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A case of laryngeal leiomyosarcoma and review of the literature
Leiomyosarcoma (LMS) of the larynx is a very rare malignancy that originates from blood vessel, smooth muscle or from the heterotopic mesenchymal tissue in the larynx. The histological diagnosis of LMS depends on the immunohistochemical investigation. The case is here presented of an 82-year-old man...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772578/ https://www.ncbi.nlm.nih.gov/pubmed/26981488 http://dx.doi.org/10.4103/2231-0746.175772 |
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author | Selçuk, Ömer Tarik Renda, Levent Erol, Bekir Osma, Üstün Eyigor, Hülya Öztürk, Hülya |
author_facet | Selçuk, Ömer Tarik Renda, Levent Erol, Bekir Osma, Üstün Eyigor, Hülya Öztürk, Hülya |
author_sort | Selçuk, Ömer Tarik |
collection | PubMed |
description | Leiomyosarcoma (LMS) of the larynx is a very rare malignancy that originates from blood vessel, smooth muscle or from the heterotopic mesenchymal tissue in the larynx. The histological diagnosis of LMS depends on the immunohistochemical investigation. The case is here presented of an 82-year-old man with shortness of breath and hoarseness. Indirect laryngoscopy showed a pedunculated large glottic lesion causing airway obstruction. Direct laryngoscopy was performed and biopsies were taken. From the pathological examination, the diagnosis of LMS was made. This case is presented of laryngeal LMS with the clinical, radiological, and histological findings. |
format | Online Article Text |
id | pubmed-4772578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47725782016-03-15 A case of laryngeal leiomyosarcoma and review of the literature Selçuk, Ömer Tarik Renda, Levent Erol, Bekir Osma, Üstün Eyigor, Hülya Öztürk, Hülya Ann Maxillofac Surg Case Report - Others Leiomyosarcoma (LMS) of the larynx is a very rare malignancy that originates from blood vessel, smooth muscle or from the heterotopic mesenchymal tissue in the larynx. The histological diagnosis of LMS depends on the immunohistochemical investigation. The case is here presented of an 82-year-old man with shortness of breath and hoarseness. Indirect laryngoscopy showed a pedunculated large glottic lesion causing airway obstruction. Direct laryngoscopy was performed and biopsies were taken. From the pathological examination, the diagnosis of LMS was made. This case is presented of laryngeal LMS with the clinical, radiological, and histological findings. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4772578/ /pubmed/26981488 http://dx.doi.org/10.4103/2231-0746.175772 Text en Copyright: © 2015 Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report - Others Selçuk, Ömer Tarik Renda, Levent Erol, Bekir Osma, Üstün Eyigor, Hülya Öztürk, Hülya A case of laryngeal leiomyosarcoma and review of the literature |
title | A case of laryngeal leiomyosarcoma and review of the literature |
title_full | A case of laryngeal leiomyosarcoma and review of the literature |
title_fullStr | A case of laryngeal leiomyosarcoma and review of the literature |
title_full_unstemmed | A case of laryngeal leiomyosarcoma and review of the literature |
title_short | A case of laryngeal leiomyosarcoma and review of the literature |
title_sort | case of laryngeal leiomyosarcoma and review of the literature |
topic | Case Report - Others |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772578/ https://www.ncbi.nlm.nih.gov/pubmed/26981488 http://dx.doi.org/10.4103/2231-0746.175772 |
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