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Hybrid management of a ruptured right subclavian artery aneurysm dissection
Aberrant right subclavian artery is the most common congenital malformation of the aortic arch (0.4%-2.0%). Aneurysms of aberrant subclavian arteries are extremely rare. This results in little experience with their treatment. We describe a case of a patient who presented to the emergency department...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764913/ https://www.ncbi.nlm.nih.gov/pubmed/29349422 http://dx.doi.org/10.1016/j.jvscit.2017.03.003 |
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author | Drullinsky, David Gill, Heather Bayne, Jason P. Morin, Jean-Francois Obrand, Daniel |
author_facet | Drullinsky, David Gill, Heather Bayne, Jason P. Morin, Jean-Francois Obrand, Daniel |
author_sort | Drullinsky, David |
collection | PubMed |
description | Aberrant right subclavian artery is the most common congenital malformation of the aortic arch (0.4%-2.0%). Aneurysms of aberrant subclavian arteries are extremely rare. This results in little experience with their treatment. We describe a case of a patient who presented to the emergency department with a dissection of an aberrant right subclavian artery that later progressed to rupture. Besides hemodynamic instability, this caused an acute superior vena cava syndrome, making airway control difficult. In the operating room, we obtained proximal control through thoracic endovascular aortic repair; median sternotomy was performed for distal control and evacuation of massive hemomediastinum. |
format | Online Article Text |
id | pubmed-5764913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57649132018-01-18 Hybrid management of a ruptured right subclavian artery aneurysm dissection Drullinsky, David Gill, Heather Bayne, Jason P. Morin, Jean-Francois Obrand, Daniel J Vasc Surg Cases Innov Tech Subclavian and internal mammary artery aneurysm Aberrant right subclavian artery is the most common congenital malformation of the aortic arch (0.4%-2.0%). Aneurysms of aberrant subclavian arteries are extremely rare. This results in little experience with their treatment. We describe a case of a patient who presented to the emergency department with a dissection of an aberrant right subclavian artery that later progressed to rupture. Besides hemodynamic instability, this caused an acute superior vena cava syndrome, making airway control difficult. In the operating room, we obtained proximal control through thoracic endovascular aortic repair; median sternotomy was performed for distal control and evacuation of massive hemomediastinum. Elsevier 2017-10-09 /pmc/articles/PMC5764913/ /pubmed/29349422 http://dx.doi.org/10.1016/j.jvscit.2017.03.003 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Subclavian and internal mammary artery aneurysm Drullinsky, David Gill, Heather Bayne, Jason P. Morin, Jean-Francois Obrand, Daniel Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title | Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title_full | Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title_fullStr | Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title_full_unstemmed | Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title_short | Hybrid management of a ruptured right subclavian artery aneurysm dissection |
title_sort | hybrid management of a ruptured right subclavian artery aneurysm dissection |
topic | Subclavian and internal mammary artery aneurysm |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764913/ https://www.ncbi.nlm.nih.gov/pubmed/29349422 http://dx.doi.org/10.1016/j.jvscit.2017.03.003 |
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