A new anatomic approach of the ventricular septal defect in the interruption of the aortic arch. Issue 2 (7th December 2018)

• Record Type: Journal Article
• Authors: Mostefa Kara, Meriem; Houyel, Lucile; Bonnet, Damien
• Is Part Of: Journal of anatomy. Volume 234:Issue 2(2019)
• Page Start: 193
• Page End: 200
• Publication Date: 2018-12-07
• Subjects: congenital heart disaese -- interruption aortic arch -- ventricular septal defect; Anatomy -- Periodicals; 571.3
• DOI: 10.1111/joa.12911
• Languages: English
• ISSNs: 0021-8782

Abstract

Abstract: The aim of this study was to analyse the anatomy of the ventricular septal defect (VSD) in heart specimens with interruption of the aortic arch (IAA) in order to explore the hypothesis of different embryologic mechanisms for the different anatomic types of IAA. We examined 42 human heart specimens, 25 with IAA as the main disease with concordant atrioventricular and ventriculo‐arterial connections and two distinct great arteries, and 17 hearts with IAA associated with other malformations [six common arterial trunk (CAT), five double‐outlet right ventricle (DORV), three transposition of the great arteries (TGA), three atrioventricular septal defect (AVSD)]. The interruption was classified according to Celoria and Patton. We focused on the anatomy of the VSD viewed from the right ventricular side. There were 15 IAA type A, 27 type B, no type C. The VSD in IAA type B was always an outlet VSD, located between the two limbs of the septal band, with posterior malalignment of the outlet septum in hearts with concordant ventriculo‐arterial connections, without any fibrous tricuspid‐aortic continuity. In addition, the aortic arch was always completely absent. Conversely, the VSD in IAA type A could be of any type (outlet in six, muscular in four, central perimembranous in two, inlet in three) and the aortic arch was either atretic or absent. In addition, IAA type B, when found in the setting of another anomaly, was always associated with neural crest‐related anomalies (CAT and DORV), whereas IAA type A was found in association with anomalies not related to the neural crest (TGA and AVSD). These results reinforce the hypothesis that different pathogenic mechanisms are responsible for the two types of IAA, and the inclusion of IAA type B in the group of neural crest defects. Conversely, IAA type A could be due to overlapping mechanisms: flow‐related defect (coarctation‐like) and neural crest contribution.