Abstract

Fetal aortic arch development is an early and complex process that depends on many genetic and environmental factors. The final aortic arch varies greatly; it may take the form of a normal arch, anatomic variant (AAAV) with a common origin to that of the innominate artery and left common carotid artery (formerly known as “bovine aortic arch” (with an incidence of up to 27%)) or one of multiple pathological conditions. The present study aimed to establish the feasibility and impact of prenatal anatomic arch variants’ diagnosis. A retrospective study of 271 fetal second- and third-trimester anomaly scans was performed in our tertiary center. Examinations that evaluated the sagittal aortic arch were included and the branching pattern was assessed. Additionally, a literature data search based on the terms “common origin of innominate artery and left common carotid artery”, “bovine arch”, “bovine aortic” and “aortic arch anomalies” was performed. Results that referred to prenatal AAAV were retained and the papers evaluated. In our study, the AAA incidence was 1.93%, with 4 out of 5 cases being arch type B. All cases had minor associated conditions but a good postnatal outcome. An anatomic aortic variant with a common IA and LCCa prenatal diagnosis was found in a small number of studies; most of the cases described in pediatric and adult series were related to cardiac surgery for stenting, aneurysm or thoracic-associated diseases. The incidence of AAAV varied from 6 to 27% depending on the population studied (highest incidence in African individuals). The variant was highly associated with aortic dissection, pulmonary and cerebral embolism and increased risks of incidents during surgery. Diagnosing AAAV during a routine anatomic scan is feasible and diagnoses can be made when anomaly scans are performed. Awareness of the condition is important for postnatal surgery when other cardiac anomalies are found; this can prevent accidents with simple changes to the patient’s lifestyle, and, in the case of surgery, means we can adopt the correct surgical approach.

Highlights

  • Fetal aortic arch development starts early in pregnancy from the primitive III-d and IV aortic arches and reaches its final circulation pattern at about 57 gestation days, with the process being guided by the neural crest cells [1]

  • The present study aimed to review the significance of the anatomic aortic arch variant with a common origin of the brachiocephalic trunk and left common carotid artery in prenatal examinations

  • An anatomic aortic arch with a common origin of IA and LCCa is a variant of the aortic arch branching with an incidence that can range in adults from 4.8% in Caucasians to 27% in the African population, but the prenatal incidence is not yet clear

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Summary

Introduction

Fetal aortic arch development starts early in pregnancy (around day 41 of gestation) from the primitive III-d and IV aortic arches and reaches its final circulation pattern at about 57 gestation days, with the process being guided by the neural crest cells [1].Many variants of the final aortic arch have been described, some without pathological meaning, i.e., anatomic variants (bovine aortic arch), and others that can affect the fetal and neonatal outcome (double aortic arch, interrupted aortic arch, aortic coarctation) [2].Diagnostics 2022, 12, 624 affect the fetal and neonatal outcome (double aortic arch, interrupted aortic arch, aortic coarctation) [2].Laterality anomalies includes the right aortic arch (RAA) with left arterial ducts or in association with the right arterial duct. Many variants of the final aortic arch have been described, some without pathological meaning, i.e., anatomic variants (bovine aortic arch), and others that can affect the fetal and neonatal outcome (double aortic arch, interrupted aortic arch, aortic coarctation) [2]. Diagnostics 2022, 12, 624 affect the fetal and neonatal outcome (double aortic arch, interrupted aortic arch, aortic coarctation) [2]. Laterality anomalies includes the right aortic arch (RAA) with left arterial ducts or in association with the right arterial duct. As for other cardiac anomalies, the awareness that the anomaly can be detected at the level of 3 vessels view when the arch is coursing to the right of the trachea, increased dramatically the number of detected RAA [3]. Recent systematic review and meta-analysis prove that RAA is associated with an increased risk for congenital heart disease in about 30% of cases, extracardiac defects in 14.1% of cases and mmoorreeoovveerrtotochcrhormomosoosmomalaalbaebrreartriaotnioans 2a2sq2121qd1e1ld(deil G(deiorGgeeosrygnedsryonmder)o(mraen)g(inragnfgroinmg 1fr%omto16%%)tore6g%ar)drleegsasrodflethsseolaf ttehrealliattyeroafltihtyeodfutchtealdaurccthal[4a,r5c]h. [4,5]

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