Hostname: page-component-74656f9884-skzmx Total loading time: 0 Render date: 2026-11-06T01:03:00.721Z Has data issue: false hasContentIssue false
  • English
  • Français

Tetralogy of Fallot with double aortic arch

Published online by Cambridge University Press:  26 July 2011

Andrew Robert Harper ,
Monica Dai  and
Rashmi M. Prabhatha
Andrew Robert Harper*
Affiliation:
Institute of Genetic Medicine, Newcastle University, Institute of Medical Sciences, Newcastle Upon Tyne, United Kingdom
Monica Dai
Affiliation:
Department of Medical Sciences, Queen's University, Kingston, Ontario, Canada
Rashmi M. Prabhatha
Affiliation:
Paediatric Cardiothoracic Surgery, Narayana Hrudayalaya, Bangalore, Karnataka, India
*
Correspondence to: A. R. Harper, Institute of Genetic Medicine, Newcastle University, Institute of Medical Sciences, Newcastle Upon Tyne, NE1 3BZ, United Kingdom. E-mail: A.r.harper@ncl.ac.uk
Rights & Permissions [Opens in a new window]

Abstract

An 8 year old girl presents with cyanosis, exertional dyspnoea, and palpitation only. X-ray displayed a typical coeur en sabot heart and auscultsation revealed a harsh ejection systolic murmur. Echocardiography confirmed Tetralogy of Fallot (McGoon ratio 1.3) and computed tomography was requested for further investigation of pulmonary stenosis. A vascular ring was detected, presenting asymptomatically and previously missed through echocardiography. The patient underwent a double-stage repair with ligation of an aortic arch. Recovery was unremarkable. This case highlights the limitations of echocardiography in detection of extra-cardiac anomalies.

Keywords

Asymptomatic double aortic archvascular ringTetralogy of Fallotpaediatric congenital heart disease

Information

Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 21 , Issue 6 , 28 October 2011 , pp. 695 - 696
Copyright
Copyright © Cambridge University Press 2011

The following report describes the detection of an asymptomatic double aortic arch within a patient with Tetralogy of Fallot within a tertiary referral centre.

Case report

An 8-year-old North Indian girl presented with cyanosis, exertional dyspnoea, and palpitation only. Following clinical examination of the child – 122 centimetres, 20 kilograms, 96 beats per minute, pulse oximeter oxygen saturation 73% on air – a harsh 3/6 ejection systolic murmur was detected in the third right intercostal space, with an electrocardiogram reporting right-axis deviation and early R-wave transition. The X-ray displayed a typical coeur en sabot heart, pulmonary bay accentuation, and oligaemic lung fields.

Investigation

The echocardiography confirmed the diagnosis of Tetralogy of Fallot consisting of a 12.2-millimetre bidirectional perimembranous ventricular septal defect, infundibular pulmonary artery stenosis, with a gradient of 84 millimetres of mercury, and both right atrial and ventricular dilation with a McGoon ratio of 1.3. Computed tomography was requested to further analyse the pulmonary artery stenosis; however, a coincidental finding of a double aortic arch was detected following the echocardiography, which confirmed Tetralogy of Fallot. The vascular ring presented asymptomatically and was undetected through echocardiographic investigation. Both aortic arches displayed relatively equal patency. No cytogenetic analysis was conducted.

Intervention

The patient underwent a double-stage repair through a left thoracotomy for the ligation of the posterior aortic arch, followed by a modified Blalock–Taussig shunt through the insertion of a 5-millimetre polytetrafluoroethylene tube, anastamosing the left subclavian artery to the left pulmonary artery. Postoperatively, the patient was haemodynamically stable and recovery was unremarkable.

Figure 1

Three dimensional computed tomography image of double aortic arch. Original source from Narayana Hrudayalaya Department of Radiology.

Discussion

Asymptomatic double aortic arches combined with Tetralogy of Fallot in an 8-year-old are incredibly rare. Aortic arch anomalies comprise 1 per cent of operable congenital cardiac disease. This case highlights the limitations of echocardiography in the detection of extra-cardiac anomalies.

Figure 0

Figure 1 Three dimensional computed tomography image of double aortic arch. Original source from Narayana Hrudayalaya Department of Radiology.