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De-novo hepatocellular carcinoma after pediatric living donor liver transplantation

De-novo malignancies carry an incidence ranging between 3%-26% after transplant and account for the second highest cause of post-transplant mortality behind cardiovascular disease. While the majority of de-novo malignancies after transplant usually consist of skin cancers, there has been an increasi...

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Autores principales: Torres-Landa, Samuel, Muñoz-Abraham, Armando Salim, Fortune, Brett E, Gurung, Ananta, Pollak, Jeffrey, Emre, Sukru H, Rodriguez-Davalos, Manuel I, Schilsky, Michael L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756726/
https://www.ncbi.nlm.nih.gov/pubmed/29359020
http://dx.doi.org/10.4254/wjh.v9.i36.1361
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author Torres-Landa, Samuel
Muñoz-Abraham, Armando Salim
Fortune, Brett E
Gurung, Ananta
Pollak, Jeffrey
Emre, Sukru H
Rodriguez-Davalos, Manuel I
Schilsky, Michael L
author_facet Torres-Landa, Samuel
Muñoz-Abraham, Armando Salim
Fortune, Brett E
Gurung, Ananta
Pollak, Jeffrey
Emre, Sukru H
Rodriguez-Davalos, Manuel I
Schilsky, Michael L
author_sort Torres-Landa, Samuel
collection PubMed
description De-novo malignancies carry an incidence ranging between 3%-26% after transplant and account for the second highest cause of post-transplant mortality behind cardiovascular disease. While the majority of de-novo malignancies after transplant usually consist of skin cancers, there has been an increasing rate of solid tumor cancers over the last 15 years. Although, recurrence of hepatocellular carcinoma (HCC) is well understood among patients transplanted for HCC, there are increasing reports of de-novo HCC in those transplanted for a non-HCC indication. The proposed pathophysiology for these cases has been mainly connected to the presence of advanced graft fibrosis or cirrhosis and always associated with the presence of hepatitis B or C virus. We report the first known case of de-novo HCC in a recipient, 14 years after a pediatric living related donor liver transplantation for end-stage liver disease due to biliary atresia without the presence of hepatitis B or C virus before and after transplant. We present this case report to increase the awareness of this phenomenon and address on the utility for screening and surveillance of hepatocellular carcinoma among these individuals. One recommendation is to use similar guidelines for screening, diagnosis, and treatment for HCC as those used for primary HCC in the pre-transplant patient, focusing on those recipients who have advanced fibrosis in the allograft, regardless of etiology.
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spelling pubmed-57567262018-01-22 De-novo hepatocellular carcinoma after pediatric living donor liver transplantation Torres-Landa, Samuel Muñoz-Abraham, Armando Salim Fortune, Brett E Gurung, Ananta Pollak, Jeffrey Emre, Sukru H Rodriguez-Davalos, Manuel I Schilsky, Michael L World J Hepatol Case Report De-novo malignancies carry an incidence ranging between 3%-26% after transplant and account for the second highest cause of post-transplant mortality behind cardiovascular disease. While the majority of de-novo malignancies after transplant usually consist of skin cancers, there has been an increasing rate of solid tumor cancers over the last 15 years. Although, recurrence of hepatocellular carcinoma (HCC) is well understood among patients transplanted for HCC, there are increasing reports of de-novo HCC in those transplanted for a non-HCC indication. The proposed pathophysiology for these cases has been mainly connected to the presence of advanced graft fibrosis or cirrhosis and always associated with the presence of hepatitis B or C virus. We report the first known case of de-novo HCC in a recipient, 14 years after a pediatric living related donor liver transplantation for end-stage liver disease due to biliary atresia without the presence of hepatitis B or C virus before and after transplant. We present this case report to increase the awareness of this phenomenon and address on the utility for screening and surveillance of hepatocellular carcinoma among these individuals. One recommendation is to use similar guidelines for screening, diagnosis, and treatment for HCC as those used for primary HCC in the pre-transplant patient, focusing on those recipients who have advanced fibrosis in the allograft, regardless of etiology. Baishideng Publishing Group Inc 2017-12-28 2017-12-28 /pmc/articles/PMC5756726/ /pubmed/29359020 http://dx.doi.org/10.4254/wjh.v9.i36.1361 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Torres-Landa, Samuel
Muñoz-Abraham, Armando Salim
Fortune, Brett E
Gurung, Ananta
Pollak, Jeffrey
Emre, Sukru H
Rodriguez-Davalos, Manuel I
Schilsky, Michael L
De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title_full De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title_fullStr De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title_full_unstemmed De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title_short De-novo hepatocellular carcinoma after pediatric living donor liver transplantation
title_sort de-novo hepatocellular carcinoma after pediatric living donor liver transplantation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756726/
https://www.ncbi.nlm.nih.gov/pubmed/29359020
http://dx.doi.org/10.4254/wjh.v9.i36.1361
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