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Echocardiographic diagnosis of left carotid artery arising from the pulmonary trunk

Published online by Cambridge University Press:  15 January 2008

Viktor Tomek*
Affiliation:
Kardiocentrum and Cardiovascular Research Centre, University Hospital Motol, Prague, Czech Republic
Oleg Reich
Affiliation:
Kardiocentrum and Cardiovascular Research Centre, University Hospital Motol, Prague, Czech Republic
Jan Skovranek
Affiliation:
Kardiocentrum and Cardiovascular Research Centre, University Hospital Motol, Prague, Czech Republic
*
Kardiocentrum and Cardiovascular Research Centre, University Hospital Motol, V uvalu 84, 150 08 Prague 5, Czech Republic. Tel: +420 22443 2900; Fax: +420 22443 2915; E-mail: viktor.tomek@seznam.cz
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Abstract

Type
Images in Congenital Cardiac Disease
Copyright
Copyright © Cambridge University Press 2008

A three-week-old male with choanal atresia and CHARGE association was referred for evaluation of a systolic murmur. Echocardiography (Fig. 1) revealed a right aortic arch (RAOA) with aberrant origin of the left subclavian artery (LSA), as well as a large, right-sided patent arterial duct (PDA). An abnormal vessel, arising from the bifurcation of the pulmonary trunk (MPA), and passing to the neck, was identified as the left carotid artery (LCAR). Angiography confirmed the diagnosis (Fig. 2; Abbreviations: LPA = left pulmonary artery, RCAR = right carotid artery, RSA = right subclavian artery). The left carotid artery was translocated to the ascending aorta, and the duct was ligated via midline sternotomy. A left-sided arterial ligament was not observed at the time of surgery.

Figure 1 Echocardiograms from the suprasternal approach. Left: right aortic arch with a huge right sided arterial duct. Right: left carotid artery arising from pulmonary artery bifurcation and aberrant left subclavian artery.

Figure 2 Angiograms in frontal projection. Left: aortography. Right: transductal pulmonary artery injection.

Only 5 cases of this malformation have thus far been reported. Right aortic arch with aberrant left subclavian artery was present in all. The hypothetical system for regression of the arteries of the pharyngeal arches proposed by Edwards not explain this anomaly, nor does an arterial duct connecting the pulmonary and left carotid arteries, as all but one of the described cases had a left-sided duct or ligament separate from the left carotid artery. We propose abnormal formation of the arterial pole of the developing embryo as a more likely explanation. CHARGE association, also present in our patient, is an anomaly of migration of cells from the neural crest. Manner et al.,Reference Manner, Seidl and Stesing1 by ablation of such cells migrating from the neural crest in chicken embryos, have induced abnormal formation of the arterial pole resulting in origin of a left brachiocephalic artery from the pulmonary trunk in association with right aortic arch and aberrant left subclavian artery.

Acknowledgements

The publication was supported by the grant of the Czech Ministry of Health – VZ FNM 64203.

References

1. Manner, J, Seidl, W, Stesing, G. The formal pathogenesis of isolated common carotid or innominate arteries: the concept of malseptation of the aortic sac. Anat Embryol 1997; 196: 435445.Google ScholarPubMed
Figure 0

Figure 1 Echocardiograms from the suprasternal approach. Left: right aortic arch with a huge right sided arterial duct. Right: left carotid artery arising from pulmonary artery bifurcation and aberrant left subclavian artery.

Figure 1

Figure 2 Angiograms in frontal projection. Left: aortography. Right: transductal pulmonary artery injection.