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Clin Mol Hepatol ; 20(4): 406-10, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25548749

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