Erkinjuntti T
Acta Neurol Scand. 1987 Jun;75(6):391-9. doi: 10.1111/j.1600-0404.1987.tb05467.x.
A series of 79 patients with multi-infarct dementia (MID) were divided into 2 groups designated cortical MID and subcortical MID, according to whether the computed tomography (CT) scan showed the presence or absence of cortical infarcts, and an absent to mild or moderate to severe degree of white matter low attenuation (WMLA). Cortical MID was characterized by repeated atherothrombotic and cardiogenic strokes, moto-sensory hemiparesis, a severer degree of aphasia, and abrupt onset of cognitive failure. Subcortical MID typically showed the following features: lacunar strokes, bulbar signs including dysarthria, pure motor hemiparesis, depression and emotional lability. WMLA was found in all patients with subcortical MID but also in over 60% of those with cortical MID. In the 2 groups CT scans showed equal frequencies of deep infarcts. When divided according to severity of WMLA, 92% of patients in the cortical MID group and 44% of those in the subcortical MID group were found to have at least one cortical infarct on the CT scan. Although cortical and subcortical MID differed in several clinical features, they did not show major differences in the risk factors for stroke, and clearly overlapped each other as regards ischaemic scores and the findings in neurological examinations and CT. Thus, it is still an open question whether cortical MID and subcortical MID, including the lacunar state and Binswanger's disease, are 2 distinct entities or merely represent the expression of biological variation while having the same etiopathogenesis.
根据计算机断层扫描(CT)显示有无皮质梗死以及有无轻度至中度或重度白质低衰减(WMLA),将79例多梗死性痴呆(MID)患者分为两组,即皮质型MID和皮质下型MID。皮质型MID的特征为反复发生动脉粥样硬化血栓形成性和心源性中风、运动感觉性偏瘫、更严重的失语症以及认知功能突然衰退。皮质下型MID通常表现出以下特征:腔隙性中风、包括构音障碍在内的延髓体征、纯运动性偏瘫、抑郁和情绪不稳定。所有皮质下型MID患者均发现有WMLA,但皮质型MID患者中超过60%也有WMLA。两组CT扫描显示深部梗死的频率相同。根据WMLA的严重程度进行划分时,皮质型MID组92%的患者和皮质下型MID组44%的患者在CT扫描中发现至少有一处皮质梗死。尽管皮质型和皮质下型MID在若干临床特征上有所不同,但它们在中风危险因素方面并未显示出重大差异,在缺血评分以及神经检查和CT检查结果方面明显相互重叠。因此,皮质型MID和皮质下型MID,包括腔隙状态和宾斯旺格病,究竟是两个不同的实体,还是仅仅代表具有相同病因发病机制的生物学变异的表现,仍然是一个悬而未决的问题。