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Right pulmonary artery originating from the ascending aorta with tetralogy of fallot and pulmonary atresia.
Rorris, Filippos-Paschalis; Kanakis, Meletios; Samanidis, George; Tsoutsinos, Alexandros; Lioulias, Achilleas; Bobos, Dimitrios.
Afiliación
  • Rorris FP; Department of Paediatric and Adult Congenital Heart Surgery Onassis Cardiac Center Athens Greece.
  • Kanakis M; Department of Paediatric and Adult Congenital Heart Surgery Onassis Cardiac Center Athens Greece.
  • Samanidis G; 1st Department of Adult Cardiac Surgery Onassis Cardiac Surgery Center Athens Greece.
  • Tsoutsinos A; Department of Paediatric Cardiology and Adult Congenital Heart Disease Onassis Cardiac Surgery Centre Athens Greece.
  • Lioulias A; Department of Paediatric and Adult Congenital Heart Surgery Onassis Cardiac Center Athens Greece.
  • Bobos D; Department of Paediatric and Adult Congenital Heart Surgery Onassis Cardiac Center Athens Greece.
Clin Case Rep ; 12(8): e9232, 2024 Aug.
Article en En | MEDLINE | ID: mdl-39139621
ABSTRACT
Key Clinical Message Anomalous origin of right pulmonary artery from the ascending aorta is a rare congenital heart malformation that results in early infant mortality. These patients are at risk for the early development of significant pulmonary hypertension. The surgical management during the early period of life is imperative. Abstract Anomalous pulmonary artery originating from the ascending aorta (often called hemitruncus) is a rare congenital cardiac defect requiring immediate management in the neonatal period. We report a case of a rare variant of anomalous right pulmonary artery originating from the ascending aorta in combination with pulmonary atresia and tetralogy of Fallot. The above-mentioned combination makes the surgical management of such cardiac defect exceedingly demanding.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2024 Tipo del documento: Article