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HOME > Clin Endosc > Volume 13(2); 1993 > Article
Clinical Endoscopy 1993;13(2):419-423.
DOI: https://doi.org/
Published online: November 30, 1992
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Cholangiocarcinoma is a rare tumor among all populations of the world and accounts for less than 2% of cancers found at autopsy and between 10% and 20% of all primary liver cancers. The tumor originates either from the intrahepatic small duct radicles(peripheral type) or the major hepatic ducts at or near the junction of the right and left hepatic ducts(hilar type). Included in the latter are the small intraduct carcinomas arising at the bifurcation of the hepatic ducts. (continue...)


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