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Primary hepatic malignant fibrous histiocytoma: a case report and review of the literature.

机译:原发性肝恶性纤维组织细胞瘤:一例报道并文献复习。

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Primary malignant fibrous histiocytoma (MFH) of the liver remains extremely rare with only several cases having been reported in literature. We report a case of hepatic MFH in a 53-year-old man who presented with upper abdominal pain, and weight loss for one month. Ultrasound and computed tomography (CT) scan showed a large mass with fine tumor vessels over the left lobe of the liver. Histopathological findings indicated a mesenchymal tumor consisting of spindle cells in storiform pattern intermingled with histiocyte-like cells and giant cells. Immunohistochemically, most tumor cells expressed vimentin, alpha-1 anti-chymotrypsin, alpha-1 antitrypsin and CD68. Morphological and immunohistochemical findings support that the tumor should be classified as a primary malignant fibrous histiocytoma. The literatures is briefly reviewed.
机译:肝脏原发性恶性纤维组织细胞瘤(MFH)仍然极为罕见,文献中仅报道了几例。我们报告了一位53岁的男性患者出现肝MFH的情况,该患者出现上腹部疼痛,体重减轻了一个月。超声和计算机断层扫描(CT)扫描显示肿块较大,在肝脏左叶上方有细小的肿瘤血管。组织病理学发现表明间充质瘤由梭形样梭形细胞与组织细胞样细胞和巨细胞混合而成。免疫组织化学分析,大多数肿瘤细胞表达波形蛋白,α-1抗胰凝乳蛋白酶,α-1抗胰蛋白酶和CD68。形态学和免疫组化结果支持将肿瘤归为原发性恶性纤维组织细胞瘤。文献简要回顾。

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