cholangiohepatoma

cholangiohepatoma

 [ko-lan″je-o-hep″ah-to´mah]
primary carcinoma of the liver of mixed liver cell and bile duct cell origin.

cholangiohepatoma

A primary hepatic carcinoma of mixed liver cell and bile duct cell origin; the terms combined liver cell or bile duct carcinoma are sometimes preferred.

cho·lan·gi·o·hep·a·to·ma

(kŏ-lanjē-ō-hepă-tōmă)
Carcinoma of the bile duct and liver.
References in periodicals archive ?
ICD-Oncology code C22.0 was used to identify patients with PHN that included the following diagnostic groups: hepatocellular cancer, hepatic cell carcinoma, mixed hepatocellular carcinoma, fibrolamellar carcinoma, hepatocholangiolitic carcinoma, mixed bile duct with hepatocellular carcinoma, cholangiocarcinoma with hepatocellular carcinoma, cholangiohepatoma, hepatocarcinoma, hepatocholangiocarcinoma, and malignant embryonal hepatoma.