Department of Pediatrics, Pediatric Cardiology, University of Rome La Sapienza, Rome, Italy.
Anat Rec (Hoboken). 2013 Apr;296(4):559-63. doi: 10.1002/ar.22657. Epub 2013 Feb 9.
This study concerns the morphological differentiation between double outlet right ventricle (DORV) and aortic dextroposition (AD) defects, namely tetralogy of Fallot and Eisenmenger anomaly. Indeed, despite the similar condition in terms of sequential ventriculo-arterial connections, DORV and AD are two distinct morphological entities. It is proposed that the borderline between these two groups of malformations is represented by the specific insertion of the infundibular septum into the left anterior cranial division of the septomarginal trabeculation (or septal band) occurring in ADs and lacking in DORV. Furthermore, the spiraliform versus straight parallel arrangement of the great arteries in the two groups of anomalies is emphasized as an additional and distinctive morphological feature. Emphasis is also given to the association of straight parallel great arteries conotruncal malformations, DORV and transposition of the great arteries, with the asplenia type of heterotaxy laterality defects. Within this context, the absence of subaortic ventricular septal defect and concomitantly of spiraliform great arteries in the asplenia group of heterotaxy anomalies, as detected by this study, further substantiates our belief of not mixing collectively the ADs with the DORV in clinico-pathological diagnosis.
本研究关注的是右心室双出口(DORV)和主动脉右位(AD)畸形之间的形态学差异,即法洛四联症和艾森曼格综合征。事实上,尽管在心室-动脉连接的顺序方面相似,但 DORV 和 AD 是两种不同的形态实体。有人提出,这两组畸形之间的界限是由漏斗间隔的特定插入到隔束的左前颅部分(或隔带)来表示的,这种插入仅见于 AD 而不存在于 DORV 中。此外,强调了两组异常中大动脉的螺旋形与直平行排列作为另一个独特的形态特征。还强调了直平行大动脉圆锥干畸形、DORV 和大动脉转位与无脾侧位缺陷的同型异位症的关联。在这种情况下,本研究发现,无脾同型异位症组中不存在主动脉瓣下室间隔缺损和同时存在螺旋形大动脉,进一步证实了我们不在临床病理诊断中集体混合 AD 和 DORV 的信念。