Gherardi R K
Department of Pathology (Neuropathology), Hôpital Henri Mondor, Créteil, France.
Neuropathol Appl Neurobiol. 1994 Jun;20(3):232-7. doi: 10.1111/j.1365-2990.1994.tb00964.x.
Skeletal muscle involvement may occur at all stages of human immunodeficiency virus (HIV)-infection, and represents the first manifestation of the disease in some patients. There have been many controversies about the classification of myopathies related to HIV infection. We usually classify muscle involvement in HIV-infected patients in one of the following categories: (1) HIV-associated myopathy, a myopathy that meets the criteria for polymyositis in a majority of patients, and those for acquired nemaline myopathy in some; (2) zidovudine myopathy, a reversible mitochondrial myopathy; (3) the HIV-wasting syndrome and other AIDS-associated cachexias; (4) opportunistic infections and tumoral infiltrations of skeletal muscle; (5) vasculitic processes and iron pigment deposits. Immunohistology for major histocompatibility complex class I antigen and the histochemical reaction for cytochrome C oxidase are helpful in correctly classifying a myopathy as HIV polymyositis or zidovudine myopathy respectively. Studies of circulating levels and tissue expression of cytokines in HIV-infected patients have yielded new insights into the pathogenesis of the various AIDS-associated muscle disorders.
骨骼肌受累可发生在人类免疫缺陷病毒(HIV)感染的各个阶段,并且在一些患者中是该疾病的首发表现。关于与HIV感染相关的肌病分类存在许多争议。我们通常将HIV感染患者的肌肉受累分为以下类别之一:(1)HIV相关肌病,大多数患者符合多发性肌炎标准,部分患者符合获得性杆状肌病标准;(2)齐多夫定肌病,一种可逆的线粒体肌病;(3)HIV消瘦综合征及其他与艾滋病相关的恶病质;(4)骨骼肌的机会性感染和肿瘤浸润;(5)血管炎过程和铁色素沉积。主要组织相容性复合体I类抗原的免疫组织化学和细胞色素C氧化酶的组织化学反应分别有助于正确地将肌病分类为HIV多发性肌炎或齐多夫定肌病。对HIV感染患者细胞因子循环水平和组织表达的研究为各种与艾滋病相关的肌肉疾病的发病机制提供了新的见解。