Kleihues P, Lang W, Burger P C, Budka H, Vogt M, Maurer R, Lüthy R, Siegenthaler W
Acta Neuropathol. 1985;68(4):333-9. doi: 10.1007/BF00690837.
Two adult patients with acquired immune deficiency syndrome (AIDS) presented with psycho-organic symptoms produced by an extensive cerebral and cerebellar leukoencephalopathy. Diffuse loss of myelin and axons with reactive astrocytosis and distinctive multinucleated giant cells were prominent in the deep white matter, but less so in the subcortical white matter and in compact myelinated pathways. Bilateral involvement of the centrum semiovale produced distal Wallerian degeneration of the descending pyramidal tracts, which in one patient correlated with progressive paraparesis and bladder dysfunction. Although there were morphological indications of cytomegalovirus infection and immunohistochemical evidence of papovavirus antigens, the neuropathology did not resemble that usually associated with infection by these opportunistic agents. The possibility is entertained that the progressive diffuse leukoencephalopathy (PDL) in these patients was directly related to infection with human T-cell lymphotropic virus (HTLV-III/LAV), the etiologic agent of AIDS.
两名成年获得性免疫缺陷综合征(AIDS)患者出现由广泛的大脑和小脑白质脑病引起的精神器质性症状。在深部白质中,髓鞘和轴突弥漫性丧失,伴有反应性星形细胞增生和独特的多核巨细胞,而在皮质下白质和紧密髓鞘化通路中则较少见。半卵圆中心的双侧受累导致下行锥体束的远心性华勒氏变性,其中一名患者的这种变性与进行性截瘫和膀胱功能障碍相关。尽管有巨细胞病毒感染的形态学指征和乳头多瘤空泡病毒抗原的免疫组化证据,但神经病理学表现并不类似于通常与这些机会性病原体感染相关的表现。人们推测这些患者的进行性弥漫性白质脑病(PDL)与人类嗜T淋巴细胞病毒(HTLV-III/LAV,即AIDS的病原体)感染直接相关。