肝破骨细胞样巨细胞瘤(OGCT

隆祐 松本, 晃 吉田, 淳 中島, 智文 新, 剛 竹田, 秀之 柳澤, 英明 菊池, 慶介 菊地
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引用次数: 1

摘要

男性,57岁,黄疸。腹部ct示左侧肝叶10cm不均匀实性肿块,肿块内低衰减区,多发肝转移及肺转移。乙肝和丙肝血清学均为阴性。血清甲胎蛋白、CEA、CA19-9正常。几周后,患者死于进行性肝功能衰竭,并进行了尸检。组织学上,肿瘤由肉瘤样单核细胞和破骨细胞样巨细胞组成。肿瘤周围的肝组织未见肝硬化。破骨细胞样巨细胞对CD68呈均匀且强烈的免疫反应。单核细胞表达vimentin, CAM5.2表达阴性。单核细胞的mb -1指数为20%。总之,组织病理学诊断为肝脏破骨细胞样巨细胞瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
osteoclast-like giant cell tumor(OGCT)of the liverの1剖検例
: A 57-year-old man presented with jaundice. Abdominal computed tomography showed a 10-cm left hepatic lobe heterogeneous solid mass with low attenuated areas in the mass, multiple liver metastases and lung metastasis. Serology for hepatitis B and C were negative. Serum alpha-fetoprotein, CEA and CA19-9 were normal. The patient died a few weeks later of progressive liver failure and an autopsy was performed. Histologically, the tumor consisted of sarcomatoid mononuclear cells and osteoclast-like giant cells. The liver tissue surrounding the tumor showed no cirrhotic pattern. The osteoclast-like giant cells were uniformly and strongly immunoreactive with CD68. The mononuclear cells demonstrated expression of vimentin but were negative for CAM5.2. The MIB-1 index was 20% for the mononuclear cells. In conclusion, the histopathological diagnosis revealed an osteoclast-like giant cell tumor of the liver.
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