This is a heart with double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis.
This is a congenital cardiovascular malformation that is a variant of double outlet right ventricle with concordant atrioventricular connections, a doubly committed ventricular septal defect with absence or deficiency of the conal septum, and pulmonary outflow tract obstruction.
The aorta and pulmonary trunk both arise from the morphologic right ventricle. The aorta is anterior to the pulmonary trunk. There is narrowing of the pulmonary trunk. There is a systemic to pulmonary artery shunt that arises from the ascending aorta to the pulmonary arteries.
There is an interventricular communication that is an outlet type of defect as it lives within the “Y” of the septal band. Phrased alternatively it lies within the cranial and caudal limbs of the septomarginal trabeculation.
IPCCC classification (01.01.17 + 07.13.02).
Scanned with Revopoint mini 2.
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