Bohiltea Roxana Elena, Pariza Paul Costin, Stavarache Irina, Munteanu Octavian, Dima Vlad, Mihai Bianca Margareta, Georgescu Tiberiu Augustin, Cinteza Eliza
Department of Obstetrics and Gynecology, "Carol Davila" University of Medicine and Pharmacy Bucharest, Romania.
Department of Radiology, Fundeni Clinical Institute, Bucharest, Romania.
Maedica (Bucur). 2021 Dec;16(4):717-722. doi: 10.26574/maedica.2020.16.4.717.
Double aortic arch represents a congenital vascular malformation that is characterized by the development of a complete vascular ring around the esophagus and trachea due to an anomaly in the development of branchial arteries. We present the case of a 31-year-old gravida that was referred for fetal ultrasound anomalies screening at 22 weeks and six days of gestation. Routine ultrasound scanning of the fetus revealed a structural aortic arch anomaly consistent with a double aortic arch, with no other cardiac and diextracardiac congenital structural malformations. Knowledge of embryology and imaging spectrum of aortic arch anomalies that are able to form vascular rings around the trachea and esophagus are essential for an accurate antenatal diagnosis and therefore, for a correct clinical management.
双主动脉弓是一种先天性血管畸形,其特征是由于鳃动脉发育异常,在食管和气管周围形成一个完整的血管环。我们报告一例31岁孕妇,在妊娠22周零6天时因胎儿超声异常筛查而前来就诊。对胎儿进行的常规超声扫描显示,其主动脉弓结构异常,符合双主动脉弓表现,且无其他心脏及心外先天性结构畸形。了解能够在气管和食管周围形成血管环的主动脉弓畸形的胚胎学及影像学特征,对于准确的产前诊断以及正确的临床处理至关重要。