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Autor:
Ajacio Bandeira de Mello, Brandão, Santiago, Rodriguez, Alfeu de Medeiros, Fleck, Claudio Augusto, Marroni, Mário B, Wagner, Alex, Hörbe, Matheus V, Fernandes, Carlos Ts, Cerski, Gabriela Perdomo, Coral
Publikováno v:
World Journal of Clinical Oncology. 13:688-701
Cholangiocarcinoma (CC) is a rare tumor that arises from the epithelium of the bile ducts. It is classified according to anatomic location as intrahepatic, perihilar, and distal. Intrahepatic CC (ICC) is rare in patients with cirrhosis due to causes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c71fbea86f9ba6d6dbfabf08908172
https://doi.org/10.5306/wjco.v13.i8.688
https://doi.org/10.5306/wjco.v13.i8.688
