Enomoto M, Mizutani T, Takasaki M, Yamada S, Sakata M
Department of Neuropathology, Tokyo Metropolitan Institute of Gerontology.
Nihon Ronen Igakkai Zasshi. 1998 May;35(5):374-81. doi: 10.3143/geriatrics.35.374.
We investigated seven brains from patients 99-105 years of age with a clinical diagnosis of Alzheimer-type dementia (ATD). The pathological findings were as follows. 1) These cases could be divided into two groups: cases with localized cortical atrophy in the medial part of the temporal lobe, and a case with diffuse atrophy in the cerebral cortex. Atrophied cortex in both groups showed laminar degeneration consisting of neuronal loss, neuropil loosening and astrocytosis resulting in fibrillary gliosis, which was particularly marked in the 2nd and 3rd layers of the cerebral cortex. In contrast, the structure of the six cortical layers was preserved when there was no laminar degeneration. Laminar degeneration correlated with cortical atrophy. 2) Cases with localized atrophy were further divided into two groups: group 1 (4 cases) showed small numbers of senile plaques (SPs) and large numbers of neurofibrillary tangles (NFTs' in CA1 of the hippocamupus, subiculum, and parahippohcampul gyrus, while group 2 (2 cases) showed widespread and numerous SPs and NFTs in the cerebral cortex. The distribution of SPs and NFTs in group 2 was similar to that of the case (group 3) with diffuse cortical atrophy. It was considered that group 2 was limbic type ATD and that group 3 was neocortical type ATD, because both groups met our pathological diagnostic criteria ATD. In contrast, group 1 could not be regarded as ATD because the numbers of SPs and NFTs were below those found in ATD, even though this group showed laminar degeneration the same as that of groups 2 and 3. It therefore is likely that group 1 is a unique type of degenerative dementia, pathogenetically different from ATD.
我们研究了7例年龄在99至105岁之间、临床诊断为阿尔茨海默型痴呆(ATD)患者的大脑。病理结果如下:1)这些病例可分为两组:颞叶内侧局部皮质萎缩的病例,以及大脑皮质弥漫性萎缩的1例。两组萎缩的皮质均显示层状变性,包括神经元丢失、神经纤维疏松和星形细胞增多,导致纤维性胶质增生,在大脑皮质第2层和第3层尤为明显。相比之下,无层状变性时,六层皮质结构保持完整。层状变性与皮质萎缩相关。2)局部萎缩的病例进一步分为两组:第1组(4例)在海马CA1区、下托和海马旁回显示少量老年斑(SPs)和大量神经原纤维缠结(NFTs),而第2组(2例)在大脑皮质显示广泛且大量的SPs和NFTs。第2组中SPs和NFTs的分布与皮质弥漫性萎缩的病例(第3组)相似。由于两组均符合我们的ATD病理诊断标准,因此认为第2组为边缘型ATD,第3组为新皮质型ATD。相比之下,第1组不能被视为ATD,因为尽管该组显示与第2组和第3组相同的层状变性,但其SPs和NFTs的数量低于ATD中的发现。因此,第1组很可能是一种独特类型的退行性痴呆,在发病机制上与ATD不同。