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Primary neuroendocrine tumour of the breast: a case report and review of the literature

Primary neuroendocrine tumour of the breast is a rare entity that first appeared in the 2003 World Health Organisation (WHO) classification of breast tumours. The data currently available on its prognosis are contradictory, although it seems clear that histological varieties such as small cell neuro...

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Autores principales: Tato-Varela, Sara, Albalat-Fernández, Rosa, Pabón-Fernández, Sara, Zarco, Enrique Rodríguez, Calle-Marcos, Manolo La
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720495/
https://www.ncbi.nlm.nih.gov/pubmed/26798407
http://dx.doi.org/10.3332/ecancer.2015.607
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author Tato-Varela, Sara
Albalat-Fernández, Rosa
Pabón-Fernández, Sara
Zarco, Enrique Rodríguez
Calle-Marcos, Manolo La
author_facet Tato-Varela, Sara
Albalat-Fernández, Rosa
Pabón-Fernández, Sara
Zarco, Enrique Rodríguez
Calle-Marcos, Manolo La
author_sort Tato-Varela, Sara
collection PubMed
description Primary neuroendocrine tumour of the breast is a rare entity that first appeared in the 2003 World Health Organisation (WHO) classification of breast tumours. The data currently available on its prognosis are contradictory, although it seems clear that histological varieties such as small cell neuroendocrine carcinoma have a worse prognosis, due to their low degree of differentiation. The treatment of choice is surgery, and the indications for chemotherapy or radiotherapy do not differ greatly from those used for other breast tumours. It is crucial to underline the difficulty of establishing treatment protocols due to the low incidence of this histological type.
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spelling pubmed-47204952016-01-21 Primary neuroendocrine tumour of the breast: a case report and review of the literature Tato-Varela, Sara Albalat-Fernández, Rosa Pabón-Fernández, Sara Zarco, Enrique Rodríguez Calle-Marcos, Manolo La Ecancermedicalscience Case Report Primary neuroendocrine tumour of the breast is a rare entity that first appeared in the 2003 World Health Organisation (WHO) classification of breast tumours. The data currently available on its prognosis are contradictory, although it seems clear that histological varieties such as small cell neuroendocrine carcinoma have a worse prognosis, due to their low degree of differentiation. The treatment of choice is surgery, and the indications for chemotherapy or radiotherapy do not differ greatly from those used for other breast tumours. It is crucial to underline the difficulty of establishing treatment protocols due to the low incidence of this histological type. Cancer Intelligence 2015-12-22 /pmc/articles/PMC4720495/ /pubmed/26798407 http://dx.doi.org/10.3332/ecancer.2015.607 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
Zarco, Enrique Rodríguez
Calle-Marcos, Manolo La
Primary neuroendocrine tumour of the breast: a case report and review of the literature
title Primary neuroendocrine tumour of the breast: a case report and review of the literature
title_full Primary neuroendocrine tumour of the breast: a case report and review of the literature
title_fullStr Primary neuroendocrine tumour of the breast: a case report and review of the literature
title_full_unstemmed Primary neuroendocrine tumour of the breast: a case report and review of the literature
title_short Primary neuroendocrine tumour of the breast: a case report and review of the literature
title_sort primary neuroendocrine tumour of the breast: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720495/
https://www.ncbi.nlm.nih.gov/pubmed/26798407
http://dx.doi.org/10.3332/ecancer.2015.607
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