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.
| Original language | English |
|---|---|
| Pages (from-to) | 406-410 |
| Number of pages | 5 |
| Journal | Clinical and Molecular Hepatology |
| Volume | 20 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1 Dec 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Bi-phenotypic tumors
- Cholangiocarcinoma
- Computed tomography, Magnetic resonance imaging
- Hepatoceullular carcinoma
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