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多发性梗死性痴呆的诊断。

Diagnosis of multi-infarct dementia.

作者信息

Erkinjuntii T, Sulkava R

机构信息

Department of Neurology, University of Helsinki, Finland.

出版信息

Alzheimer Dis Assoc Disord. 1991 Summer;5(2):112-21. doi: 10.1097/00002093-199100520-00008.

Abstract

Multi-infarct dementia (MID) is commonly considered a dementia syndrome evolving in connection with multiple ischemic brain lesions, without other changes known to cause dementia. The ischemic brain lesions result from various vascular mechanisms, and different brain mechanisms are involved in the genesis of MID. Typical features for MID are abrupt onset of cognitive symptoms, stepwise deterioration of mental functioning, and focal neurologic symptoms or signs, but in 20% of cases the onset is insidious and the course is even. The main steps in diagnosis of MID include diagnosis of dementia, diagnosis of specific causes of dementia and secondary factors potentially aggravating cognitive decline, and demonstration of ischemic brain changes assumed to be responsible for the evolution of dementia. Methods used for clinical diagnosis of MID include clinical history and examination, brain imaging, ischemic scores, neurophysiologic investigations, and a variety of laboratory investigations designed to detect concomitant illness. According to strict clinical criteria for MID, the accuracy of the antemortem diagnosis as verified postmortem in one series was approximately 90%.

摘要

多发性梗死性痴呆(MID)通常被认为是一种与多发性缺血性脑病变相关的痴呆综合征,不存在已知的其他导致痴呆的病变。缺血性脑病变由多种血管机制引起,不同的脑机制参与了MID的发病过程。MID的典型特征为认知症状突然发作、精神功能逐步衰退以及局灶性神经症状或体征,但在20%的病例中起病隐匿且病程平稳。MID诊断的主要步骤包括痴呆的诊断、痴呆特定病因及可能加重认知衰退的继发因素的诊断,以及证明假定为痴呆病情发展原因的缺血性脑改变。用于MID临床诊断的方法包括临床病史和检查、脑成像、缺血评分、神经生理学检查以及旨在检测伴发疾病的各种实验室检查。根据MID严格的临床标准,在一系列病例中经尸检证实的生前诊断准确率约为90%。

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