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弥漫性路易体病。6例患者的神经病理学和生化研究。

Diffuse Lewy body disease. Neuropathological and biochemical studies of six patients.

作者信息

Dickson D W, Davies P, Mayeux R, Crystal H, Horoupian D S, Thompson A, Goldman J E

机构信息

Department of Pathology (Neuropathology), Rose F. Kennedy Center for Research in Mental Retardation and Human Development, Bronx, NY 10461.

出版信息

Acta Neuropathol. 1987;75(1):8-15. doi: 10.1007/BF00686786.

Abstract

Post-mortem pathological and biochemical studies are reported on six patients with progressive dementia. The characteristic pathological finding was neurofilament-containing cytoplasmic inclusions in cortical and subcortical neurons. The clinical and pathological findings were consistent with so-called diffuse Lewy body disease. The patients had variable changes of the Alzheimer type, with five of six patients displaying "plaques only" Alzheimer's changes. Biochemical studies showed profound decreases in neocortical choline acetyltransferase (ChAT) activities that correlated with marked neuronal loss in the basal nucleus of Meynert. ChAT activities were normal in the hippocampus in three patients who also had no significant Alzheimer type hippocampal changes. All patients had decreased cortical somatostatin-like immunoreactivity. Our observations suggest that dementia in diffuse Lewy body disease bears biochemical similarities to Alzheimer's disease, in that biochemical markers for both intrinsic cortical neurons and ascending cholinergic neurons are affected.

摘要

报告了6例进行性痴呆患者的尸检病理和生化研究结果。特征性病理发现为皮质和皮质下神经元中含有神经丝的胞质内包涵体。临床和病理表现与所谓的弥漫性路易体病一致。患者有阿尔茨海默病类型的不同变化,6例患者中有5例表现为“仅有斑块”的阿尔茨海默病变化。生化研究显示新皮质胆碱乙酰转移酶(ChAT)活性显著降低,这与Meynert基底核中明显的神经元丢失相关。3例海马ChAT活性正常的患者海马也无明显的阿尔茨海默病类型变化。所有患者皮质生长抑素样免疫反应性均降低。我们的观察结果表明,弥漫性路易体病中的痴呆在生化方面与阿尔茨海默病相似,因为内在皮质神经元和上行胆碱能神经元的生化标志物均受到影响。

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