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Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome

Loeys-Dietz syndrome is a rare connective tissue disorder with widespread arterial tortuosity and aneurysms. This syndrome is most notable for its aortic disease, including aortic root dilation and aortic dissection or rupture. Although not as well studied, peripheral artery aneurysms are a prevalen...

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Detalles Bibliográficos
Autores principales: Wang, Sophie, Kernodle, Amber, Hicks, Caitlin W., Black, James Hamilton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013001/
https://www.ncbi.nlm.nih.gov/pubmed/29942909
http://dx.doi.org/10.1016/j.jvscit.2018.03.001
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author Wang, Sophie
Kernodle, Amber
Hicks, Caitlin W.
Black, James Hamilton
author_facet Wang, Sophie
Kernodle, Amber
Hicks, Caitlin W.
Black, James Hamilton
author_sort Wang, Sophie
collection PubMed
description Loeys-Dietz syndrome is a rare connective tissue disorder with widespread arterial tortuosity and aneurysms. This syndrome is most notable for its aortic disease, including aortic root dilation and aortic dissection or rupture. Although not as well studied, peripheral artery aneurysms are a prevalent concurrent manifestation and have previously been repaired with both open and endovascular approaches. There are minimal data about the durability and technical considerations of endovascular repair in this disease. We report a case of a patient who developed an extremely tortuous recurrent femoral-popliteal artery aneurysm secondary to aneurysmal degeneration around previously placed stents that was treated with an endovascular approach.
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spelling pubmed-60130012018-06-25 Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome Wang, Sophie Kernodle, Amber Hicks, Caitlin W. Black, James Hamilton J Vasc Surg Cases Innov Tech Case report Loeys-Dietz syndrome is a rare connective tissue disorder with widespread arterial tortuosity and aneurysms. This syndrome is most notable for its aortic disease, including aortic root dilation and aortic dissection or rupture. Although not as well studied, peripheral artery aneurysms are a prevalent concurrent manifestation and have previously been repaired with both open and endovascular approaches. There are minimal data about the durability and technical considerations of endovascular repair in this disease. We report a case of a patient who developed an extremely tortuous recurrent femoral-popliteal artery aneurysm secondary to aneurysmal degeneration around previously placed stents that was treated with an endovascular approach. Elsevier 2018-04-30 /pmc/articles/PMC6013001/ /pubmed/29942909 http://dx.doi.org/10.1016/j.jvscit.2018.03.001 Text en © 2018 The Author(s) 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 Case report
Wang, Sophie
Kernodle, Amber
Hicks, Caitlin W.
Black, James Hamilton
Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title_full Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title_fullStr Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title_full_unstemmed Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title_short Endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with Loeys-Dietz syndrome
title_sort endovascular repair of tortuous recurrent femoral-popliteal aneurysm in a patient with loeys-dietz syndrome
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013001/
https://www.ncbi.nlm.nih.gov/pubmed/29942909
http://dx.doi.org/10.1016/j.jvscit.2018.03.001
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