A case of fibrous histiocytoma of the liver.

T Maekawa, K Yabuki, K Sato, Y Tamasaki, H Maekawa, K Ogawa, A Hirano, M Eguchi, M Matsumoto
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Abstract

Malignant fibrous histiocytoma (MFH) is a rare disease. We describe a 68-year-old man admitted to the hospital because of malaise. On admission, hematologic and serum chemical examinations showed no abnormalities. A tumor measuring 6.0 x 6.0 x 5.5 cm was found in segment S6 of the right lobe of the liver. A computed tomographic scan of the abdomen revealed a mass surrounded by a capsule-like region with a nonuniform shadow at its margin. The mass contained a nonuniform low density area. A magnetic resonance imaging scan showed low intensity on T1-weighted images and high intensity on T2-weighted images. An angiogram of the abdomen revealed a tumor with a darkly stained margin during the venous phase. Partial resection of the liver, including S6 and part of S7, was performed. On histopathological examination, this case was characterized by a storiform pattern. The inside of the tumor showed a storiform-pleomorphic pattern with inflammatory cell infiltration and partial mucinous degeneration. On immunohistochemical studies, the tumor cells stained positively for CD6. The diagnosis was MFH.

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肝纤维组织细胞瘤1例。
恶性纤维组织细胞瘤是一种罕见的疾病。我们描述了一位68岁的男子,因为身体不适而入院。入院时,血液学及血清化学检查未见异常。肝右叶S6节段肿瘤大小为6.0 x 6.0 x 5.5 cm。腹部计算机断层扫描显示肿块周围有一个囊状区域,边缘有不均匀的阴影。质量包含一个不均匀的低密度区域。磁共振成像扫描显示低强度t1加权像和高强度t2加权像。腹部血管造影显示静脉期有一肿瘤,边缘呈黑色染色。切除部分肝脏,包括S6和部分S7。在组织病理学检查中,该病例的特点是故事状模式。肿瘤内部呈层状多形性,伴炎性细胞浸润及部分黏液变性。免疫组化结果显示肿瘤细胞CD6阳性。诊断为MFH。
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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[Pulmonary hypertension]. [Oral chemotherapeutic agents: the roles in cancer chemotherapy]. Evaluation by microdensitometry and dual energy X-ray absorptiometry of changes in bone metabolism after gastrectomy. Changes in volumetric bone mineral density after gastrectomy as assessed by dual energy X-ray absorptiometry. A case of fibrous histiocytoma of the liver.
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