Hostname: page-component-848d4c4894-p2v8j Total loading time: 0.001 Render date: 2024-05-28T06:04:49.270Z Has data issue: false hasContentIssue false
  • English
  • Français

Anomalous origin of the right coronary artery from the pulmonary artery associated with tetralogy of Fallot: description of the pre-surgical diagnosis and surgical repair

Published online by Cambridge University Press:  02 March 2011

Francesca R. Pluchinotta ,
Vladimiro Vida  and
Ornella Milanesi
Francesca R. Pluchinotta
Affiliation:
Pediatric Cardiology Unit, Department of Pediatrics, University of Padua Medical School, Padua, Italy
Vladimiro Vida
Affiliation:
Pediatric and Congenital Cardiac Surgery Unit, Department of Cardiac Surgery, University of Padua Medical School, Padua, Italy
Ornella Milanesi*
Affiliation:
Pediatric Cardiology Unit, Department of Pediatrics, University of Padua Medical School, Padua, Italy
*
Correspondence to: Professor O. Milanesi, MD, Pediatric Cardiac Unit, Department of Pediatrics, University of Padua Medical School, Via Giustiniani no. 3, 35128 Padova, Italy. Tel: +39 49 8211400; Fax: +39 49 8218089; E-mail: ornella.milanesi@unipd.it
Get access Rights & Permissions [Opens in a new window]

Abstract

Anomalous origin of the right coronary artery from the pulmonary artery is a rare congenital defect. We describe the case of an infant with anomalous origin of the right coronary artery from the pulmonary artery in association with tetralogy of Fallot. This patient had a pre-operative echocardiographic diagnosis, which was confirmed by angiography, and later underwent a successful surgical repair.

Keywords

Congenital cardiac diseaseechocardiographycardiovascular surgical procedures
Type
Brief Reports
Information
Cardiology in the Young , Volume 21 , Issue 4 , 12 July 2011 , pp. 468 - 470
Copyright
Copyright © Cambridge University Press 2011

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

1.Kühn, A, Kasnar-Samprec, J, Schreiber, C, Vogt, M. Anomalous origin of the right coronary artery from the pulmonary artery. Int J Cardiol 2010; 139: e27–e28.CrossRefGoogle ScholarPubMed
2.Bossert, T, Walther, T, Doll, N, Gummert, JF, Kostelka, M, Mohr, FW. Anomalous origin of the right coronary artery from the pulmonary artery combined with aortic valve stenosis. Ann Thorac Surg 2005; 79: 347–348.CrossRefGoogle ScholarPubMed
3.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.e9–1004.e17.CrossRefGoogle Scholar
4.Su, JT, Krishnamurthy, R, Chung, T, Vick, GW 3rd, Kovalchin, JP. Anomalous right coronary artery from the pulmonary artery: noninvasive diagnosis and serial evaluation. J Cardiovasc Magn Reson 2007; 9: 57–61.CrossRefGoogle ScholarPubMed
5.Moss, RL, Backer, CL, Zales, VR, Florentine, MS, Mavroudis, C. Tetralogy of Fallot with anomalous origin of the right coronary artery. Ann Thorac Surg 1995; 59: 229–231.CrossRefGoogle ScholarPubMed
6.Coe, JY, Radley-Smith, R, Yacoub, M. Clinical and hemodynamic significance of anomalous origin of the right coronary artery from the pulmonary artery. Thorac Cardiovasc Surg 1982; 30: 84–87.CrossRefGoogle ScholarPubMed
7.Meng, CC, Eckner, FA, Lev, M. Coronary artery distribution in tetralogy of Fallot. Arch Surg 1965; 90: 363–366.CrossRefGoogle ScholarPubMed
8.Ranniger, K, Thilenius, OG, Cassels, DE. Angiographic diagnosis of an anomalous right coronary artery arising from the pulmonary artery. Radiology 1967; 88: 29–31.CrossRefGoogle ScholarPubMed