Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-19T04:34:42.833Z Has data issue: false hasContentIssue false

Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect

Published online by Cambridge University Press:  19 December 2011

Poay Huan Loh*
Affiliation:
Rigshospitalet University Hospital, Copenhagen, Denmark Hull and East Yorkshire Hospitals NHS Trust, Hull, United Kingdom
Tim Jensen
Affiliation:
Rigshospitalet University Hospital, Copenhagen, Denmark
Lars Søndergaard
Affiliation:
Rigshospitalet University Hospital, Copenhagen, Denmark
*
Correspondence to: Dr L. Søndergaard, Rigshospitalet University Hospital, Blegdamsvej 9, Copenhagen 2100, Denmark. Tel: +45 35452018; Fax: +45 35452705; E-mail: [email protected]

Abstract

Congenital aortocaval fistula is a very rare anomaly. Clinically, it resembles conditions that cause left-to-right shunt of blood. We report a case of such anomaly in combination with a secundum atrial septal defect in a 13-month-old girl who presented with failure to thrive and exertional respiratory symptoms. The aortocaval fistula was occluded percutaneously using an Amplatzer® Duct Occluder.

Type
Brief Report
Copyright
Copyright © Cambridge University Press 2012

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. Soler, P, Mehta, AV, Garcia, OL, Kaiser, G, Tamer, D. Congenital systemic arteriovenous fistula between the descending aorta, azygos vein, and superior vena cava. Chest 1981; 80: 647649.CrossRefGoogle ScholarPubMed
2. Oomman, A, Mao, R, Krishnan, P, Girinath, MR. Congenital aortocaval fistula to the superior vena cava. Ann Thorac Surg 2001; 72: 911913.CrossRefGoogle Scholar
3. Antunes, A, Marhino, A, Rodrigues, D, Melo, A, Oliveira, L, Providencia, LA. Percutaneous embolization of a congenital aortocaval fistula – clinical case. Rev Port Cardiol 2003; 22: 11011106.Google ScholarPubMed
4. Rosenberg, H, Williams, WG, Trusler, GA, et al. Congenital aortico-right atrial communications. The dilemma of differentiation from coronary-cameral fistula. J Thorac Cardiovasc Surg 1986; 91: 841847.CrossRefGoogle ScholarPubMed
5. Coto, EO, Caffarena, JM, Such, M, Marques, JL. Aorta – right atrial communication. Report of an unusual case. J Thorac Cardiovasc Surg 1980; 80: 941944.CrossRefGoogle ScholarPubMed
6. Perry, SB, Rome, J, Keane, JF, Baim, DS, Lock, JE. Transcatheter closure of coronary artery fistulas. J Am Coll Cardiol 1992; 20: 205209.CrossRefGoogle ScholarPubMed
7. Awasthy, N, Tomar, M, Radhakrishnan, S, Kumar, P. Nonsurgical management of a congenital aortocaval fistula from right subclavian artery to superior vena cava along with SVC obstruction. Pediatr Cardiol 2011; 32: 227229.CrossRefGoogle ScholarPubMed
8. Wong, CK, Lau, CP, Leung, WH. An arteriovenous fistula from an aberrant right subclavian artery to the superior caval vein in a congenitally myxoedematous adult. Int J Cardiol 1989; 25: 126129.CrossRefGoogle Scholar
9. Auge, JM, Bosch, X, Crexells, C, Oriol, A. Subclavian artery to pulmonary circulation fistulas. Cathet Cardiovasc Diagn 1983; 9: 175180.CrossRefGoogle ScholarPubMed
10. Gutierrez, FR, Monaco, MP, Hartmann, AF Jr, McKnight, RC. Congenital arteriovenous malformations between brachiocephalic arteries and systemic veins. Chest 1987; 92: 897899.CrossRefGoogle ScholarPubMed