Abstract
Aorto–right atrial tunnel (ARAT) is a rare clinical entity. Although it is a benign finding in most cases; it can present with significant right ventricular volume overload and congestive heart failure. This report describes the first fetal diagnosis of congenital aorto–right atrial tunnel and successful management of the heart failure by surgical intervention.
Similar content being viewed by others
References
Akar RA, Şırlak M, Eyileten Z et al (2006) Aortico-cameral communication from right sinus of Valsalva to right atrium. Ankara Üniversitesi Týp Fakültesi Mecmuasý 59:73–76
Coto EO, Caffarena JM, Such M et al (1980) Aorta–right atrial communication: report of an unusual case. J Thorac Cardiovasc Surg 80:941–944
Danilowicz D, Presti S, Colvin S et al (1989) Congenital fistulous tract between aorta and right atrium presenting as heart failure in a newborn. Pediatr Cardiol 10:93–97
Sivakumar K, Shahani JM, Francis E (2006) Transcatheter closure of aortico right atrial tunnel: a rare cardiac anomaly. Congenit Heart Dis 1:324–326
Tanaka T, Tomita H, Watanabe K et al (2005) A case of aorto–right atrial tunnel associated with aortic and tricuspid atresia. Pediatr Int 47:466–468
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Deshpande, S.R., Fyfe, D.A. Aorto–Right Atrial Tunnel: Fetal Heart Failure, Diagnosis, and Treatment. Pediatr Cardiol 31, 299–300 (2010). https://doi.org/10.1007/s00246-009-9567-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00246-009-9567-2