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Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia
Aneurysms of the intra-thoracic subclavian artery (SCA) are rare. They are often revealed by complications. Surgical treatment is always indicated. Endovascular treatment is a less invasive alternative. We report a case of a 60 years-old woman admitted for right chest pain and dysphonia. Laryngoscop...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215561/ https://www.ncbi.nlm.nih.gov/pubmed/22355438 |
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author | Mechchat, Alae El Hammoumi, Massine M EL Mesnaoui, Abbas Lekehal, Brahim Bensaid, Youness |
author_facet | Mechchat, Alae El Hammoumi, Massine M EL Mesnaoui, Abbas Lekehal, Brahim Bensaid, Youness |
author_sort | Mechchat, Alae |
collection | PubMed |
description | Aneurysms of the intra-thoracic subclavian artery (SCA) are rare. They are often revealed by complications. Surgical treatment is always indicated. Endovascular treatment is a less invasive alternative. We report a case of a 60 years-old woman admitted for right chest pain and dysphonia. Laryngoscopy noted a right vocal cord palsy. Chest computed tomography and angiography showed a giant aneurysm of the intra-thoracic right SCA. A resection-ligation of the aneurysm was performed by a supra-clavicular approach. Postoperative course was uneventful. The histology defined an atherosclerotic aneurysm. The patient underwent voice reeducation with partial improvement after six months. |
format | Online Article Text |
id | pubmed-3215561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-32155612012-02-21 Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia Mechchat, Alae El Hammoumi, Massine M EL Mesnaoui, Abbas Lekehal, Brahim Bensaid, Youness Pan Afr Med J Case Report Aneurysms of the intra-thoracic subclavian artery (SCA) are rare. They are often revealed by complications. Surgical treatment is always indicated. Endovascular treatment is a less invasive alternative. We report a case of a 60 years-old woman admitted for right chest pain and dysphonia. Laryngoscopy noted a right vocal cord palsy. Chest computed tomography and angiography showed a giant aneurysm of the intra-thoracic right SCA. A resection-ligation of the aneurysm was performed by a supra-clavicular approach. Postoperative course was uneventful. The histology defined an atherosclerotic aneurysm. The patient underwent voice reeducation with partial improvement after six months. The African Field Epidemiology Network 2011-08-17 /pmc/articles/PMC3215561/ /pubmed/22355438 Text en © Alae Mechchat et al. http://creativecommons.org/licenses/by/2.0 The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of 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 Mechchat, Alae El Hammoumi, Massine M EL Mesnaoui, Abbas Lekehal, Brahim Bensaid, Youness Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title | Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title_full | Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title_fullStr | Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title_full_unstemmed | Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title_short | Giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
title_sort | giant aneurysm of the right intra thoracic sub-clavian artery presenting as a dysphonia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215561/ https://www.ncbi.nlm.nih.gov/pubmed/22355438 |
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