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Laryngeal Leiomyosarcoma, A Case Report and Review of Articles

INTRODUCTION: Laryngeal leiomysarcoma is an extremely rare malignancy originating from smooth muscle cells. Its rarity is due to the fact that only less than 50 cases of pure laryngeal leiomyosarcoma and less than 10 cases of hypopharyngeal leiomyosarcaoma have been reported in modern medical litera...

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Autores principales: Khadivi, Ehsan, Taziky, Mohammad Hossein, Jafarian, Amir Hossein, Nasseri Sadr, Msoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846253/
https://www.ncbi.nlm.nih.gov/pubmed/24303449
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author Khadivi, Ehsan
Taziky, Mohammad Hossein
Jafarian, Amir Hossein
Nasseri Sadr, Msoud
author_facet Khadivi, Ehsan
Taziky, Mohammad Hossein
Jafarian, Amir Hossein
Nasseri Sadr, Msoud
author_sort Khadivi, Ehsan
collection PubMed
description INTRODUCTION: Laryngeal leiomysarcoma is an extremely rare malignancy originating from smooth muscle cells. Its rarity is due to the fact that only less than 50 cases of pure laryngeal leiomyosarcoma and less than 10 cases of hypopharyngeal leiomyosarcaoma have been reported in modern medical literature. Even though the clinical presentation mimics that of a laryngeal carcinoma forming the major bulk of the laryngeal malignancies, the difference in management, warrants an accurate diagnosis. CASE REPORT: We reported a case of this very rare malignancy presenting in the supraglottic region by highlighting the clinical features, histological and radiological diagnosis and management of this extremely rare malignant entity. CONCLUSION: An accurate histological diagnosis may be difficult; but supplementing by electron microscopy and immunohistochemical staining, the diagnosis can be reached certainly.
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spelling pubmed-38462532013-12-03 Laryngeal Leiomyosarcoma, A Case Report and Review of Articles Khadivi, Ehsan Taziky, Mohammad Hossein Jafarian, Amir Hossein Nasseri Sadr, Msoud Iran J Otorhinolaryngol Case Report INTRODUCTION: Laryngeal leiomysarcoma is an extremely rare malignancy originating from smooth muscle cells. Its rarity is due to the fact that only less than 50 cases of pure laryngeal leiomyosarcoma and less than 10 cases of hypopharyngeal leiomyosarcaoma have been reported in modern medical literature. Even though the clinical presentation mimics that of a laryngeal carcinoma forming the major bulk of the laryngeal malignancies, the difference in management, warrants an accurate diagnosis. CASE REPORT: We reported a case of this very rare malignancy presenting in the supraglottic region by highlighting the clinical features, histological and radiological diagnosis and management of this extremely rare malignant entity. CONCLUSION: An accurate histological diagnosis may be difficult; but supplementing by electron microscopy and immunohistochemical staining, the diagnosis can be reached certainly. Mashhad University of Medical Sciences 2013-10 /pmc/articles/PMC3846253/ /pubmed/24303449 Text en © 2013: Iranian Journal of Otorhinolaryngology 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
Khadivi, Ehsan
Taziky, Mohammad Hossein
Jafarian, Amir Hossein
Nasseri Sadr, Msoud
Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title_full Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title_fullStr Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title_full_unstemmed Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title_short Laryngeal Leiomyosarcoma, A Case Report and Review of Articles
title_sort laryngeal leiomyosarcoma, a case report and review of articles
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846253/
https://www.ncbi.nlm.nih.gov/pubmed/24303449
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