Isolated aberrant right subclavian artery. A case report

• Autores: Monzón Castillo, Eli Pedro, Tejada Martínez, Gabriel
• Formato: artículo
• Fecha de Publicación: 2020
• Institución: Sociedad Peruana de Obstetricia y Ginecología
• Repositorio: Revista SPOG - Revista Peruana de Ginecología y Obstetricia
• Lenguaje: español; inglés
• OAI Identifier: oai:ojs.spog:article/2266
• Enlace del recurso: http://www.spog.org.pe/web/revista/index.php/RPGO/article/view/2266
• Nivel de acceso: acceso abierto
• Materia: Aberrant right subclavian artery (ARSA); Down syndrome; Arteria subclavia derecha aberrante (ARSA); Síndrome de Down

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.