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Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree

An endobronchial leiomyoma is a rare tumor of the bronchial tree. Very few cases have been reported in literature. Leiomyomas account for less than 2% of all benign lung tumors. Only one third is endobronchial in location, usually presenting as primary solitary lesions and airway obstruction finding...

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Detalles Bibliográficos
Autores principales: Swarnakar, Rajesh, Sinha, Sheetal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644836/
https://www.ncbi.nlm.nih.gov/pubmed/23661918
http://dx.doi.org/10.4103/0970-2113.106175
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author Swarnakar, Rajesh
Sinha, Sheetal
author_facet Swarnakar, Rajesh
Sinha, Sheetal
author_sort Swarnakar, Rajesh
collection PubMed
description An endobronchial leiomyoma is a rare tumor of the bronchial tree. Very few cases have been reported in literature. Leiomyomas account for less than 2% of all benign lung tumors. Only one third is endobronchial in location, usually presenting as primary solitary lesions and airway obstruction findings. Literature on primary endobronchial leiomyomas is therefore scarce, with a few more than 100 cases being reported. These tumors arise from the smooth muscle of the bronchial tree. Symptomatology is based on the degree of endoluminal bronchial obstruction and surgical resection has generally been the mainstay of treatment. We describe a case of endobronchial leiomyoma in a 42 year old female. A diagnosis of Primary endobronchial leiomyoma was made on the basis of histopathology and immunohistochemistry. Rarity of this tumor in the bronchial tree with coexisting interstitial peumonitis urges us to report this case.
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spelling pubmed-36448362013-05-09 Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree Swarnakar, Rajesh Sinha, Sheetal Lung India Case Report An endobronchial leiomyoma is a rare tumor of the bronchial tree. Very few cases have been reported in literature. Leiomyomas account for less than 2% of all benign lung tumors. Only one third is endobronchial in location, usually presenting as primary solitary lesions and airway obstruction findings. Literature on primary endobronchial leiomyomas is therefore scarce, with a few more than 100 cases being reported. These tumors arise from the smooth muscle of the bronchial tree. Symptomatology is based on the degree of endoluminal bronchial obstruction and surgical resection has generally been the mainstay of treatment. We describe a case of endobronchial leiomyoma in a 42 year old female. A diagnosis of Primary endobronchial leiomyoma was made on the basis of histopathology and immunohistochemistry. Rarity of this tumor in the bronchial tree with coexisting interstitial peumonitis urges us to report this case. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3644836/ /pubmed/23661918 http://dx.doi.org/10.4103/0970-2113.106175 Text en Copyright: © Lung India 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Swarnakar, Rajesh
Sinha, Sheetal
Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title_full Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title_fullStr Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title_full_unstemmed Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title_short Endobronchial leiomyoma: A rare and innocent tumour of the bronchial tree
title_sort endobronchial leiomyoma: a rare and innocent tumour of the bronchial tree
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644836/
https://www.ncbi.nlm.nih.gov/pubmed/23661918
http://dx.doi.org/10.4103/0970-2113.106175
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