默病或皮克病的典型改变。使用Alz - 50抗体,我们在颞叶和顶叶皮质发现许多Alz - 50阳性神经元,其呈现颗粒状或弥漫性细胞质染色,无纤维结构,但未发现泛素或β(A4)蛋白反应性细胞,也无海绵状改变。Alz - 50和泛素染色未显示皮克小体或路易小体的存在。我们认为该病例是非特异性皮质变性的一个例子。我们的发现强调了对原发性进行性失语症综合征进行组织病理学验证的必要性。