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Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture

Mediastinal glomus tumors are rarely recognized, and only seven cases have been reported in the literature. Here, we describe a rare mediastinal glomus tumor and review the characteristics of this rare clinical case. The patient was a 50-year-old female who presented with coughing for 3 months. Her...

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Detalles Bibliográficos
Autores principales: Fang, Zhongjie, Ma, Dehua, Chen, Baofu, Luo, Huarong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241500/
https://www.ncbi.nlm.nih.gov/pubmed/28133561
http://dx.doi.org/10.1155/2017/3621839
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author Fang, Zhongjie
Ma, Dehua
Chen, Baofu
Luo, Huarong
author_facet Fang, Zhongjie
Ma, Dehua
Chen, Baofu
Luo, Huarong
author_sort Fang, Zhongjie
collection PubMed
description Mediastinal glomus tumors are rarely recognized, and only seven cases have been reported in the literature. Here, we describe a rare mediastinal glomus tumor and review the characteristics of this rare clinical case. The patient was a 50-year-old female who presented with coughing for 3 months. Her chest computed tomography scan demonstrated a localized tumor in the posterior superior mediastinum. Intraoperatively, we found a longitudinal rupture of the membranous trachea above the carina. We completely resected the tumor and repaired the tracheal rupture under a thoracoscopy using a pedicled muscle flap. The tissue was diagnosed as a mediastinal glomus tumor according to its histological and immunophenotypic characteristics.
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spelling pubmed-52415002017-01-29 Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture Fang, Zhongjie Ma, Dehua Chen, Baofu Luo, Huarong Case Rep Surg Case Report Mediastinal glomus tumors are rarely recognized, and only seven cases have been reported in the literature. Here, we describe a rare mediastinal glomus tumor and review the characteristics of this rare clinical case. The patient was a 50-year-old female who presented with coughing for 3 months. Her chest computed tomography scan demonstrated a localized tumor in the posterior superior mediastinum. Intraoperatively, we found a longitudinal rupture of the membranous trachea above the carina. We completely resected the tumor and repaired the tracheal rupture under a thoracoscopy using a pedicled muscle flap. The tissue was diagnosed as a mediastinal glomus tumor according to its histological and immunophenotypic characteristics. Hindawi Publishing Corporation 2017 2017-01-04 /pmc/articles/PMC5241500/ /pubmed/28133561 http://dx.doi.org/10.1155/2017/3621839 Text en Copyright © 2017 Zhongjie Fang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Fang, Zhongjie
Ma, Dehua
Chen, Baofu
Luo, Huarong
Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title_full Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title_fullStr Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title_full_unstemmed Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title_short Thoracoscopic Surgery for Glomus Tumor: An Uncommon Mediastinal Neoplasm and Iatrogenic Tracheal Rupture
title_sort thoracoscopic surgery for glomus tumor: an uncommon mediastinal neoplasm and iatrogenic tracheal rupture
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241500/
https://www.ncbi.nlm.nih.gov/pubmed/28133561
http://dx.doi.org/10.1155/2017/3621839
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