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Clinical and Molecular Hepatology ; : 406-410, 2014.
Article in English | WPRIM | ID: wpr-85676

ABSTRACT

Bi-phenotypic neoplasm refers to tumors derived from a common cancer stem cell with unique capability to differentiate histologically into two distinct tumor types. Bi-phenotypic hepatocellular carcinoma-cholangiocarcinoma (HCC-CC), although a rare tumor, is important for clinicians to recognize, since treatment options targeting both elements of the tumor are crucial. Imaging findings of bi-phenotypic HCC-CC are not specific and include features of both HCC and CC. A combination of imaging and immuno-histochemical analysis is usually needed to make the diagnosis.


Subject(s)
Humans , CA-19-9 Antigen/metabolism , Carcinoma, Hepatocellular/mortality , Cholangiocarcinoma/mortality , Liver Neoplasms/mortality , Magnetic Resonance Imaging , Phenotype , Risk Factors , Survival Analysis , Tomography, X-Ray Computed , alpha-Fetoproteins/analysis
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