Robert M E, Geraghty J J, Miles S A, Cornford M E, Vinters H V
Department of Pathology, UCLA Medical Center 90024-1732.
Acta Neuropathol. 1989;79(3):255-61. doi: 10.1007/BF00294659.
A patient with acquired immune deficiency syndrome (AIDS) developed a progressive neuromuscular disorder which included a sensory component, severe weakness and muscle wasting, and fasciculations. At autopsy, there was evidence of severe peripheral neuropathy, as well as widespread cytomegalovirus (CMV) infection within the central and peripheral nervous system. Although the anterior horn cell complement within the spinal cord appeared normal, there was also evidence of human immunodeficiency virus (HIV)-like immunoreactivity of rare anterior horn cells, as judged by immunohistochemical staining. This patient illustrates the complexity of pathogenetic mechanisms operative in AIDS patients with neuromuscular disease, and suggests that at least some examples of neuromuscular disease in patients with this syndrome may be related to widespread CMV infection of the peripheral nerve (including microvascular endothelial cells) and, more rarely, direct HIV infection of some anterior horn cells.
一名获得性免疫缺陷综合征(艾滋病)患者出现了一种进行性神经肌肉疾病,其症状包括感觉成分、严重虚弱、肌肉萎缩和肌束震颤。尸检时,有证据表明存在严重的周围神经病变,以及中枢和周围神经系统内广泛的巨细胞病毒(CMV)感染。尽管脊髓前角细胞成分看起来正常,但通过免疫组织化学染色判断,也有罕见的前角细胞存在人类免疫缺陷病毒(HIV)样免疫反应性的证据。该患者说明了艾滋病合并神经肌肉疾病患者发病机制的复杂性,并提示该综合征患者的神经肌肉疾病至少有一些病例可能与周围神经(包括微血管内皮细胞)的广泛CMV感染有关,更罕见的是,与一些前角细胞的直接HIV感染有关。