Shibayama H, Kobayashi H, Nakagawa M, Yamada K, Iwata H, Iwai K, Takeuchi T, Mu-Qune X, Ishihara R, Iwase S
Department of Psychiatry, Nagoya University School of Medicine, Japan.
Clin Neuropathol. 1992 Sep-Oct;11(5):237-50.
Five patients with non-Alzheimer non-Pick dementia combined with Fahr's syndrome were studied. Atypical clinical pictures emerged from an evaluation of these cases. Their symptoms and signs could be attributed neither to Alzheimer's disease nor to Pick's disease but to a partial mixture of both. The neuropathological changes were characteristic, and the common findings were as follows: 1) the absence of senile (neuritic) plaques, 2) the widespread presence of numerous neurofibrillary tangles throughout the neocortex, 3) a calcareous deposition of Fahr's type, 4) a circumscribed cerebral atrophy in the temporal or/and frontal lobes, 5) a moderate or severe demyelination and fibrous gliosis in the white matter of the atrophied areas and 6) a mild or moderate neuronal loss in the nucleus basalis of Meynert. These neuropathological changes were not due to Alzheimer's disease nor to Pick's disease. Similar cases reported previously were reviewed.
对5例非阿尔茨海默病非皮克病合并法尔综合征的患者进行了研究。对这些病例的评估呈现出非典型的临床症状。其症状和体征既不能归因于阿尔茨海默病,也不能归因于皮克病,而是两者的部分混合。神经病理学改变具有特征性,常见表现如下:1)无老年(神经炎性)斑块;2)整个新皮质广泛存在大量神经原纤维缠结;3)法尔型钙质沉积;4)颞叶或/和额叶局限性脑萎缩;5)萎缩区域白质中度或重度脱髓鞘及纤维性胶质增生;6)迈内特基底核轻度或中度神经元丢失。这些神经病理学改变并非由阿尔茨海默病或皮克病所致。对先前报道的类似病例进行了回顾。