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Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis

Primary hepatic carcinoids are rare tumors that are often diagnosed at a locally advanced stage. Their primary nature can only be ascertained after thorough investigations and long-term follow-up to exclude another primary origin. As with secondary neuroendocrine liver tumors, surgical resection rem...

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Autores principales: Landen, Serge, Elens, Maxime, Vrancken, Celine, Nuytens, Frederiek, Meert, Thibault, Delugeau, Veronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932648/
https://www.ncbi.nlm.nih.gov/pubmed/24653852
http://dx.doi.org/10.1155/2014/456509
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author Landen, Serge
Elens, Maxime
Vrancken, Celine
Nuytens, Frederiek
Meert, Thibault
Delugeau, Veronique
author_facet Landen, Serge
Elens, Maxime
Vrancken, Celine
Nuytens, Frederiek
Meert, Thibault
Delugeau, Veronique
author_sort Landen, Serge
collection PubMed
description Primary hepatic carcinoids are rare tumors that are often diagnosed at a locally advanced stage. Their primary nature can only be ascertained after thorough investigations and long-term follow-up to exclude another primary origin. As with secondary neuroendocrine liver tumors, surgical resection remains the mainstay of therapy. Despite their large size and often central location liver resection is often feasible, offering long-term survival and cure to most patients. In selected patients liver transplantation appears to be a good indication for tumors not amenable to liver resection. An aggressive surgical attitude is therefore warranted. We report a large and unusually fast-growing liver carcinoid that appeared only marginally resectable in a patient who remains free of disease four years after surgery.
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spelling pubmed-39326482014-03-20 Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis Landen, Serge Elens, Maxime Vrancken, Celine Nuytens, Frederiek Meert, Thibault Delugeau, Veronique Case Rep Surg Case Report Primary hepatic carcinoids are rare tumors that are often diagnosed at a locally advanced stage. Their primary nature can only be ascertained after thorough investigations and long-term follow-up to exclude another primary origin. As with secondary neuroendocrine liver tumors, surgical resection remains the mainstay of therapy. Despite their large size and often central location liver resection is often feasible, offering long-term survival and cure to most patients. In selected patients liver transplantation appears to be a good indication for tumors not amenable to liver resection. An aggressive surgical attitude is therefore warranted. We report a large and unusually fast-growing liver carcinoid that appeared only marginally resectable in a patient who remains free of disease four years after surgery. Hindawi Publishing Corporation 2014 2014-02-09 /pmc/articles/PMC3932648/ /pubmed/24653852 http://dx.doi.org/10.1155/2014/456509 Text en Copyright © 2014 Serge Landen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Landen, Serge
Elens, Maxime
Vrancken, Celine
Nuytens, Frederiek
Meert, Thibault
Delugeau, Veronique
Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title_full Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title_fullStr Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title_full_unstemmed Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title_short Giant Hepatic Carcinoid: A Rare Tumor with a Favorable Prognosis
title_sort giant hepatic carcinoid: a rare tumor with a favorable prognosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932648/
https://www.ncbi.nlm.nih.gov/pubmed/24653852
http://dx.doi.org/10.1155/2014/456509
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