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Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection

Ortner syndrome or cardiovocal syndrome is hoarseness of voice due to left recurrent laryngeal nerve palsy as a result of cardiovascular abnormality. It is not known that pneumothorax has any association with Ortner syndrome. A 56‐year‐old gentleman, with previous history of 20 pack‐year smoking and...

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Autores principales: Lo, Shan Min, Ramarmuty, Hema Yamini, Kannan, Kunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883475/
https://www.ncbi.nlm.nih.gov/pubmed/33614038
http://dx.doi.org/10.1002/rcr2.718
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author Lo, Shan Min
Ramarmuty, Hema Yamini
Kannan, Kunji
author_facet Lo, Shan Min
Ramarmuty, Hema Yamini
Kannan, Kunji
author_sort Lo, Shan Min
collection PubMed
description Ortner syndrome or cardiovocal syndrome is hoarseness of voice due to left recurrent laryngeal nerve palsy as a result of cardiovascular abnormality. It is not known that pneumothorax has any association with Ortner syndrome. A 56‐year‐old gentleman, with previous history of 20 pack‐year smoking and 1‐year history of hypertension, presented to us with cough for two weeks with intermittent haemoptysis, as well as hoarseness of voice for the past one year. Direct laryngoscopy confirmed that he had left vocal cord palsy. Clinical and radiological investigations suggested that he had left pneumothorax. Left chest tube thoracostomy was performed and computed tomography of chest revealed aortic isthmus aneurysm with dissection extending to distal left common iliac artery and residual left hydropneumothorax. The patient was then referred to the vascular team and cardiothoracic team for further management.
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spelling pubmed-78834752021-02-19 Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection Lo, Shan Min Ramarmuty, Hema Yamini Kannan, Kunji Respirol Case Rep Case Reports Ortner syndrome or cardiovocal syndrome is hoarseness of voice due to left recurrent laryngeal nerve palsy as a result of cardiovascular abnormality. It is not known that pneumothorax has any association with Ortner syndrome. A 56‐year‐old gentleman, with previous history of 20 pack‐year smoking and 1‐year history of hypertension, presented to us with cough for two weeks with intermittent haemoptysis, as well as hoarseness of voice for the past one year. Direct laryngoscopy confirmed that he had left vocal cord palsy. Clinical and radiological investigations suggested that he had left pneumothorax. Left chest tube thoracostomy was performed and computed tomography of chest revealed aortic isthmus aneurysm with dissection extending to distal left common iliac artery and residual left hydropneumothorax. The patient was then referred to the vascular team and cardiothoracic team for further management. John Wiley & Sons, Ltd 2021-02-15 /pmc/articles/PMC7883475/ /pubmed/33614038 http://dx.doi.org/10.1002/rcr2.718 Text en © 2021 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Lo, Shan Min
Ramarmuty, Hema Yamini
Kannan, Kunji
Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title_full Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title_fullStr Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title_full_unstemmed Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title_short Pneumothorax with Ortner syndrome: an unusual presentation of aortic dissection
title_sort pneumothorax with ortner syndrome: an unusual presentation of aortic dissection
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883475/
https://www.ncbi.nlm.nih.gov/pubmed/33614038
http://dx.doi.org/10.1002/rcr2.718
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