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成人肝横纹肌肉瘤:一种罕见的原发性肝脏恶性肿瘤。病例报告及文献综述。

Hepatic rhabdomyosarcoma in an adult: a rare primary malignant liver tumor. Case report and literature review.

作者信息

Schoofs G, Braeye L, Vanheste R, Verswijvel G, Debiec-Rychter M, Sciot R

机构信息

Department of Gastroenterology, University Hospital Leuven, Belgium.

出版信息

Acta Gastroenterol Belg. 2011 Dec;74(4):576-81.

PMID:22319971
Abstract

Rhabdomyosarcomas are malignant tumors that display features of striated muscle differentiation. They are the most common soft-tissue sarcomas among children and young adults. In mature adults however there are very rare. The liver as a primary site in adults has only been described in 12 cases. We report a case of a primary alveolar rhabdomyosarcoma of the liver in a 59 year old female, confirmed by histological examination using immunohistochemical analysis (positive actin, desmin, vimentin and myogenin staining) and fluorescent in situ hybridization (FISH) analysis (positivity for PAX3/FOXO1A fusion). The patient underwent primary surgical resection, but presented a few weeks after surgery already with recurrent disease in the abdomen and bone metastasis. Despite initial good response to chemotherapy (doxorubicin/ifosfamide) and stable disease at 12 months after diagnosis, the patient died 31 months after the first presentation secondary to complicated abundant abdominal recurrent disease. We further present a review of the literature on published similar cases since 1979.

摘要

横纹肌肉瘤是一种具有横纹肌分化特征的恶性肿瘤。它们是儿童和青年中最常见的软组织肉瘤。然而,在成年人中非常罕见。肝脏作为成年人的原发部位仅在12例病例中被描述过。我们报告一例59岁女性肝脏原发性肺泡横纹肌肉瘤病例,通过免疫组织化学分析(肌动蛋白、结蛋白、波形蛋白和肌细胞生成素染色阳性)和荧光原位杂交(FISH)分析(PAX3/FOXO1A融合阳性)进行组织学检查得以确诊。该患者接受了初次手术切除,但术后几周就出现了腹部复发性疾病和骨转移。尽管最初对化疗(阿霉素/异环磷酰胺)反应良好且诊断后12个月病情稳定,但患者在首次就诊31个月后因复杂的大量腹部复发性疾病继发死亡。我们还进一步回顾了自1979年以来已发表的类似病例的文献。

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