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Published in: Pediatric Radiology 11/2012

01-11-2012 | Original Article

Agenesis of the internal carotid artery: associated malformations including a high rate of aortic and cardiac malformations

Authors: Ryan T. Fitzgerald, Giulio Zuccoli

Published in: Pediatric Radiology | Issue 11/2012

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Abstract

Background

Agenesis of the internal carotid artery (ICA) is a rare congenital anomaly occurring in less than 0.01% of the population, often incidentally discovered in pediatric populations. We recognized a high incidence of additional congenital malformations in children with ICA agenesis.

Objective

Our study reports nine cases of ICA agenesis and co-existent malformations and discusses implications of the association.

Materials and methods

We conducted a retrospective chart review of nine children evaluated at our institution with imaging findings of ICA agenesis.

Results

Seven children (78%) had congenital aortic or cardiac anomalies including coarctation (4), hypoplastic left heart (1), tetralogy of Fallot (1), and muscular ventricular septal defect (VSD) (1). Four children were diagnosed with an inherited disorder: Alagille syndrome (1), PHACE syndrome (1), VACTERL association (1), and methylenetetrahydrofolate reductase (MTHFR) gene variant (1). Additional congenital anomalies are also described.

Conclusion

In the setting of ICA agenesis, we report a robust association with congenital aortic and cardiac anomalies, as well as a broad spectrum of additional anatomical abnormalities that can occur in the setting of known genetic syndromes or as isolated findings. Knowledge of the natural history of ICA agenesis and associated anomalies will guide optimal care for these children.
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Metadata
Title
Agenesis of the internal carotid artery: associated malformations including a high rate of aortic and cardiac malformations
Authors
Ryan T. Fitzgerald
Giulio Zuccoli
Publication date
01-11-2012
Publisher
Springer-Verlag
Published in
Pediatric Radiology / Issue 11/2012
Print ISSN: 0301-0449
Electronic ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-012-2455-6

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