| Literature DB >> 33680709 |
Annie Le-Nguyen1, Shahrzad Joharifard2, Geneviève Côté3, Daniel Borsuk4, Rafik Ghali5, Michel Lallier2.
Abstract
Congenital abdominal aortic aneurysms (AAA) are an extremely rare entity. We present the case of a female fetus diagnosed with an AAA on routine prenatal ultrasound. A postnatal computed tomography angiogram revealed an infrarenal AAA with a narrow proximal neck. Surgery was performed on day of life 14 using a cadaveric femoral artery graft. The proximal anastomosis was performed under the microscope given the severity of the aortic stenosis and the proximity of the renal arteries. The patient's postoperative course was uneventful and she is developing normally 1 year after surgery. The graft remains permeable, albeit with evidence of proximal and distal stenosis and graft calcification on imaging. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ).Entities:
Keywords: abdominal; aortic aneurysm; congenital; neonatal; surgical repair
Year: 2021 PMID: 33680709 PMCID: PMC7929720 DOI: 10.1055/s-0041-1723019
Source DB: PubMed Journal: European J Pediatr Surg Rep ISSN: 2194-7619