Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-27T09:37:24.939Z Has data issue: false hasContentIssue false

Anomalous origin of a single coronary artery from the pulmonary artery associated with patent ductus arteriosus

Published online by Cambridge University Press:  08 June 2020

Nicolas Hugues*
Affiliation:
Centre Cardio-Thoracique de Monaco, Monaco, Monaco
Carine Dommerc
Affiliation:
Centre Cardio-Thoracique de Monaco, Monaco, Monaco
René Pretre
Affiliation:
Centre Cardio-Thoracique de Monaco, Monaco, Monaco Service de Chirurgie Cardiaque, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
*
Author for correspondence: Nicolas Hugues, Centre Cardio-Thoracique de Monaco, 98000 Monaco, Monaco. Tel: +377 92168211; Fax: +377 93254382. E-mail: nhugues@ccm.mc

Abstract

We report an unusual case of a 12-month-old boy diagnosed with anomalous origin of a single coronary artery from the pulmonary artery associated with patent ductus arteriosus. The patient survival was attributed to left-to-right shunt (patent ductus arteriosus) allowing for appropriate myocardial perfusion. Successful surgical correction involved patent ductus arteriosus closure, mitral annuloplasty and reimplantation of the coronary artery into the aortic root.

Type
Brief Report
Copyright
© The Author(s), 2020. 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

Tavora, F, Burke, A, Kutys, R, Li, L, Virmani, R.Total anomalous origin of the coronary circulation from the right pulmonary artery. Cardiovasc Pathol 2008; 17: 246249.CrossRefGoogle ScholarPubMed
Keith, JD.The anomalous origin of the left coronary artery from the pulmonary artery. Br Heart J 1959; 21: 149161.CrossRefGoogle ScholarPubMed
Williams, IA, Gersony, WM, Hellenbrand, WE.Anomalous right coronary artery arising from the pulmonary artery: a report of 7 cases and a review of the literature. Am Heart J 2006; 152: 1004.e91004.e17.CrossRefGoogle Scholar
Kawamura, A, Oshima, Y, Maruo, A, Matsuhisa, H.Compression of an anomalous single coronary artery from pulmonary artery by banding. Eur J Cardiothorac Surg 2012; 41: e59e61.CrossRefGoogle ScholarPubMed
Karimi, M, Hulsebus, E, Lutin, W.Reimplantation of anomalous single coronary artery from pulmonary artery: diagnosis and surgical management. Ann Thorac Surg 2012; 93: 308310.CrossRefGoogle ScholarPubMed
Heifetz, SA, Robinowitz, M, Mueller, KH, Virmani, R.Total anomalous origin of the coronary arteries from the pulmonary artery. Pediatr Cardiol 1986; 7: 1118.CrossRefGoogle ScholarPubMed
Santoro, G, di Carlo, D, Carotti, A, et al.Origin of both coronary arteries from the pulmonary artery and aortic coarctation. Ann Thorac Surg 1995; 60: 706708.CrossRefGoogle ScholarPubMed
Monselise, MB, Vlodaver, Z, Neufeld, HN.Single coronary artery: origin from the pulmonary trunk in association with ventricular septal defect. Chest 1970; 58: 613616.CrossRefGoogle ScholarPubMed
D’Alessandro, LC, Di Lorenzo, M. [Single coronary artery originating from the left pulmonary artery of a “truncus arteriosus communis” in a living 39 year-old-patient (author’s transl). G Ital Cardiol 1976; 6: 939945.Google Scholar
Feldt, RH, Ongley, PA, Titus, JL.Total coronary arterial circulation from pulmonary artery with survival to age seven: report of case. Mayo Clin Proc 1965; 40: 539543.Google Scholar