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Spontaneous aortic rupture in a patient with neurofibromatosis type 1

Neurofibromatosis type I (NF-1) is a rare autosomal dominant genetic disorder occurring in 1 in 3,000 individuals. Vasculopathy is a rarely reported finding in patients with NF-1. Here, we report a case of recurrent aortic pseudoaneurysm after endovascular aneurysm repair in a 49-year-old male patie...

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Autores principales: Park, Yang Jin, Park, Keun Myoung, Oh, Jiyoung, Park, Hong Suk, Kim, Jung-Sun, Kim, Young-Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319782/
https://www.ncbi.nlm.nih.gov/pubmed/22493769
http://dx.doi.org/10.4174/jkss.2012.82.4.261
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author Park, Yang Jin
Park, Keun Myoung
Oh, Jiyoung
Park, Hong Suk
Kim, Jung-Sun
Kim, Young-Wook
author_facet Park, Yang Jin
Park, Keun Myoung
Oh, Jiyoung
Park, Hong Suk
Kim, Jung-Sun
Kim, Young-Wook
author_sort Park, Yang Jin
collection PubMed
description Neurofibromatosis type I (NF-1) is a rare autosomal dominant genetic disorder occurring in 1 in 3,000 individuals. Vasculopathy is a rarely reported finding in patients with NF-1. Here, we report a case of recurrent aortic pseudoaneurysm after endovascular aneurysm repair in a 49-year-old male patient with NF-1. On the sixth postoperative day following a successful open surgical repair of an aortic pseudoaneurysm, he developed hemoperitoneum due to a delayed rupture of the mesenteric artery branch. This was treated with endovascular coil embolization. We report the clinical features and histologic findings of this rare vascular disorder with a review of the relevant literature.
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spelling pubmed-33197822012-04-10 Spontaneous aortic rupture in a patient with neurofibromatosis type 1 Park, Yang Jin Park, Keun Myoung Oh, Jiyoung Park, Hong Suk Kim, Jung-Sun Kim, Young-Wook J Korean Surg Soc Case Report Neurofibromatosis type I (NF-1) is a rare autosomal dominant genetic disorder occurring in 1 in 3,000 individuals. Vasculopathy is a rarely reported finding in patients with NF-1. Here, we report a case of recurrent aortic pseudoaneurysm after endovascular aneurysm repair in a 49-year-old male patient with NF-1. On the sixth postoperative day following a successful open surgical repair of an aortic pseudoaneurysm, he developed hemoperitoneum due to a delayed rupture of the mesenteric artery branch. This was treated with endovascular coil embolization. We report the clinical features and histologic findings of this rare vascular disorder with a review of the relevant literature. The Korean Surgical Society 2012-04 2012-03-27 /pmc/articles/PMC3319782/ /pubmed/22493769 http://dx.doi.org/10.4174/jkss.2012.82.4.261 Text en Copyright © 2012, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/3.0 Journal of the Korean Surgical Society is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Park, Yang Jin
Park, Keun Myoung
Oh, Jiyoung
Park, Hong Suk
Kim, Jung-Sun
Kim, Young-Wook
Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title_full Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title_fullStr Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title_full_unstemmed Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title_short Spontaneous aortic rupture in a patient with neurofibromatosis type 1
title_sort spontaneous aortic rupture in a patient with neurofibromatosis type 1
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319782/
https://www.ncbi.nlm.nih.gov/pubmed/22493769
http://dx.doi.org/10.4174/jkss.2012.82.4.261
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