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The closing process of the ductus arteriosus connecting the left common carotid artery and main pulmonary artery

Published online by Cambridge University Press:  11 February 2019

Kumiyo Matsuo
Affiliation:
Department of Pediatric Cardiology, Osaka Women’s and Children’s Hospital, Osaka, Japan
Hisaaki Aoki*
Affiliation:
Department of Pediatric Cardiology, Osaka Women’s and Children’s Hospital, Osaka, Japan
Futoshi Kayatani
Affiliation:
Department of Pediatric Cardiology, Osaka Women’s and Children’s Hospital, Osaka, Japan
*
Author for correspondence: H. Aoki, MD, PhD, Department of Pediatric Cardiology, Osaka Women’s and Children’s Hospital, Osaka, Japan, 840 Murodocho Izumi City, Osaka 594-1101, Japan. Tel: +81 725 56 1220; Fax: +81 725 56 5682; E-mail: [email protected]

Abstract

An isolated left common carotid artery is very rare, and only 13 cases have been reported thus far. All those cases were accompanied by a right aortic arch and aberrant left subclavian artery, and the connecting vessel between the pulmonary artery and left common carotid artery was thought to be ductal tissue. However, there have been no reports that have followed the natural closure of this vessel. We present a case in whom we could observe the closing process of this vessel at the connection between the left common carotid artery and main pulmonary artery in association with a tetralogy of Fallot.

Type
Brief Report
Copyright
© Cambridge University Press 2019 

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Footnotes

Cite this article: Matsuo K, Aoki H, Kayatani F. (2019) The closing process of the ductus arteriosus connecting the left common carotid artery and main pulmonary artery. Cardiology in the Young29: 422–424. doi: 10.1017/S1047951118002275

References

1. Fong, LV, Venables, AW. Isolation of the left common carotid or left innominate artery. Br Heart J 1987; 57: 552554.Google Scholar
2. Fouilloux, V, Gran, C, Kreitmann, B. Isolated left common carotid artery connected to the pulmonary artery: where was the arterial duct? World J Pediatr Congenit Heart Surg 2013; 4: 229232.Google Scholar
3. Manner, J. Isolated left common carotid artery arising from the main pulmonary artery: where is the ductus arteriosus? An embryologist’s view. World J Pediatr Congenit Heart Surg 2013; 4: 460461.Google Scholar
4. Osakwe, O, Jones, B, Hirsch, R. Anomalous origin of the left common carotid artery from the main pulmonary artery: a rare association in an infant with CHARGE syndrome. Case Rep Pediatr 2016; 2016: 2064937.Google Scholar
5. Gil-Jaurena, JM, Ferreiros, M, Zabala, I, Cuenca, V. Right aortic arch with isolation of the left innominate artery arising from the pulmonary artery and atrial septal defect. Ann Thorac Surg 2011; 91: 303.Google Scholar
6. Idhrees, AM, Mathew, T, Menon, S, Dharan, BS, Jayakumar, K. A shunt from the brain: left internal carotid artery arising from the left pulmonary artery in tetralogy of Fallot. Ann Thorac Surg 2015; 99: e47e49.Google Scholar
7. Kaushik, N, Saba, Z, Rosenfeld, H, et al. An isolated left common carotid artery from the main pulmonary artery: possible malseptation of the truncoaortic sac. Pediatr Cardiol 2005; 26: 707709.Google Scholar
8. Ahmadi, A, Sabri, M, Dehghan, B. An isolated left common carotid artery from the main pulmonary artery in a neonate with aortic valve atresia. Cardiol Young 2015; 25: 11931196.Google Scholar
9. Oppido, G, Pace Napoleone, C, Gabbieri, D, et al. Images in cardiovascular medicine. Left common carotid artery isolation in a newborn with tetralogy of Fallot and DiGeorge syndrome. Circulation 2005; 111: e4e5.Google Scholar