Literature DB >> 24981107

Surgical management of a hypoplastic distal aortic arch and coarctation of aorta in a patient with Klippel-Feil syndrome, ascending aortic aneurysm and bicuspid aortic valve.

Frantisek Sabol1, Adrián Kolesar2, Tomás Toporcer1, Milan Bajmoczi3.   

Abstract

Klippel-Feil syndrome has been associated with cardiovascular malformations, but only 3 cases have been reported to be associated with aortic coarctation and surgical management is not defined. A 51-year old woman with Klippel-Feil syndrome associated with an aneurysm of the ascending aorta, hypoplastic aortic arch and aortic coarctation at the level of the left subclavian artery presented with shortness of breath 2 years after diagnosis. Imaging identified interim development of a 7.2-cm aneurysm at the level of the aortic coarctation. She underwent surgical repair with a Dacron interposition graft under hypothermic circulatory arrest. She continues to do well 18 months following repair.
© The Author 2014. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Entities:  

Keywords:  Aortic coarctation; Hypoplastic distal arch; Klippel–Feil syndrome

Mesh:

Substances:

Year:  2014        PMID: 24981107     DOI: 10.1093/icvts/ivu193

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  1 in total

1.  Aortic stenosis of a bicuspid aortic valve in a patient with Klippel-Feil syndrome: a case report.

Authors:  Rory F L Hammond; Sara Jasionowska; Wael I Awad
Journal:  Eur Heart J Case Rep       Date:  2020-03-24
  1 in total

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