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Clinical and Molecular Hepatology ; : 406-410, 2014.
Artículo en Inglés | WPRIM | ID: wpr-85676

RESUMEN

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.


Asunto(s)
Humanos , Antígeno CA-19-9/metabolismo , Carcinoma Hepatocelular/mortalidad , Colangiocarcinoma/mortalidad , Neoplasias Hepáticas/mortalidad , Imagen por Resonancia Magnética , Fenotipo , Factores de Riesgo , Análisis de Supervivencia , Tomografía Computarizada por Rayos X , alfa-Fetoproteínas/análisis
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