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A Rare Occurrence of Primary Hepatic Leiomyosarcoma Associated with Epstein Barr Virus Infection in an AIDs Patient

机译:艾滋病患者中原发性肝平滑肌肉瘤与爱泼斯坦巴尔病毒感染相关的罕见发生

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摘要

Primary hepatic leiomyosarcoma is exceedingly rare accounting for less than 1% of the hepatic tumors. Close to 45 cases have been reported in the English literature. Presentation is usually nonspecific and diagnosis is often delayed until tumors reach a large size. This leads to a dismal prognosis. The tumors are not yet fully understood, hence the standard of care is not well defined. Curative resection remains the mainstay of management. Close association of Epstein Barr virus (EBV) induced soft tissue sarcomas is proven, especially in the presence of immunosuppression encountered in HIV/AIDS patients and in posttransplant patients. We herein present a case report of a 54-year-old man diagnosed to have HIV/AIDS and EBV infection admitted to our hospital with complaints of intractable hiccups for more than a week. Extensive workup revealed primary leiomyosarcoma of the liver.
机译:原发性肝平滑肌肉肉瘤非常罕见,占不到肝肿瘤的1%。英文文献中已报道了近45例。表现通常是非特异性的,并且诊断通常会延迟到肿瘤达到较大尺寸为止。这导致预后不良。尚未完全了解肿瘤,因此治疗标准尚不明确。根治性切除仍然是管理的支柱。事实证明,爱泼斯坦巴尔病毒(EBV)引起的软组织肉瘤紧密相关,尤其是在存在HIV / AIDS患者和移植后患者出现免疫抑制的情况下。我们在此提供一例54岁男性的病例报告,该男性被诊断患有HIV / AIDS和EBV感染,因顽固性打ic持续了一个多星期而入院。大量检查发现原发性肝平滑肌肉瘤。

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