Isolated aberrant right subclavian artery. A case report

Authors

  • Eli Pedro Monzón Castillo Adjunct Gynecologyst; Gynecology and Obstetrics Service, Hospital de Hellín, Albacete, España
  • Gabriel Tejada Martínez Head of Service; Gynecology and Obstetrics Service, Hospital de Hellín, Albacete, España

DOI:

https://doi.org/10.31403/rpgo.v66i2266

Keywords:

Aberrant right subclavian artery (ARSA), Down syndrome

Abstract

An aberrant right subclavian artery (ARSA) is the most common branching abnormality of the aortic arch. It can be identified by ultrasound scan in 1% of the cases. The probability of association with cardiac and/or extracardiac anomalies, as well as chromosomal abnormality, is high. The prevalence of ARSA with Down syndrome is approximately 20%, and this marker may contribute to counseling in Down syndrome during the second trimester and maybe in the first trimester. Recommendations when finding an ARSA is to carry out a detailed study of the fetal anatomy looking for other markers of the aneuploidy and to perform a fetal echocardiogram. The performance of invasive studies will be limited to those situations where, in addition to the ARSA, other markers or other conditions that increase the risk of Down syndrome are found. However, the finding of an isolated ARSA increases the risk to zero, and is considered a normal variant.

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Published

2020-11-06

How to Cite

Monzón Castillo, E. P., & Tejada Martínez, G. (2020). Isolated aberrant right subclavian artery. A case report. The Peruvian Journal of Gynecology and Obstetrics, 66(3). https://doi.org/10.31403/rpgo.v66i2266

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Section

Casos Clínicos

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