Department of Pathology, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Semin Liver Dis. 2010 Feb;30(1):107-12. doi: 10.1055/s-0030-1247137. Epub 2010 Feb 19.
The authors present the case of a 48-year-old man with hepatitis B cirrhosis, who developed two primary malignant liver tumors that were morphologically distinct from each other. The first tumor was a hepatocellular carcinoma and the second tumor, detected 17 months later was a hepatic carcinosarcoma with cholangiocarcinomatous and sarcomatous components, without any hepatocellular carcinoma component. Clonality studies using microsatellite-based loss of heterozygosity (LOH) demonstrated different LOH patterns existed between the hepatocellular carcinoma and the hepatic carcinosarcoma, indicative of different clonal origins. The authors discuss the histogenesis, histopathologic diagnosis, and clinical behavior of hepatic carcinosarcoma.
作者报告了一例 48 岁男性乙型肝炎肝硬化患者,该患者发生了两个形态上彼此不同的原发性恶性肝肿瘤。第一个肿瘤为肝细胞癌,第二个肿瘤在 17 个月后被检测出为具有胆管癌和肉瘤成分的肝癌肉瘤,而没有任何肝细胞癌成分。使用基于微卫星的杂合性丢失(LOH)的克隆性研究表明,肝细胞癌和肝癌肉瘤之间存在不同的 LOH 模式,表明具有不同的克隆起源。作者讨论了肝癌肉瘤的组织发生、组织病理学诊断和临床行为。
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