Navia B A, Cho E S, Petito C K, Price R W
Ann Neurol. 1986 Jun;19(6):525-35. doi: 10.1002/ana.410190603.
In order to define the histopathological substrate of the dementia that frequently complicates the acquired immune deficiency syndrome (AIDS), we analyzed the neuropathological findings in 70 autopsied adult AIDS patients, 46 of whom had suffered clinically overt dementia. Less than 10% of the brains were histologically normal. Abnormalities were found predominantly in the white matter and in subcortical structures, with relative sparing of the cortex. Their frequency and severity generally correlated well with the degree and duration of clinical dementia. Most commonly noted was diffuse pallor in the white matter, which in the pathologically milder cases was accompanied by scanty perivascular infiltrates of lymphocytes and brown-pigmented macrophages, and in the most advanced cases by clusters of foamy macrophages and multinucleated cells associated with multifocal rarefaction of the white matter. However, in nearly one third of the demented cases the histopathological findings were remarkably bland in relation to the severity of clinical dysfunction. In addition, similar mild changes were noted in over one half of the nondemented patients, consistent with subclinical involvement. Vacuolar myelopathy was found in 23 patients and was generally more common and severe in patients with advanced brain pathology. Evidence of cytomegalovirus (CMV) infection was noted in nearly one quarter of the brains and was associated with a relative abundance of microglial nodules, but correlated neither with the major subcortical neuropathology nor with the clinical dementia, indicating that CMV infection likely represented a second, superimposed process. This study establishes the AIDS dementia complex as a distinct clinical and pathological entity and, together with accumulating virological evidence, suggests that it is caused by direct LAV/HTLV-III brain infection.
为了明确常并发于获得性免疫缺陷综合征(AIDS)的痴呆的组织病理学基础,我们分析了70例成年AIDS患者尸检的神经病理学发现,其中46例有明显的临床痴呆症状。不到10%的脑在组织学上是正常的。异常主要见于白质和皮质下结构,皮质相对 spared。其频率和严重程度一般与临床痴呆的程度和持续时间密切相关。最常见的是白质弥漫性苍白,在病理较轻的病例中伴有少量淋巴细胞和棕色色素巨噬细胞的血管周围浸润,在最严重的病例中伴有泡沫状巨噬细胞和多核细胞簇,伴有白质多灶性稀疏。然而,在近三分之一的痴呆病例中,组织病理学发现与临床功能障碍的严重程度相比明显平淡。此外,超过一半的非痴呆患者也有类似的轻微变化,与亚临床受累一致。23例患者发现有空泡性脊髓病,在脑病理晚期的患者中通常更常见且更严重。近四分之一的脑有巨细胞病毒(CMV)感染的证据,与相对丰富的小胶质结节有关,但与主要的皮质下神经病理学及临床痴呆均无相关性,表明CMV感染可能代表了第二个叠加过程。本研究将AIDS痴呆综合征确立为一种独特的临床和病理实体,并与越来越多的病毒学证据一起表明,它是由LAV/HTLV-III直接感染脑所致。