No abstract available.
Aorta* ; Aortopulmonary Septal Defect ; Pulmonary Artery*

No abstract available.
Aorta, Thoracic* ; Aortopulmonary Septal Defect* ; Pulmonary Artery*

Humans ; Aortopulmonary Septal Defect/surgery* ; Septal Occluder Device

Humans ; Aortopulmonary Septal Defect/surgery* ; Septal Occluder Device

Aortopulmonary Septal Defect ; therapy ; Catheterization ; Female ; Humans ; Infant

Aortopulmonary window (APW) is a rare cardiac anomaly that was reported to occur in only 43 cases over 33 years at a large-volume cardiac center. It can present as an isolated anomaly or in combination with another cardiac anomaly. The surgical technique for APW has evolved from simple ligation to separation of the 2 great arteries. However, because of the rarity of APW, there is no standard surgical treatment for this disease entity. Herein, we present successful aortic reconstruction using a main pulmonary artery flap after separation of the 2 great arteries in a neonate with isolated APW.
Aortopulmonary Septal Defect ; Arteries ; Humans ; Infant, Newborn ; Ligation ; Pulmonary Artery

Interrupted aortic arch with an aortopulmonary window is a rare congenital entity that is associated with high morbidity and mortality, especially in premature low-birth-weight infants, and the proper timing of surgical correction remains a matter of debate. We present the case of a premature infant weighing 1.6 kg who successfully underwent one stage surgical repair to treat interrupted aortic arch with an aortopulmonary window. The therapeutic management of this patient is described below, and a review of the literature is presented.
Aorta, Thoracic* ; Aortopulmonary Septal Defect ; Humans ; Infant, Low Birth Weight ; Infant, Newborn* ; Infant, Premature ; Mortality

Aortopulmonary Septal Defect ; diagnostic imaging ; surgery ; Female ; Humans ; Infant ; Tomography, X-Ray Computed ; methods

Adult ; Aortopulmonary Septal Defect ; diagnosis ; pathology ; Echocardiography ; methods ; Female ; Heart Septal Defects, Ventricular ; diagnosis ; pathology ; Humans ; Pregnancy ; Prenatal Diagnosis ; methods

Aortopulmonary septal defect is a rare congenital cardiac anomaly. A 15 year old boy was admitted to Department of Internal Medicine of Seoul National University Hospital because of exertional dyspnea. Aortopulmonary septal defect was confirmed by cardiac catheterization demonstrating severe pulmonary hypertension and patent foramen ovale, and retrograde aortogram showing contrast material passing from the ascending aorta just above the aortic valve into the pulmonary trunk. We present a case of aortopulmonary septal defect with a review of literatures.
Adolescent ; Aorta ; Aortic Valve ; Aortopulmonary Septal Defect* ; Cardiac Catheterization ; Cardiac Catheters ; Dyspnea ; Foramen Ovale, Patent ; Humans ; Hypertension, Pulmonary ; Internal Medicine ; Male ; Seoul