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Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome

Marfan syndrome is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1). This leads to defective elasticity of connective tissue in the arterial wall. Aortic aneurysms and dissections are the most common vascular anomalies; the incidence of peripheral artery aneurysms is...

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Autores principales: Peng, Kate Xin, Davila, Victor J., Fowl, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806640/
https://www.ncbi.nlm.nih.gov/pubmed/31660457
http://dx.doi.org/10.1016/j.jvscit.2018.08.008
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author Peng, Kate Xin
Davila, Victor J.
Fowl, Richard J.
author_facet Peng, Kate Xin
Davila, Victor J.
Fowl, Richard J.
author_sort Peng, Kate Xin
collection PubMed
description Marfan syndrome is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1). This leads to defective elasticity of connective tissue in the arterial wall. Aortic aneurysms and dissections are the most common vascular anomalies; the incidence of peripheral artery aneurysms is not well understood. Treatment options for infrainguinal disease are limited as endovascular interventions are generally contraindicated. The best conduit for arterial reconstruction is also unknown because there is concern that saphenous vein may become aneurysmal. Currently, there are few case reports regarding outcomes of infrainguinal arterial reconstructions, and follow-up has been very short term. We report a rare case of successful repair of a popliteal aneurysm using a saphenous vein graft in a patient with Marfan syndrome.
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spelling pubmed-68066402019-10-28 Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome Peng, Kate Xin Davila, Victor J. Fowl, Richard J. J Vasc Surg Cases Innov Tech Popliteal aneurysm Marfan syndrome is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1). This leads to defective elasticity of connective tissue in the arterial wall. Aortic aneurysms and dissections are the most common vascular anomalies; the incidence of peripheral artery aneurysms is not well understood. Treatment options for infrainguinal disease are limited as endovascular interventions are generally contraindicated. The best conduit for arterial reconstruction is also unknown because there is concern that saphenous vein may become aneurysmal. Currently, there are few case reports regarding outcomes of infrainguinal arterial reconstructions, and follow-up has been very short term. We report a rare case of successful repair of a popliteal aneurysm using a saphenous vein graft in a patient with Marfan syndrome. Elsevier 2019-09-17 /pmc/articles/PMC6806640/ /pubmed/31660457 http://dx.doi.org/10.1016/j.jvscit.2018.08.008 Text en © 2018 Published by Elsevier Inc. on behalf of Society for Vascular Surgery. 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 Popliteal aneurysm
Peng, Kate Xin
Davila, Victor J.
Fowl, Richard J.
Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title_full Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title_fullStr Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title_full_unstemmed Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title_short Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
title_sort successful repair of a popliteal aneurysm with saphenous vein graft in a patient with marfan syndrome
topic Popliteal aneurysm
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806640/
https://www.ncbi.nlm.nih.gov/pubmed/31660457
http://dx.doi.org/10.1016/j.jvscit.2018.08.008
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