Abstract
Tricuspid atresia and aortopulmonary window are rare congenital cardiac anomalies. The occurrence of both these anomalies in the same patient is extremely rare, with only 1 case reported in the literature. We report the surgical management of one such patient and discuss the management issues with respect to Stage 1 single ventricle palliation.
Keywords:
Congenital heart disease; Single ventricle; Tricuspid atresia.
MeSH terms
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Abnormalities, Multiple*
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Aorta / abnormalities
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Aorta / diagnostic imaging
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Aorta / physiopathology
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Aorta / surgery*
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Blood Vessel Prosthesis Implantation
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Cardiac Surgical Procedures* / adverse effects
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Coronary Circulation*
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Echocardiography, Doppler, Color
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Heart Bypass, Right
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Heart Ventricles / abnormalities
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Heart Ventricles / diagnostic imaging
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Heart Ventricles / physiopathology
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Heart Ventricles / surgery*
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Humans
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Infant, Newborn
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Ligation
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Male
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Palliative Care
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Pulmonary Artery / abnormalities
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Pulmonary Artery / diagnostic imaging
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Pulmonary Artery / physiopathology
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Pulmonary Artery / surgery*
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Pulmonary Circulation*
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Reoperation
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Thoracic Duct / surgery
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Thoracotomy
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Treatment Outcome
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Tricuspid Atresia / diagnosis
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Tricuspid Atresia / physiopathology
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Tricuspid Atresia / surgery*