Institut de Neuropatologia, Servei Anatomia Patològica, IDIBELL-Hospital Universitari de Bellvitge, 08907 Hospitalet de LLobregat, Spain.
J Neurol Sci. 2010 Dec 15;299(1-2):139-49. doi: 10.1016/j.jns.2010.08.039. Epub 2010 Sep 16.
The term cognitive impairment of vascular origin is used to designate global cognitive deficits as well as focal neurological deficits such as aphasia, apraxia and agnosia of vascular/circulatory origin. It has been useful for identifying early clinical and neuroradiological alterations that might permit therapeutic strategies geared to curbing the progression of cerebrovascular disease. Multi-infarct encephalopathy, infarcts in strategic areas, lacunae and lacunar status, Binswanger's encephalopathy, hippocampal sclerosis, cortical granular atrophy and watershed infarcts are common lesions. Hypertension and vascular diseases such as arteriosclerosis, small blood vessel disease, inflammatory diseases of the blood vessels, Sneddon syndrome, cerebral amyloid angiopathies, cerebral autosomic dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), and Maeda's syndrome are causative of cognitive impairment of vascular origin. Other less common causes are hereditary endotheliopathy with retinopathy, neuropathy and strokes (HERNS), cerebro-retinian vasculopathy (CRV), hereditary vascular retinopathy (HVR) (all three linked to 3p21.1-p21.3), hereditary infantile hemiparesis with arteriolar retinopathy and leukoencephalopathy (HIHRATL) (not linked to 3p21), fibromuscular dysplasia, and moya-moya disease. Lack of uniformity of clinical manifestations, the variety of vascular diseases and circulatory factors, the diverse, but often convergent, neuropathological substrates, and the common association with unrelated neurodegenerative diseases in the elderly, make it hard to assume a single clinical approach in the diagnosis and treatment of cognitive impairment of vascular origin. Rather, environmental and genetic risk factors, underlying vascular diseases, associated systemic, metabolic and neurodegenerative diseases and identification of extent and distribution of lesions with morphological and functional neuroimaging methods should be applied in every individual patient.
血管性认知障碍这一术语用于指代由血管/循环原因引起的全面认知障碍,以及局灶性神经功能缺损,如血管性失语症、失用症和失认症。它有助于识别早期的临床和神经影像学改变,这些改变可能使我们能够采取治疗策略来阻止脑血管疾病的进展。多发性脑梗死性痴呆、战略区域梗死、腔隙和腔隙状态、Binswanger 脑病、海马硬化、皮质颗粒萎缩和分水岭梗死是常见的病变。高血压和血管疾病,如动脉硬化、小血管疾病、血管炎性疾病、Sneddon 综合征、脑淀粉样血管病、伴有皮质下梗死和白质脑病的脑常染色体显性动脉病(CADASIL)和 Maeda 综合征,是血管性认知障碍的病因。其他不太常见的病因是伴有视网膜病变、神经病和中风的遗传性内皮病(HERNS)、脑视网膜血管病(CRV)、遗传性血管视网膜病(HVR)(均与 3p21.1-p21.3 相关)、伴有小动脉视网膜病变和白质脑病的遗传性婴儿偏瘫(HIHRATL)(不与 3p21 相关)、纤维肌性发育不良和 moya-moya 病。临床表现缺乏一致性,血管疾病和循环因素多种多样,神经病理学基础各不相同,但往往趋同,以及老年人常见的与无关的神经退行性疾病的共同关联,使得很难在血管性认知障碍的诊断和治疗中采用单一的临床方法。相反,应该在每个患者中应用环境和遗传风险因素、潜在的血管疾病、相关的系统性、代谢和神经退行性疾病以及使用形态和功能神经影像学方法来识别病变的程度和分布。