Ye M-F, Zheng S, Xu J-H, Chen L-R
Cancer Institute, The Second Affiliated Hospital, School of Medicine, Zhejiang University, China.
Histol Histopathol. 2007 Dec;22(12):1337-42. doi: 10.14670/HH-22.1337.
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.
肝脏原发性恶性纤维组织细胞瘤(MFH)极为罕见,文献中仅报道过几例。我们报告一例53岁男性的肝脏MFH病例,该患者出现上腹部疼痛及体重减轻1个月。超声和计算机断层扫描(CT)显示肝脏左叶有一个伴有细小肿瘤血管的大肿块。组织病理学检查结果表明这是一个间叶性肿瘤,由呈束状排列的梭形细胞与组织细胞样细胞和巨细胞混合组成。免疫组织化学检查显示,大多数肿瘤细胞表达波形蛋白、α-1抗糜蛋白酶、α-1抗胰蛋白酶和CD68。形态学和免疫组织化学检查结果支持该肿瘤应归类为原发性恶性纤维组织细胞瘤。本文对相关文献进行了简要综述。