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Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description

This case describes the clinical course and treatment of a 17-year-old male patient with advanced hepatocellular carcinoma (HCC) arising in a non-cirrhotic liver. The disease was thought to be caused by a congenital cholestatic syndrome associated with intermittent oedema in childhood, resembling th...

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Autores principales: Ladekarl, Morten, Villadsen, Gerda Elisabeth, Rudbeck, Anne Roed, Aagenæs, Øystein, Nielsen, Jens Erik, Hamilton-Dutoit, Stephen, Nordsmark, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617980/
https://www.ncbi.nlm.nih.gov/pubmed/23626552
http://dx.doi.org/10.1159/000348715
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author Ladekarl, Morten
Villadsen, Gerda Elisabeth
Rudbeck, Anne Roed
Aagenæs, Øystein
Nielsen, Jens Erik
Hamilton-Dutoit, Stephen
Nordsmark, Marianne
author_facet Ladekarl, Morten
Villadsen, Gerda Elisabeth
Rudbeck, Anne Roed
Aagenæs, Øystein
Nielsen, Jens Erik
Hamilton-Dutoit, Stephen
Nordsmark, Marianne
author_sort Ladekarl, Morten
collection PubMed
description This case describes the clinical course and treatment of a 17-year-old male patient with advanced hepatocellular carcinoma (HCC) arising in a non-cirrhotic liver. The disease was thought to be caused by a congenital cholestatic syndrome associated with intermittent oedema in childhood, resembling the rare Aagenaes syndrome. Treatment choices in advanced HCC arising in adolescence are discussed.
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spelling pubmed-36179802013-04-26 Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description Ladekarl, Morten Villadsen, Gerda Elisabeth Rudbeck, Anne Roed Aagenæs, Øystein Nielsen, Jens Erik Hamilton-Dutoit, Stephen Nordsmark, Marianne Case Rep Oncol Published online: February, 2013 This case describes the clinical course and treatment of a 17-year-old male patient with advanced hepatocellular carcinoma (HCC) arising in a non-cirrhotic liver. The disease was thought to be caused by a congenital cholestatic syndrome associated with intermittent oedema in childhood, resembling the rare Aagenaes syndrome. Treatment choices in advanced HCC arising in adolescence are discussed. S. Karger AG 2013-02-19 /pmc/articles/PMC3617980/ /pubmed/23626552 http://dx.doi.org/10.1159/000348715 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No-Derivative-Works License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: February, 2013
Ladekarl, Morten
Villadsen, Gerda Elisabeth
Rudbeck, Anne Roed
Aagenæs, Øystein
Nielsen, Jens Erik
Hamilton-Dutoit, Stephen
Nordsmark, Marianne
Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title_full Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title_fullStr Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title_full_unstemmed Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title_short Advanced Hepatocellular Carcinoma in Adolescence Associated with Congenital Cholestasis: A Case Description
title_sort advanced hepatocellular carcinoma in adolescence associated with congenital cholestasis: a case description
topic Published online: February, 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617980/
https://www.ncbi.nlm.nih.gov/pubmed/23626552
http://dx.doi.org/10.1159/000348715
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