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Laryngeal chondrosarcoma – Ten years of experience()
INTRODUCTION: Laryngeal involvement by cartilaginous tumors is rare. However, although accounting for only 1% of laryngeal tumor pathology, they are the most frequently occurring non-epithelial neoplasms. The most probable location is the endolaryngeal surface of the cricoid cartilage. Their symptom...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444598/ https://www.ncbi.nlm.nih.gov/pubmed/25183187 http://dx.doi.org/10.1016/j.bjorl.2014.05.004 |
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author | Oliveira, José Fernando dos Santos Branquinho, Francisco António Pinto Lopes Monteiro, Ana Rita Raposeiro Tomé Nobre Portugal, Maria Edite Correia Castro Guimarães, Arnaldo Manuel Ferreira Silva |
author_facet | Oliveira, José Fernando dos Santos Branquinho, Francisco António Pinto Lopes Monteiro, Ana Rita Raposeiro Tomé Nobre Portugal, Maria Edite Correia Castro Guimarães, Arnaldo Manuel Ferreira Silva |
author_sort | Oliveira, José Fernando dos Santos |
collection | PubMed |
description | INTRODUCTION: Laryngeal involvement by cartilaginous tumors is rare. However, although accounting for only 1% of laryngeal tumor pathology, they are the most frequently occurring non-epithelial neoplasms. The most probable location is the endolaryngeal surface of the cricoid cartilage. Their symptoms are variable, depending on the size and location, and may include hoarseness, stridor, and dyspnea. Treatment is based on surgical excision. Some centers take into account the degree of differentiation and whether it is a case of relapse when deciding to perform a radical resection. AIM: To evaluate this disease in a sample of the Portuguese population. METHODS: A review of the medical records from 2002 to 2012 by assessment of clinical processes was performed. Data on demographics, clinical treatments, and outcomes were collected. RESULTS: Six patients were included in the study. Five of them underwent total laryngectomy, and in one case, partial excision of the thyroid cartilage was performed. None of the patients had either metastases or tumor-related death. CONCLUSION: Laryngeal chondrosarcomas remain a rare disease of unknown etiology, with slow and insidious symptoms. The treatment is surgical, with favorable prognosis, and metastases rarely occur. The main concern regards their propensity to relapse. |
format | Online Article Text |
id | pubmed-9444598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94445982022-09-09 Laryngeal chondrosarcoma – Ten years of experience() Oliveira, José Fernando dos Santos Branquinho, Francisco António Pinto Lopes Monteiro, Ana Rita Raposeiro Tomé Nobre Portugal, Maria Edite Correia Castro Guimarães, Arnaldo Manuel Ferreira Silva Braz J Otorhinolaryngol Review Article INTRODUCTION: Laryngeal involvement by cartilaginous tumors is rare. However, although accounting for only 1% of laryngeal tumor pathology, they are the most frequently occurring non-epithelial neoplasms. The most probable location is the endolaryngeal surface of the cricoid cartilage. Their symptoms are variable, depending on the size and location, and may include hoarseness, stridor, and dyspnea. Treatment is based on surgical excision. Some centers take into account the degree of differentiation and whether it is a case of relapse when deciding to perform a radical resection. AIM: To evaluate this disease in a sample of the Portuguese population. METHODS: A review of the medical records from 2002 to 2012 by assessment of clinical processes was performed. Data on demographics, clinical treatments, and outcomes were collected. RESULTS: Six patients were included in the study. Five of them underwent total laryngectomy, and in one case, partial excision of the thyroid cartilage was performed. None of the patients had either metastases or tumor-related death. CONCLUSION: Laryngeal chondrosarcomas remain a rare disease of unknown etiology, with slow and insidious symptoms. The treatment is surgical, with favorable prognosis, and metastases rarely occur. The main concern regards their propensity to relapse. Elsevier 2014-05-27 /pmc/articles/PMC9444598/ /pubmed/25183187 http://dx.doi.org/10.1016/j.bjorl.2014.05.004 Text en © 2014 Associac¸ão Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Published by Elsevier Editora Ltda. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Review Article Oliveira, José Fernando dos Santos Branquinho, Francisco António Pinto Lopes Monteiro, Ana Rita Raposeiro Tomé Nobre Portugal, Maria Edite Correia Castro Guimarães, Arnaldo Manuel Ferreira Silva Laryngeal chondrosarcoma – Ten years of experience() |
title | Laryngeal chondrosarcoma – Ten years of experience() |
title_full | Laryngeal chondrosarcoma – Ten years of experience() |
title_fullStr | Laryngeal chondrosarcoma – Ten years of experience() |
title_full_unstemmed | Laryngeal chondrosarcoma – Ten years of experience() |
title_short | Laryngeal chondrosarcoma – Ten years of experience() |
title_sort | laryngeal chondrosarcoma – ten years of experience() |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444598/ https://www.ncbi.nlm.nih.gov/pubmed/25183187 http://dx.doi.org/10.1016/j.bjorl.2014.05.004 |
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