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阿尔茨海默病的路易体变异型。临床及病理发现。

The Lewy-body variant of Alzheimer's disease. Clinical and pathological findings.

作者信息

Förstl H, Burns A, Luthert P, Cairns N, Levy R

机构信息

Institute of Psychiatry, London.

出版信息

Br J Psychiatry. 1993 Mar;162:385-92. doi: 10.1192/bjp.162.3.385.

Abstract

At post-mortem, Lewy bodies (LBs) were found in the brainstem and neocortex of eight out of 65 patients who had been collected during a prospective long-term study on clinically diagnosed Alzheimer's disease. All eight patients had accompanying Alzheimer pathology which was less severe than in a sample of eight age- and sex-matched patients from the same study with neuropathologically verified Alzheimer's disease. Parkinsonian features were more common in patients with LBs. There were no particular differences in duration of illness, severity of cognitive impairment, presence of hallucinations, or fluctuations in the course of illness. Frontal cerebral atrophy was more marked in patients with LBs, as was the loss of neurons in the basal nucleus of Meynert and the substantia nigra. Cognitive performance correlated with the number of pigmented neurons in the substantia nigra. We conclude that the differential diagnosis of LB dementia should be considered in patients satisfying NINCDS-ADRDA criteria for Alzheimer-type dementia who show marked Parkinsonian features and a frontal accentuation of cerebral atrophy.

摘要

在尸检时,在一项对临床诊断为阿尔茨海默病的前瞻性长期研究中收集的65例患者中的8例患者的脑干和新皮质中发现了路易小体(LB)。所有8例患者均伴有阿尔茨海默病病理改变,但其严重程度低于来自同一研究的8例年龄和性别匹配且经神经病理学证实为阿尔茨海默病的患者样本。帕金森特征在有路易小体的患者中更为常见。在疾病持续时间、认知障碍严重程度、幻觉的存在或病程波动方面没有特别差异。额叶脑萎缩在有路易小体的患者中更为明显,Meynert基底核和黑质中的神经元丢失也是如此。认知表现与黑质中色素沉着神经元的数量相关。我们得出结论,对于符合NINCDS-ADRDA标准的阿尔茨海默型痴呆患者,若表现出明显的帕金森特征和额叶脑萎缩加重,应考虑路易小体痴呆的鉴别诊断。

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