Hostname: page-component-74656f9884-8r8nv Total loading time: 0 Render date: 2026-11-07T01:07:09.144Z Has data issue: false hasContentIssue false
  • English
  • Français

Aortic coarctation, aneurysm, and ventricular dysfunction in an asymptomatic infant

Published online by Cambridge University Press:  16 March 2016

Ana I. García ,
Juan M. Aguilar  and
Enrique García
Ana I. García
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
Juan M. Aguilar*
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
Enrique García
Affiliation:
Department of Pediatric Cardiac Surgery, Pediatric Heart Institute, Hospital Universitario Doce de Octubre, Madrid, España
*
Correspondence to: J. M. Aguilar, Avenida de Córdoba s/n, 28041 Madrid, Spain. Tel: +34 917 390 8508; Fax: +34 917 390 8772; E-mail: juanmiccv@gmail.com
Rights & Permissions [Opens in a new window]

Abstract

Aortic arch coarctation with post-coarctation aneurysm is rare in infants. We present the case of an asymptomatic 3-month-old infant with severe left ventricular dysfunction in this setting. The patient underwent surgical repair, and the left ventricular ejection fraction improved to recovery the 4th post-operative month.

Keywords

Aortacoarctationaneurysm

Information

Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 26 , Issue 5 , June 2016 , pp. 971 - 972
Check for updates
Copyright
© Cambridge University Press 2016 

We present the case of an asymptomatic 3-month-old girl in whom a heart murmur and decreased femoral pulses were noted incidentally during a routine medical examination. The two-dimensional echocardiography revealed tricuspid aortic valve, left aortic arch, severe distal aortic arch coarctation with post-coarctation aneurysmReference Ozyuksel, Canturk and Dindar 1 about 2 cm in diameter, and severe left ventricular dysfunction (<30%). The ductus arteriosus was patent, joined to the aneurysm with right-to-left shunt. The three-dimensional CT-scan confirmed these findings and showed the left subclavian artery emerging distal to the aneurysm with reverse flow perfusing the descending aorta (Fig 1a and b) and right subclavian artery normally arising from the innominate artery, although with anomalous initial course – double corkscrew.

Figure 1

Three-dimensional CT scan images. ( a ) The white arrow shows the aortic arch coarctation. ( b ) The white arrow shows the left subclavian artery emerging distal to the aneurysm.

Surgical repair was performed through a median sternotomy with the patient under cardiopulmonary bypass, moderate hypothermia, and selective cerebro-myocardial perfusion (Fig 2a). The ductus arteriosus was ligated. The aneurysm and the coarcted segment were resected (Fig 2b). Extended end-to-end anastomosis with fresh autologous pericardial patch augmentation was performed (Fig 3a). Diffuse thickening of the aortic wall was observed, but any type of vasculitis including PHACE syndromeReference Bayer, Frommelt and Blei 2 was ruled out with analytical, physical, and histopathological examinations.

Figure 2

( a ) Intraoperative view before repair. ( b ) Surgical specimen with diffuse thickening of the aortic wall. AA=aortic aneurysm; DA=ductus arteriosus divided; DAA=distal aortic arch; LCA=left carotid artery.

Figure 3

( a ) Intraoperative view after repair. The white arrow shows the autologous pericardial patch. ( b ) Post-operative MRI showing the reconstructed aortic arch.

Post-operative echocardiography showed a normal reconstructed aortic arch with no residual gradient. Post-operative MRI (Fig 3b) showed the reconstructed aortic arch with no defects in myocardial viability. The left ventricular ejection fraction improved to recovery the 4th post-operative month.

Acknowledgement

None.

Financial Support

This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.

Conflicts of Interest

None.

References

1. Ozyuksel, A, Canturk, E, Dindar, A, et al. Saccular aneurysm formation of the descending aorta associated with aortic coarctation in an infant. Rev Bras Cir Cardiovasc 2014; 29: 642–644.Google ScholarPubMed
2. Bayer, ML, Frommelt, PC, Blei, F, et al. Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry). Am J Cardiol 2013; 112: 1948–1952.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1 Three-dimensional CT scan images. (a) The white arrow shows the aortic arch coarctation. (b) The white arrow shows the left subclavian artery emerging distal to the aneurysm.

Figure 1

Figure 2 (a) Intraoperative view before repair. (b) Surgical specimen with diffuse thickening of the aortic wall. AA=aortic aneurysm; DA=ductus arteriosus divided; DAA=distal aortic arch; LCA=left carotid artery.

Figure 2

Figure 3 (a) Intraoperative view after repair. The white arrow shows the autologous pericardial patch. (b) Post-operative MRI showing the reconstructed aortic arch.