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Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions

Combined hepatocellular cholangiocarcinoma (CC) is a rare and aggressive primary hepatic malignancy with significant histological and biological heterogeneity. It presents with more aggressive behavior and worse survival outcomes than either hepatocellular carcinoma or CC and remains a diagnostic ch...

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Detalles Bibliográficos
Autores principales: Stavraka, Chara, Rush, Hannah, Ross, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312394/
https://www.ncbi.nlm.nih.gov/pubmed/30643759
http://dx.doi.org/10.2147/JHC.S159805
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author Stavraka, Chara
Rush, Hannah
Ross, Paul
author_facet Stavraka, Chara
Rush, Hannah
Ross, Paul
author_sort Stavraka, Chara
collection PubMed
description Combined hepatocellular cholangiocarcinoma (CC) is a rare and aggressive primary hepatic malignancy with significant histological and biological heterogeneity. It presents with more aggressive behavior and worse survival outcomes than either hepatocellular carcinoma or CC and remains a diagnostic challenge. An accurate diagnosis is crucial for its optimal management. Major hepatectomy with hilar node resection remains the mainstay of treatment in operable cases. Advances in the genetic and molecular characterization of this tumor will contribute to the better understanding of its pathogenesis and shape its future management.
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spelling pubmed-63123942019-01-14 Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions Stavraka, Chara Rush, Hannah Ross, Paul J Hepatocell Carcinoma Review Combined hepatocellular cholangiocarcinoma (CC) is a rare and aggressive primary hepatic malignancy with significant histological and biological heterogeneity. It presents with more aggressive behavior and worse survival outcomes than either hepatocellular carcinoma or CC and remains a diagnostic challenge. An accurate diagnosis is crucial for its optimal management. Major hepatectomy with hilar node resection remains the mainstay of treatment in operable cases. Advances in the genetic and molecular characterization of this tumor will contribute to the better understanding of its pathogenesis and shape its future management. Dove Medical Press 2018-12-28 /pmc/articles/PMC6312394/ /pubmed/30643759 http://dx.doi.org/10.2147/JHC.S159805 Text en © 2019 Stavraka et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Stavraka, Chara
Rush, Hannah
Ross, Paul
Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title_full Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title_fullStr Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title_full_unstemmed Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title_short Combined hepatocellular cholangiocarcinoma (cHCC-CC): an update of genetics, molecular biology, and therapeutic interventions
title_sort combined hepatocellular cholangiocarcinoma (chcc-cc): an update of genetics, molecular biology, and therapeutic interventions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312394/
https://www.ncbi.nlm.nih.gov/pubmed/30643759
http://dx.doi.org/10.2147/JHC.S159805
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