| Literature DB >> 27344994 |
Naoko Mori1, Tamaki Ichikawa, Jun Hashimoto, Tomohiro Yamashita, Misuzu Yamada, Kenichi Hirabayashi, Yutaka Imai.
Abstract
Cholangiolocellular carcinoma (CoCC) is a rare primary liver cancer. It is considered to originate from hepatic progenitor or stem cells. We report a rare case of a 74-year-old male with CoCC of the liver and duodenal gastrointestinal stromal tumor (GIST). Both tumors manifested tracer uptakes on F-18 fluorodeoxyglucose positron emission tomography/computed tomography (F-18 FDG PET/CT); however, the uptake in hepatic tumor was extremely higher than that in the duodenal tumor. This finding was helpful to exclude the metastasis of GIST.Entities:
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Year: 2016 PMID: 27344994
Source DB: PubMed Journal: Tokai J Exp Clin Med ISSN: 0385-0005