The neuropathology of vascular dementia

Gustavo C. Román, Oscar Benavente
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引用次数: 12

Abstract

Ischemic infarction is the main lesion underlying vascular dementia (VaD) but cases also occur after brain hemorrhage, as well as with hypoperfusive brain ischemia. Ischemic strokes include large-vessel cortico-subcortical strokes and lacunes resulting from small-vessel disease. Arteriolosclerosis and fibrinoid necrosis are the most common forms of small-vessel disease in the elderly. Although it was originally proposed that vascular dementia could result from repeated strokes with loss of >100 mL of brain tissue loss (multi-infarct dementia), it is currently held that the location of the stroke is probably more relevant to cognitive loss and dementia. In fact, a single, strategically located stroke may interrupt cortico-subcortical circuits important for memory and cognition. Hypoperfusive lesions include border-zone cortico-subcortical infarcts, temporal lobe sclerosis, and periventricular incomplete ischemic leukoencephalopathy. The latter two lesions are commonly seen in the elderly as a result of narrowing and tortuosity of medullary arterioles irrigating these distal territories, plus cardiac pump failure. Binswanger disease is characterized by extensive periventricular ischemic leukoencephalopathy that spares the arcuate U-fibers, and presence of lacunar strokes. CADASIL is a genetic form of vascular dementia characterized by a cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. CADASIL is due to a mutation of the Notch3 gene in chromosome 19. Intracerebral hemorrhages in strategic locations may produce vascular dementia. Lesions in the basal forebrain that damage cholinergic nuclei, such as those resulting from a ruptured aneurysm of the anterior communicating artery, may produce vascular dementia. Some patients with subarachnoid hemorrhage develop normal-pressure hydrocephalus. Cerebral amyloid angiopathy (congophilic angiopathy) may cause lobar hemorrhages and dementia. Vascular lesions, in particular, microinfarcts, are frequently found in patients with a clinical diagnosis of Alzheimer disease. These mixed forms of dementia are likely to become the most common form of dementia in the elderly.

血管性痴呆的神经病理学
缺血性梗死是血管性痴呆(VaD)的主要病变,但也发生在脑出血和低灌注脑缺血后。缺血性中风包括大血管皮质-皮质下中风和由小血管疾病引起的脑陷窝。小动脉硬化和纤维蛋白样坏死是老年人最常见的小血管疾病。虽然最初提出血管性痴呆可能是由反复中风导致的>100 mL脑组织损失(多梗死性痴呆),但目前认为中风的部位可能与认知丧失和痴呆更相关。事实上,一次有策略的中风可能会中断对记忆和认知很重要的皮质-皮质下回路。低灌注损伤包括皮质-皮质下边界区梗死、颞叶硬化和脑室周围不完全缺血性脑白质病。后两种病变常见于老年人,是由于髓小动脉狭窄和扭曲,再加上心脏泵功能衰竭。Binswanger病的特点是广泛的脑室周围缺血性脑白质病,不包括弓形u纤维,并存在腔隙性中风。CADASIL是一种血管性痴呆的遗传形式,其特征是大脑常染色体显性动脉病变伴皮层下梗死和脑白质病。CADASIL是由19号染色体上的Notch3基因突变引起的。重要部位的脑出血可引起血管性痴呆。基底前脑损伤胆碱能核,如由前交通动脉动脉瘤破裂引起的损伤,可产生血管性痴呆。一些蛛网膜下腔出血的患者发展为常压脑积水。脑淀粉样血管病(嗜血性血管病)可引起大叶出血和痴呆。血管病变,特别是微梗死,经常在临床诊断为阿尔茨海默病的患者中发现。这些混合形式的痴呆症很可能成为老年人中最常见的痴呆症。
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