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Incomplete isolation of the left innominate artery from the right aortic arch: a rare case of double-outlet right ventricle with pulmonary stenosis

Part of: Cardiac Morphology

Published online by Cambridge University Press:  16 May 2019

Jun Sato ,
Atsuko Kato  and
Naoki Ohashi
Jun Sato
Affiliation:
Department of Pediatric Cardiology, Chukyo Children Heart Center, Japan Community Health Organization Chukyo Hospital, Minami-ku, Nagoya 457-8510, Japan
Atsuko Kato*
Affiliation:
Department of Pediatric Cardiology, Chukyo Children Heart Center, Japan Community Health Organization Chukyo Hospital, Minami-ku, Nagoya 457-8510, Japan
Naoki Ohashi
Affiliation:
Department of Pediatric Cardiology, Chukyo Children Heart Center, Japan Community Health Organization Chukyo Hospital, Minami-ku, Nagoya 457-8510, Japan
*
Author for correspondence: Atsuko Kato, Department of Pediatric Cardiology, Chukyo Children Heart Center, Japan Community Health Organization Chukyo Hospital, 1-1-10 Sanjo, Minami-ku, Nagoya 457-8510, Japan. Tel: +81-52-691-7151; E-mail: [email protected]
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Abstract

Isolation of the left innominate artery from the right aortic arch is a rare anomaly. Herein, we present an even rarer case of incomplete isolation of the proximal left innominate artery with the right aortic arch in a 3-month-old female infant with a double-outlet right ventricle and pulmonary stenosis. Surgical repair at 6 months of age was successful, leading to the restoration of adequate flow in the left arm.

Keywords

Incomplete regressionleft innominate arteryaortic arch anomaly
Type
Brief Report
Information
Cardiology in the Young , Volume 29 , Issue 5 , May 2019 , pp. 717 - 719
Copyright
© Cambridge University Press 2019 

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References

Paul, MW. Aortic arch anomalies. In: Hugh, DA, David, JD, Robert, ES, Timothy, FF (eds.) Moss and Adams’ heart disease in infants, children, and adolescents: including the fetus and young adult, 7th edn. Lippincott Williams and Wilkins, Philadelphia, 2008: 747–748.Google Scholar
Edwards, JE. Anomalies of derivatives of the aortic arch systems. Med Clin North Am 1948; 19: 925–994.CrossRefGoogle Scholar
Kreeger, J, Schlosser, B, Sallee, D, et al. Isolated innominate artery from the main pulmonary artery in DiGeorge syndrome. J Am Coll Cardio 2011; 57: 753 CrossRefGoogle ScholarPubMed
Gowda, SLG, Bhat, PS, Jayaranganath, M, et al. Isolated left brachiocephalic trunk arising from the main pulmonary artery with right aortic arch. J Thorac Cardiovasc Surg 2014; 147: 822–823.CrossRefGoogle Scholar
Dubey, G, Gupta, SK, Kothari, SS, et al. Isolated left brachiocephalic artery with the right aortic arch: a rare differential of large patent ductus arteriosus. Ann Pediatr Cardiol 2017; 10: 78–81.CrossRefGoogle ScholarPubMed
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
Singh, B, Satyapal, KS, Moodley, J, Rajaruthnam, P. Right aortic arch with isolated left brachiocephalic artery. Clin Anat 2001; 14: 47–51.3.0.CO;2-6>CrossRefGoogle ScholarPubMed
Lee, C, Kim, TS, Lee, CH, Kim, SJ. Incomplete isolation of the left innominate artery in a patient with right aortic arch and double outlet right ventricle. J Card Surg 2010; 25:232–234.CrossRefGoogle Scholar

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