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Hyperplastic Cardiac Sarcoma Recurrence

Primary cardiac sarcomas are rare tumors with a median survival of 6–12 months. Data suggest that an aggressive multidisciplinary approach may improve patient outcome. We present the case of a male who underwent resection of cardiac sarcoma three times from the age of 32 to 34. This report discusses...

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Autores principales: Shariff, Masood A., Abreu, Juan A., Durrani, Farida, Daniele, Eddie, Bowman, Kimberly C., Sadel, Scott, Asgarian, Kourosh T., McGinn, Joseph T., Nabagiez, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377465/
https://www.ncbi.nlm.nih.gov/pubmed/25861508
http://dx.doi.org/10.1155/2015/132328
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author Shariff, Masood A.
Abreu, Juan A.
Durrani, Farida
Daniele, Eddie
Bowman, Kimberly C.
Sadel, Scott
Asgarian, Kourosh T.
McGinn, Joseph T.
Nabagiez, John P.
author_facet Shariff, Masood A.
Abreu, Juan A.
Durrani, Farida
Daniele, Eddie
Bowman, Kimberly C.
Sadel, Scott
Asgarian, Kourosh T.
McGinn, Joseph T.
Nabagiez, John P.
author_sort Shariff, Masood A.
collection PubMed
description Primary cardiac sarcomas are rare tumors with a median survival of 6–12 months. Data suggest that an aggressive multidisciplinary approach may improve patient outcome. We present the case of a male who underwent resection of cardiac sarcoma three times from the age of 32 to 34. This report discusses the malignant nature of cardiac sarcoma and the importance of postoperative multidisciplinary care.
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spelling pubmed-43774652015-04-08 Hyperplastic Cardiac Sarcoma Recurrence Shariff, Masood A. Abreu, Juan A. Durrani, Farida Daniele, Eddie Bowman, Kimberly C. Sadel, Scott Asgarian, Kourosh T. McGinn, Joseph T. Nabagiez, John P. Case Rep Surg Case Report Primary cardiac sarcomas are rare tumors with a median survival of 6–12 months. Data suggest that an aggressive multidisciplinary approach may improve patient outcome. We present the case of a male who underwent resection of cardiac sarcoma three times from the age of 32 to 34. This report discusses the malignant nature of cardiac sarcoma and the importance of postoperative multidisciplinary care. Hindawi Publishing Corporation 2015 2015-02-15 /pmc/articles/PMC4377465/ /pubmed/25861508 http://dx.doi.org/10.1155/2015/132328 Text en Copyright © 2015 Masood A. Shariff 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
Shariff, Masood A.
Abreu, Juan A.
Durrani, Farida
Daniele, Eddie
Bowman, Kimberly C.
Sadel, Scott
Asgarian, Kourosh T.
McGinn, Joseph T.
Nabagiez, John P.
Hyperplastic Cardiac Sarcoma Recurrence
title Hyperplastic Cardiac Sarcoma Recurrence
title_full Hyperplastic Cardiac Sarcoma Recurrence
title_fullStr Hyperplastic Cardiac Sarcoma Recurrence
title_full_unstemmed Hyperplastic Cardiac Sarcoma Recurrence
title_short Hyperplastic Cardiac Sarcoma Recurrence
title_sort hyperplastic cardiac sarcoma recurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377465/
https://www.ncbi.nlm.nih.gov/pubmed/25861508
http://dx.doi.org/10.1155/2015/132328
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