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Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries

We report a case of 55 mm abdominal aortic aneurysm coinciding with a rare congenital anomaly of proximal origin of bilateral internal iliac arteries (IIAs). Because renal to iliac bifurcation lengths were bilaterally short (129 mm and 125 mm), a trunk-ipsilateral leg and an iliac leg were deployed...

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Detalles Bibliográficos
Autores principales: Shirasu, Takuro, Akai, Atsushi, Motoki, Manabu, Kato, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033981/
https://www.ncbi.nlm.nih.gov/pubmed/36970131
http://dx.doi.org/10.1016/j.jvscit.2023.101119
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author Shirasu, Takuro
Akai, Atsushi
Motoki, Manabu
Kato, Masaaki
author_facet Shirasu, Takuro
Akai, Atsushi
Motoki, Manabu
Kato, Masaaki
author_sort Shirasu, Takuro
collection PubMed
description We report a case of 55 mm abdominal aortic aneurysm coinciding with a rare congenital anomaly of proximal origin of bilateral internal iliac arteries (IIAs). Because renal to iliac bifurcation lengths were bilaterally short (129 mm and 125 mm), a trunk-ipsilateral leg and an iliac leg were deployed before iliac branch component insertion into the iliac leg. With help of a pull-through wire, internal iliac component was delivered without migration of the main body. The left IIA was embolized, but the right IIA was successfully preserved with commercially available iliac branch endoprosthesis only from femoral approaches, and the patient fully recovered without any complication.
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spelling pubmed-100339812023-03-24 Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries Shirasu, Takuro Akai, Atsushi Motoki, Manabu Kato, Masaaki J Vasc Surg Cases Innov Tech Case report We report a case of 55 mm abdominal aortic aneurysm coinciding with a rare congenital anomaly of proximal origin of bilateral internal iliac arteries (IIAs). Because renal to iliac bifurcation lengths were bilaterally short (129 mm and 125 mm), a trunk-ipsilateral leg and an iliac leg were deployed before iliac branch component insertion into the iliac leg. With help of a pull-through wire, internal iliac component was delivered without migration of the main body. The left IIA was embolized, but the right IIA was successfully preserved with commercially available iliac branch endoprosthesis only from femoral approaches, and the patient fully recovered without any complication. Elsevier 2023-02-10 /pmc/articles/PMC10033981/ /pubmed/36970131 http://dx.doi.org/10.1016/j.jvscit.2023.101119 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
Shirasu, Takuro
Akai, Atsushi
Motoki, Manabu
Kato, Masaaki
Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title_full Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title_fullStr Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title_full_unstemmed Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title_short Modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
title_sort modified adaption of iliac branch endografts in rare congenital anomaly of proximal origin of bilateral internal iliac arteries
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033981/
https://www.ncbi.nlm.nih.gov/pubmed/36970131
http://dx.doi.org/10.1016/j.jvscit.2023.101119
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