Hostname: page-component-77c89778f8-swr86 Total loading time: 0 Render date: 2024-07-16T12:07:27.307Z Has data issue: false hasContentIssue false
  • English
  • Français

Prenatal diagnosis and perinatal clinical course of isolated left-sided innominate artery

Published online by Cambridge University Press:  27 May 2024

Shinichiro Sakaki Open the ORCID record for Shinichiro Sakaki [Opens in a new window] ,
Takeshi Ikegawa ,
Motoyoshi Kawataki  and
Hideaki Ueda
Shinichiro Sakaki*
Affiliation:
Department of Cardiology, Kanagawa Children’s Medical Center, Kanagawa, Japan
Takeshi Ikegawa
Affiliation:
Department of Cardiology, Kanagawa Children’s Medical Center, Kanagawa, Japan
Motoyoshi Kawataki
Affiliation:
Department of Neonatology, Kanagawa Children’s Medical Center, Kanagawa, Japan
Hideaki Ueda
Affiliation:
Department of Cardiology, Kanagawa Children’s Medical Center, Kanagawa, Japan
*
Corresponding author: S. Sakaki; Email: sakaki413@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Isolated left-sided innominate artery, a rare congenital anomaly in which the left-sided innominate artery arises from the main pulmonary trunk, is usually diagnosed incidentally in children and adults. Limited reports exist on its prenatal diagnosis, with none comprehensively describing the associated perinatal haemodynamic changes. We report a case of prenatally diagnosed isolated left-sided innominate artery, describing the postnatal clinical course.

Keywords

fetal cardiac echoCHDaortic arch anomaly
Type
Brief Report
Information
Cardiology in the Young , First View , pp. 1 - 3
Check for updates
Copyright
© The Author(s), 2024. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Crawford, T. An atlas of vascular rings and related malformations of the aortic arch system. J Clin Pathol 1964; 17: 579–580.CrossRefGoogle Scholar
Fong, LV, Venables, AW. Isolation of the left common carotid or left innominate artery. Br Heart J 1987; 57: 552–554.CrossRefGoogle ScholarPubMed
Li, Y, Zhang, X, Yan, Y, Pei, Q. Prenatal ultrasonic diagnosis and prognostic analysis of isolated left subclavian artery (ILSCA) and left brachiocephalic trunk (ILBCT) malformation. Pediatr Cardiol 2018; 39: 1650–1655.CrossRefGoogle ScholarPubMed
Hao, XY, Zhang, Y, Zhao, Y, et al. Prenatal diagnosis of isolation of aortic brachiocephalic artery. Acta Radiol 2022; 63: 1712–1720.CrossRefGoogle ScholarPubMed
Park, MK. Right aortic arch with isolation of left innominate artery. Chest 1979; 76: 106–108.CrossRefGoogle ScholarPubMed
Gowda, SLG, Bhat, PS, Jayaranganath, M, Hegde, M. Isolated left brachiocephalic trunk arising from the main pulmonary artery with right aortic arch. J Thorac Cardiovasc Surg 2014; 147: 822–823.CrossRefGoogle Scholar
Reeves, BM, Colen, TM, Sheridan, BJ, Ward, C. Isolated innominate artery as a cause of subclavian steal and cerebral hemisphere atrophy. Pediatr Cardiol 2010; 31: 1083–1085.CrossRefGoogle ScholarPubMed
Le Bret, E, Leobon, B, Roubertie, F, et al. Right aortic arch and isolated left innominate artery from a left sided patent ductus arteriosus: a very rare aortic arch anomaly. J Pediatr Surg 2009; 44: E29–E31.CrossRefGoogle ScholarPubMed
Maier, HC, Van der Woude, R. Right-sided patent ductus arteriosus with right aortic arch. J Thorac Cardiovasc Surg 1968; 56: 401–407.CrossRefGoogle ScholarPubMed