Mi Kyoung Song¹, Gi Beom Kim¹, Woong Han Kim², Whal Lee³, Eun-Jung Bae^1,*

Congenital Heart Disease, Vol.17, No.4, pp. 393-398, 2022, DOI:10.32604/chd.2022.019603 - 04 July 2022

Abstract We report the case of a rare complex cardiac anomaly involving situs solitus, concordant atrioventricular connection with left-hand ventricular topology, and L-looped ventricles. The ventricles had a superior-inferior relationship with an inferiorly located right ventricle, which had a double outlet with far posteriorly located great arteries. The left atrium was elongated, with juxta-positioned atrial appendages on the right side. The 3D-printed model using a computed tomography scan taken on the fourth day of birth demonstrated the anatomy clearly and helped us decide on the surgical management. More > Graphic Abstract

Gregory Perens^1,*, Takegawa Yoshida², J. Paul Finn²

Congenital Heart Disease, Vol.17, No.4, pp. 387-392, 2022, DOI:10.32604/chd.2022.021233 - 04 July 2022

Abstract An infant male presented with the rare anatomy consisting of situs solitus, concordant atrioventricular connections to L-looped ventricles, double outlet right ventricle (DORV), and hypoplastic aortic arch. 6 months after neonatal aortic arch repair, the morphologic right ventricle function deteriorated, and surgical evaluation was undertaken to determine if either biventricular repair with a systemic morphologic left ventricle or right ventricular exclusion was possible. After initial echocardiography, magnetic resonance imaging (MRI) was used to create detailed axial and 4-dimensional (4D) images and 3-dimensional (3D) printed models. The detailed anatomy of this rare, complex case and its More > Graphic Abstract