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1.
Braz J Cardiovasc Surg ; 33(4): 424-427, 2018.
Article in English | MEDLINE | ID: mdl-30184041

ABSTRACT

Aortopulmonary septal defect, also known as the aortopulmonary window, is a rare congenital macrovascular malformation. This case involves a 9-year-old boy with aortopulmonary septal defect (type I combined with type IV). Before surgery, milrinone and alprostadil were used to counteract high lung pressure. Surgery was performed under cardiopulmonary bypass, following which the pulmonary pressure decreased. The aorta was cut, and the right pulmonary artery opening was connected with the main pulmonary artery septal defect using polyester patch. An internal tunnel was made, and the deformity correction was completed. The child exhibited normal postoperative recovery with no discomfort. A complex aortopulmonary window is a rare condition that can be treated successfully with appropriate preoperative and surgical management.


Subject(s)
Aortopulmonary Septal Defect/surgery , Aorta/diagnostic imaging , Aorta/surgery , Aortopulmonary Septal Defect/diagnostic imaging , Aortopulmonary Septal Defect/physiopathology , Blood Pressure , Child , Echocardiography , Humans , Male , Pulmonary Artery/diagnostic imaging , Pulmonary Artery/surgery , Rare Diseases , Tomography, X-Ray Computed , Treatment Outcome
2.
Rev. bras. cir. cardiovasc ; Rev. bras. cir. cardiovasc;33(4): 424-427, July-Aug. 2018. tab, graf
Article in English | LILACS | ID: biblio-958434

ABSTRACT

Abstract Aortopulmonary septal defect, also known as the aortopulmonary window, is a rare congenital macrovascular malformation. This case involves a 9-year-old boy with aortopulmonary septal defect (type I combined with type IV). Before surgery, milrinone and alprostadil were used to counteract high lung pressure. Surgery was performed under cardiopulmonary bypass, following which the pulmonary pressure decreased. The aorta was cut, and the right pulmonary artery opening was connected with the main pulmonary artery septal defect using polyester patch. An internal tunnel was made, and the deformity correction was completed. The child exhibited normal postoperative recovery with no discomfort. A complex aortopulmonary window is a rare condition that can be treated successfully with appropriate preoperative and surgical management.


Subject(s)
Humans , Male , Child , Aortopulmonary Septal Defect/surgery , Aorta/surgery , Aorta/diagnostic imaging , Aortopulmonary Septal Defect/physiopathology , Aortopulmonary Septal Defect/diagnostic imaging , Pulmonary Artery/surgery , Pulmonary Artery/diagnostic imaging , Blood Pressure , Echocardiography , Tomography, X-Ray Computed , Treatment Outcome , Rare Diseases
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