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Radiation-induced breast angiosarcoma: a case report

Radiation-induced breast angiosarcoma is a severe but rare late complication in the breast-preserving management of breast cancer through surgery and radiotherapy [1]. Often the initial diagnosis of this entity is complex given its relatively anodyne nature and usually being present in the form of t...

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Autores principales: Tato-Varela, Sara, Albalat-Fernández, Rosa, Pabón-Fernández, Sara, Núñez-García, Diego, Calle-Marcos, Manolo La
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215290/
https://www.ncbi.nlm.nih.gov/pubmed/28101140
http://dx.doi.org/10.3332/ecancer.2016.697
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author Tato-Varela, Sara
Albalat-Fernández, Rosa
Pabón-Fernández, Sara
Núñez-García, Diego
Calle-Marcos, Manolo La
author_facet Tato-Varela, Sara
Albalat-Fernández, Rosa
Pabón-Fernández, Sara
Núñez-García, Diego
Calle-Marcos, Manolo La
author_sort Tato-Varela, Sara
collection PubMed
description Radiation-induced breast angiosarcoma is a severe but rare late complication in the breast-preserving management of breast cancer through surgery and radiotherapy [1]. Often the initial diagnosis of this entity is complex given its relatively anodyne nature and usually being present in the form of typically multifocal reddish-purple papular skin lesions [2]. Because of the low incidence of this tumour, there is a limited number of studies regarding its optimal therapeutic management [3]. The preferred treatment is aggressive surgical removal and the prognosis is poor with an overall survival rate of 12–20% at five years [4].
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spelling pubmed-52152902017-01-18 Radiation-induced breast angiosarcoma: a case report Tato-Varela, Sara Albalat-Fernández, Rosa Pabón-Fernández, Sara Núñez-García, Diego Calle-Marcos, Manolo La Ecancermedicalscience Case Report Radiation-induced breast angiosarcoma is a severe but rare late complication in the breast-preserving management of breast cancer through surgery and radiotherapy [1]. Often the initial diagnosis of this entity is complex given its relatively anodyne nature and usually being present in the form of typically multifocal reddish-purple papular skin lesions [2]. Because of the low incidence of this tumour, there is a limited number of studies regarding its optimal therapeutic management [3]. The preferred treatment is aggressive surgical removal and the prognosis is poor with an overall survival rate of 12–20% at five years [4]. Cancer Intelligence 2016-11-29 /pmc/articles/PMC5215290/ /pubmed/28101140 http://dx.doi.org/10.3332/ecancer.2016.697 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tato-Varela, Sara
Albalat-Fernández, Rosa
Pabón-Fernández, Sara
Núñez-García, Diego
Calle-Marcos, Manolo La
Radiation-induced breast angiosarcoma: a case report
title Radiation-induced breast angiosarcoma: a case report
title_full Radiation-induced breast angiosarcoma: a case report
title_fullStr Radiation-induced breast angiosarcoma: a case report
title_full_unstemmed Radiation-induced breast angiosarcoma: a case report
title_short Radiation-induced breast angiosarcoma: a case report
title_sort radiation-induced breast angiosarcoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215290/
https://www.ncbi.nlm.nih.gov/pubmed/28101140
http://dx.doi.org/10.3332/ecancer.2016.697
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