Ince P G, Perry E K, Morris C M
University of Newcastle upon Tyne, and Department of Neuropathology, Newcastle General Hospital, UK.
Brain Pathol. 1998 Apr;8(2):299-324. doi: 10.1111/j.1750-3639.1998.tb00156.x.
Lewy body formation is central to the pathological phenotype of a spectrum of disorders. The most familiar of these is the extrapyramidal syndrome of idiopathic Lewy-body Parkinson's disease (PD). Studies of dementia in the elderly suggest that another manifestation of Lewy body pathology is equally or more common than Parkinson's disease. This syndrome of Dementia with Lewy bodies (DLB) has been given a number of diagnostic labels and is characterised by dementia, relatively mild parkinsonism, visual hallucinations, and fluctuations in conscious level. Although many of these features can arise in Parkinson's disease, the patients with DLB tend to have early neuropsychiatric features which predominate the clinical picture, and the diagnosis of the syndrome in practice is more concerned with the differential diagnosis of Alzheimer's disease (AD). Distinction from AD has clinical importance because of potentially differing therapeutic implications. Diagnostic guidelines for the clinical diagnosis and pathological evaluation of DLB are reviewed. Research into the disorder has centered around characterising the clinical, neuropsychological, pathological, neurochemical and genetic relationships with Alzheimer's disease on the one hand, and Parkinson's disease on the other. Many cases of DLB have prominent pathological features of AD and there are some shared genetic risk factors. Differences from the pathology of PD are predominantly quantitative rather than qualitative and evidence is discussed which suggests that DLB represents a clinicopathological syndrome within the spectrum of Lewy body disorders. The possibility that the syndrome represents a chance association of PD and AD is not supported by published studies.
路易小体的形成是一系列疾病病理表型的核心。其中最常见的是特发性路易体帕金森病(PD)的锥体外系综合征。对老年人痴呆症的研究表明,路易体病理的另一种表现形式与帕金森病同样常见或更为常见。这种路易体痴呆综合征(DLB)有多种诊断标签,其特征为痴呆、相对较轻的帕金森症状、视幻觉以及意识水平波动。尽管这些特征中的许多也可能出现在帕金森病中,但DLB患者往往有早期神经精神症状,这些症状在临床表现中占主导地位,并且在实际中该综合征的诊断更多地涉及与阿尔茨海默病(AD)的鉴别诊断。由于潜在的治疗意义不同,与AD的区分具有临床重要性。本文综述了DLB临床诊断和病理评估的诊断指南。对该疾病的研究一方面围绕其与AD以及另一方面与帕金森病在临床、神经心理学、病理、神经化学和遗传学方面的关系进行特征描述。许多DLB病例具有AD的显著病理特征,并且存在一些共同的遗传风险因素。与PD病理的差异主要是数量上的而非质量上的,文中讨论了相关证据,表明DLB代表路易体疾病谱中的一种临床病理综合征。已发表的研究不支持该综合征是PD和AD偶然关联的可能性。