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Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report

Small cell neuroendocrine carcinoma rarely appears primarily in the head and neck and exhibits aggressive behavior with a poor prognosis. The pathologist has a significant role in the diagnosis, and a consensual treatment still does not exist. The authors report the case of a middle-aged male patien...

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Autores principales: Azevedo, Daniela, Rios, Elisabete, Vendeira, Lurdes, Sarmento, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436919/
https://www.ncbi.nlm.nih.gov/pubmed/28536685
http://dx.doi.org/10.4322/acr.2017.002
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author Azevedo, Daniela
Rios, Elisabete
Vendeira, Lurdes
Sarmento, Cristina
author_facet Azevedo, Daniela
Rios, Elisabete
Vendeira, Lurdes
Sarmento, Cristina
author_sort Azevedo, Daniela
collection PubMed
description Small cell neuroendocrine carcinoma rarely appears primarily in the head and neck and exhibits aggressive behavior with a poor prognosis. The pathologist has a significant role in the diagnosis, and a consensual treatment still does not exist. The authors report the case of a middle-aged male patient who presented repeated episodes of massive epistaxis. The diagnostic work-up disclosed the diagnosis of small cell neuroendocrine carcinoma of the nasopharynx. The patient was treated with chemotherapy followed by radiotherapy. Imaging examinations performed after the end of treatment showed apparent complete remission of the disease. The patient was kept under active surveillance with no signs of local relapse or distant metastasis after 4 years of follow-up.
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spelling pubmed-54369192017-05-23 Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report Azevedo, Daniela Rios, Elisabete Vendeira, Lurdes Sarmento, Cristina Autops Case Rep Article / Clinical Case Report Small cell neuroendocrine carcinoma rarely appears primarily in the head and neck and exhibits aggressive behavior with a poor prognosis. The pathologist has a significant role in the diagnosis, and a consensual treatment still does not exist. The authors report the case of a middle-aged male patient who presented repeated episodes of massive epistaxis. The diagnostic work-up disclosed the diagnosis of small cell neuroendocrine carcinoma of the nasopharynx. The patient was treated with chemotherapy followed by radiotherapy. Imaging examinations performed after the end of treatment showed apparent complete remission of the disease. The patient was kept under active surveillance with no signs of local relapse or distant metastasis after 4 years of follow-up. São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2017-03-30 /pmc/articles/PMC5436919/ /pubmed/28536685 http://dx.doi.org/10.4322/acr.2017.002 Text en Autopsy and Case Reports. ISSN 2236-1960. Copyright © 2017. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the article is properly cited.
spellingShingle Article / Clinical Case Report
Azevedo, Daniela
Rios, Elisabete
Vendeira, Lurdes
Sarmento, Cristina
Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title_full Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title_fullStr Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title_full_unstemmed Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title_short Small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
title_sort small cell neuroendocrine carcinoma of the nasopharynx: a rare case report
topic Article / Clinical Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436919/
https://www.ncbi.nlm.nih.gov/pubmed/28536685
http://dx.doi.org/10.4322/acr.2017.002
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