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Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass
Profunda femoris artery aneurysms (PFAAs) are rare and account for only 0.5% of all peripheral artery aneurysms. Potential complications include compression of surrounding nerves and veins, limb ischemia, and rupture. Currently there are no guidelines on the management of true PFAAs, and suggested t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033977/ https://www.ncbi.nlm.nih.gov/pubmed/36970133 http://dx.doi.org/10.1016/j.jvscit.2023.101097 |
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author | Kattih, Obada Harry, Lauren Baldwin, Erin |
author_facet | Kattih, Obada Harry, Lauren Baldwin, Erin |
author_sort | Kattih, Obada |
collection | PubMed |
description | Profunda femoris artery aneurysms (PFAAs) are rare and account for only 0.5% of all peripheral artery aneurysms. Potential complications include compression of surrounding nerves and veins, limb ischemia, and rupture. Currently there are no guidelines on the management of true PFAAs, and suggested treatment modalities include endovascular, open, and hybrid approaches. We report a case of an 82-year-old male with a history of aneurysmal disease who presented with a symptomatic 6.5-cm PFAA. He underwent successful aneurysmectomy and interposition bypass, which remains an effective method for treatment of this rare pathology. |
format | Online Article Text |
id | pubmed-10033977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100339772023-03-24 Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass Kattih, Obada Harry, Lauren Baldwin, Erin J Vasc Surg Cases Innov Tech Case report Profunda femoris artery aneurysms (PFAAs) are rare and account for only 0.5% of all peripheral artery aneurysms. Potential complications include compression of surrounding nerves and veins, limb ischemia, and rupture. Currently there are no guidelines on the management of true PFAAs, and suggested treatment modalities include endovascular, open, and hybrid approaches. We report a case of an 82-year-old male with a history of aneurysmal disease who presented with a symptomatic 6.5-cm PFAA. He underwent successful aneurysmectomy and interposition bypass, which remains an effective method for treatment of this rare pathology. Elsevier 2023-01-13 /pmc/articles/PMC10033977/ /pubmed/36970133 http://dx.doi.org/10.1016/j.jvscit.2023.101097 Text en © 2023 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 Kattih, Obada Harry, Lauren Baldwin, Erin Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title | Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title_full | Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title_fullStr | Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title_full_unstemmed | Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title_short | Successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
title_sort | successful treatment of a rare 6.5-cm true profunda femoris artery aneurysm with aneurysmectomy and interposition bypass |
topic | Case report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033977/ https://www.ncbi.nlm.nih.gov/pubmed/36970133 http://dx.doi.org/10.1016/j.jvscit.2023.101097 |
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