Your browser doesn't support javascript.
loading
Aortic arch advancement for type A interrupted aortic arch with persistent fifth aortic arch type B.
Binsalamah, Ziyad M; Chen, Peter; McKenzie, Emmett D.
Afiliación
  • Binsalamah ZM; Michael E. DeBakey Department of Surgery,Division of Congenital Heart Surgery,Baylor College of Medicine,Houston,Texas,United States of America.
  • Chen P; Michael E. DeBakey Department of Surgery,Division of Congenital Heart Surgery,Baylor College of Medicine,Houston,Texas,United States of America.
  • McKenzie ED; Michael E. DeBakey Department of Surgery,Division of Congenital Heart Surgery,Baylor College of Medicine,Houston,Texas,United States of America.
Cardiol Young ; 27(5): 1018-1021, 2017 Jul.
Article en En | MEDLINE | ID: mdl-28260541
ABSTRACT
Persistence of the fifth aortic arch is a very rare anomaly, but is clinically relevant when it is associated with coarctation. We report a case of a neonate with type A interrupted aortic arch and severe coarctation of a persistent fifth aortic arch, which was discovered after repair of a left congenital diaphragmatic hernia. The combination of anomalies was discovered intra-operatively following left thoracotomy, and was treated with aortic arch advancement. The postoperative course was uneventful.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Coartación Aórtica / Hernias Diafragmáticas Congénitas Límite: Female / Humans / Newborn Idioma: En Revista: Cardiol Young Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Coartación Aórtica / Hernias Diafragmáticas Congénitas Límite: Female / Humans / Newborn Idioma: En Revista: Cardiol Young Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos
...