A case of combined hepatocellular-cholangiocarcinoma with underlying schistosomiasis

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Abstract

Combined hepatocellular-cholangiocarcinoma is a rare form of primary liver cancer showing features of both hepatocellular and biliary epithelial differentiation. We report here on a case with collision tumor, which apparently was the coincidental occurrence of both hepatocellular carcinoma and cholangiocarcinoma underlying schistosomiasis. A 39-year-old-Philippine female was transferred to our hospital for evaluation of a liver mass that was found on ultrasonography at a local hospital. HBsAg and Anti-HCV were negative and serum alpha-fetoprotein (AFP) level was normal. The tumor mass was histologically diagnosed as adenocarcinoma by sono-guided biopsy before the operation. Partial lobectomy was performed and we histologically identified the concurrent occurrence of hepatocellular carcinoma and cholangiocarcinoma, (a "collision type carcinoma").

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Hong, C. K., Yang, J. M., Kang, B. K., Kim, J. D., Kim, Y. C., Chang, U. I., & Yoo, J. Y. (2007). A case of combined hepatocellular-cholangiocarcinoma with underlying schistosomiasis. Korean Journal of Internal Medicine, 22(4), 283–286. https://doi.org/10.3904/kjim.2007.22.4.283

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