Metastatic Kaposi sarcoma with osseous involvement in a patient with AIDS

Mariola Vazquez-Martinez, Erika Correa, B. Agarwal, Jingxu Zhou, S. Soundararajan, P. Lothe, M. Jain
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引用次数: 1

Abstract

Kaposi sarcoma is an AIDS-defining illness associated with human herpes virus-8 (HHV-8) co-infection. It was described in 1872 by the Hungarian dermatologist Mortiz Kaposi, and was an isolated and sporadic occurrence before the emergence of HIV infection and AIDS.1 It was first affiliated as an AIDS-associated neoplasm in 1981.1 Kaposi sarcoma is a systemic disease that can present with cutaneous lesions with or without internal involvement. There are four subtypes: Classic, African endemic, AIDS-related (CD4 count, <200), and Kaposi sarcoma in iatrogenically immunosuppressed patients. The disease has the propensity to manifest in the skin and gastro-intestinal and respiratory tracts, and osseous involvement is rarely encountered. We present here the case of an AIDS-positive man with generalized bone pain as a result of metastasis from Kaposi sarcoma. Our discussion includes the epidemiological, clinical, pathological, and radiological facets of AIDS-related Kaposi sarcoma, and the anomaly of osseous involvement.
艾滋病患者的转移性卡波西肉瘤伴骨骼受累
卡波西肉瘤是一种与人类疱疹病毒-8(HHV-8)共同感染相关的艾滋病定义性疾病。1872年,匈牙利皮肤科医生Mortiz Kaposi对其进行了描述,在HIV感染和艾滋病出现之前,它是一种孤立和散发的疾病。1 1981年,它首次被列为艾滋病相关肿瘤。1.1 Kaposi肉瘤是一种全身性疾病,可以有或无内部受累的皮肤病变出现。医源性免疫抑制患者有四种亚型:经典型、非洲地方性、艾滋病相关型(CD4计数<200)和卡波西肉瘤。这种疾病倾向于在皮肤、胃肠道和呼吸道表现出来,很少发生骨受累。我们在这里提出一个艾滋病阳性男子的病例,由于转移卡波西肉瘤引起全身骨痛。我们的讨论包括艾滋病相关卡波西肉瘤的流行病学、临床、病理学和放射学方面,以及骨受累的异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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