Mizutani T, Amano N, Sasaki H, Morimatsu Y, Mori H, Yoshimura M, Yamanouchi H, Hayakawa K, Shimada H
Department of Neuropathology, Tokyo Metropolitan Institute of Gerontology, Japan.
Acta Neuropathol. 1990;80(6):575-80. doi: 10.1007/BF00307623.
Seven cases of senile dementia of Alzheimer type (SDAT) with unusual clinico-pathological findings are reported. The patients showed neuronal loss in laminar pattern, with gliosis exclusively confined to the CA1 of the hippocampus, the area of the hippocampal gyrus (entorhinal cortex) and medial occipitotemporal cortex. This change was more pronounced in the oral region. The subcortical white matter showed more pronounced fibrillary gliosis than loss of myelin. Both Alzheimer's neurofibrillary tangles and senile plaques were less marked than those usually seen in SDAT. The mental disturbance started after the age of 65 in all patients. The main clinical feature was marked character change in addition to disturbance of cognitive function. Cranial computed tomography showed marked dilatation of the oral portion of the inferior horn of the lateral ventricle in the early stage. It was apparent that although the cases in this group could be incorporated within in the spectrum of SDAT, they could also be considered to represent a variant of SDAT. This group could contribute to an understanding of the clinico-pathological spectrum of SDAT as well as indicating ways of managing such patients.
报告了7例具有不寻常临床病理表现的阿尔茨海默病型老年痴呆(SDAT)。患者表现为层状神经元丢失,胶质增生仅局限于海马体的CA1区、海马回(内嗅皮质)区域及枕颞内侧皮质。这种变化在口部区域更为明显。皮质下白质的纤维性胶质增生比髓鞘脱失更明显。阿尔茨海默神经原纤维缠结和老年斑均不如SDAT中常见的那样明显。所有患者的精神障碍均始于65岁之后。除认知功能障碍外,主要临床特征为显著的性格改变。头颅计算机断层扫描显示早期外侧脑室下角口部明显扩张。显然,尽管该组病例可归入SDAT范围,但也可认为代表了SDAT的一种变体。该组病例有助于理解SDAT的临床病理谱,并为这类患者的治疗提供思路。