Chatila Sami, Houyel Lucile, Hily Manon, Bonnet Damien
Congenital and Pediatric Cardiology Unit, M3C-Necker, Hôpital Necker-Enfants Malades, AP-HP, 75015 Paris, France.
Université de Paris, 75006 Paris, France.
J Cardiovasc Dev Dis. 2021 Dec 6;8(12):175. doi: 10.3390/jcdd8120175.
Common arterial trunk (CAT) is a rare congenital heart disease that is commonly included into the spectrum of conotruncal heart defects. CAT is rarely associated with functionally univentricular hearts, and only few cases have been described so far. Here, we describe the anatomical characteristics of CAT associated with a univentricular heart diagnosed in children and fetuses referred to our institution, and we completed the anatomical description of this rare condition through an extensive review of the literature. The complete cohort ultimately gathered 32 cases described in the literature completed by seven cases from our unit (seven fetuses and one child). Four types of univentricular hearts associated with CAT were observed: tricuspid atresia or hypoplastic right ventricle in 16 cases, mitral atresia or hypoplastic left ventricle in 12 cases, double-inlet left ventricle in 2 cases, and unbalanced atrioventricular septal defect in 9 cases. Our study questions the diagnosis of CAT as the exclusive consequence of an anomaly of the wedging process, following the convergence between the embryonic atrioventricular canal and the common outflow tract. We confirm that some forms of CAT can be considered to be due to an arrest of cardiac development at the stages preceding the convergence.
共同动脉干(CAT)是一种罕见的先天性心脏病,通常被纳入圆锥动脉干心脏缺陷的范畴。CAT很少与功能性单心室心脏相关,迄今为止仅有少数病例被描述。在此,我们描述了转诊至我们机构的儿童和胎儿中诊断出的与单心室心脏相关的CAT的解剖学特征,并通过广泛的文献回顾完成了对这种罕见病症的解剖学描述。完整的队列最终收集了文献中描述的32例病例,并补充了我们科室的7例病例(7例胎儿和1例儿童)。观察到与CAT相关的四种类型的单心室心脏:三尖瓣闭锁或右心室发育不全16例,二尖瓣闭锁或左心室发育不全12例,双入口左心室2例,不平衡房室间隔缺损9例。我们的研究对将CAT诊断为胚胎房室管与共同流出道汇合后楔入过程异常的唯一后果提出了质疑。我们证实,某些形式的CAT可被认为是由于在汇合前阶段心脏发育停滞所致。