Abstract
We experienced a rare case of intraductal (common hepatic duct) hepatocellular carcinoma. Review of theliterature disclosed 30 cases or less in which common duct involvement was a predominent clinical feature. Well demarcated, ovoid filling defect mass in CHD without parencyhymal tumor mass was noted in ultrasound, PTC&CTstudy. The liver was cirrhotic, but alpa-fetoprotein level was normal. Defferential diagnosis especially withKlatskin tumor is important and thought to be possible.