Dementia with Lewy bodies.

Bailliere's clinical neurology Pub Date : 1997-04-01
G G Lennox, J S Lowe
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Abstract

Dementia with Lewy bodies (DLB) is the recommended term for a common cause of dementia characterized by the histological presence of distinctive inclusions within neurons, Lewy bodies (McKeith et al, 1996). Following increasing pathological recognition, core clinical diagnostic features have been identified to allow diagnosis in life. Insights into the biology of this type of neurodegeneration suggest that the regional patterns of involvement might allow therapeutic intervention. Although Lewy bodies had long been recognized in the substantia nigra and other subcortical nuclei in patients with Parkinson's disease (PD), it was only in the 1970s that a significant number of reports began to be published from Japan describing patients with dementia and parkinsonism associated with the presence of Lewy bodies in cortical neurons (reviewed by Kosaka, 1990). Since these reports, different workers have used a variety of terms to describe this disease process, including diffuse Lewy body disease (Yoshimura, 1983), Lewy body dementia (Gibb et al, 1987), senile dementia of Lewy body type (Perry et al, 1990a) and the Lewy body variant of Alzheimer's disease (Hansen et al, 1990).

路易体痴呆。
路易小体痴呆(DLB)是一种常见的痴呆病因,其特征是神经元、路易小体内存在独特的组织学内含物(McKeith et al, 1996)。随着病理认识的增加,核心临床诊断特征已经确定,以便在生活中进行诊断。对这类神经退行性变生物学的深入研究表明,涉及的区域模式可能允许治疗干预。虽然路易小体在帕金森病(PD)患者的黑质和其他皮层下核中早就被发现,但直到20世纪70年代,日本才开始发表大量报告,描述痴呆和帕金森患者与皮层神经元中存在路易小体相关(Kosaka, 1990)。自这些报道以来,不同的工作者使用了各种术语来描述这一疾病过程,包括弥散性路易体病(Yoshimura, 1983)、路易体痴呆(Gibb et al, 1987)、路易体型老年痴呆(Perry et al, 1990a)和阿尔茨海默病的路易体变体(Hansen et al, 1990)。
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