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Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy
True intrathoracic subclavian artery aneurysms (SCAAs) are rare and have various etiologies. Right intrathoracic SCAAs pose specific anatomic challenges to repair. We present three different operative approaches, open, endovascular, and hybrid repair, for the repair of a right intrathoracic SCAA in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366541/ https://www.ncbi.nlm.nih.gov/pubmed/37496653 http://dx.doi.org/10.1016/j.jvscit.2022.11.018 |
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author | French, Bryce L. Menghini, Anthony M. Burke, Christopher R. Byers, Peter H. Shalhub, Sherene |
author_facet | French, Bryce L. Menghini, Anthony M. Burke, Christopher R. Byers, Peter H. Shalhub, Sherene |
author_sort | French, Bryce L. |
collection | PubMed |
description | True intrathoracic subclavian artery aneurysms (SCAAs) are rare and have various etiologies. Right intrathoracic SCAAs pose specific anatomic challenges to repair. We present three different operative approaches, open, endovascular, and hybrid repair, for the repair of a right intrathoracic SCAA in three patients with genetic arteriopathy: Marfan syndrome, vascular Ehlers-Danlos syndrome, and unspecified Ehlers-Danlos syndrome, respectively. These cases demonstrate an individualized operative approach based on the genetic diagnosis for each patient presenting with a right intrathoracic SCAA. |
format | Online Article Text |
id | pubmed-10366541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103665412023-07-26 Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy French, Bryce L. Menghini, Anthony M. Burke, Christopher R. Byers, Peter H. Shalhub, Sherene J Vasc Surg Cases Innov Tech Case report True intrathoracic subclavian artery aneurysms (SCAAs) are rare and have various etiologies. Right intrathoracic SCAAs pose specific anatomic challenges to repair. We present three different operative approaches, open, endovascular, and hybrid repair, for the repair of a right intrathoracic SCAA in three patients with genetic arteriopathy: Marfan syndrome, vascular Ehlers-Danlos syndrome, and unspecified Ehlers-Danlos syndrome, respectively. These cases demonstrate an individualized operative approach based on the genetic diagnosis for each patient presenting with a right intrathoracic SCAA. Elsevier 2022-12-17 /pmc/articles/PMC10366541/ /pubmed/37496653 http://dx.doi.org/10.1016/j.jvscit.2022.11.018 Text en © 2022 The Author(s) https://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 | Case report French, Bryce L. Menghini, Anthony M. Burke, Christopher R. Byers, Peter H. Shalhub, Sherene Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title | Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title_full | Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title_fullStr | Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title_full_unstemmed | Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title_short | Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
title_sort | operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy |
topic | Case report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366541/ https://www.ncbi.nlm.nih.gov/pubmed/37496653 http://dx.doi.org/10.1016/j.jvscit.2022.11.018 |
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