Key Points
■ Plain skull radiography demonstrates moderate to high sensitivity and specificity in craniosynostosis.
■ Numerous publications support 3D-CT as the imaging modality with the best diagnostic performance, with reported sensitivities of 96–100%. CT also detects associated intracranial pathology.
■ Higher diagnostic performance is obtained with plain films and CT if the studies are of good quality and interpreted by an experienced reviewer.
■ Cranial sonography shows preliminary promise as a diagnostic test for craniosynostosis. The evidence is based on small cohorts; hence, larger series are needed before it is routinely used.
■ Imaging strategies for children with suspected craniosynostosis should be based on their risk group. In healthy children with head deformity including posterior plagiocephaly, skull radiography is recommended. Syndromes such as Apert, Crouzon, and Pfeiffer nearly always have associated craniosynostosis and hence require 3D imaging for surgical planning.
■ Imaging is not necessary for diagnosis or preoperative planning in isolated craniosynostosis with unequivocal clinical findings. However, in countries with high medicolegal issues, imaging may still be required.
■ Intracranial anomalies can be seen in some patients with craniosynostosis but the exact incidence is not well known.
■ Small retrospective US and MRI studies demonstrate the feasibility of prenatal diagnosis of craniosynostosis. However, large prospective studies are still required to understand the prenatal role of imaging in craniosynostosis and their effect on postnatal outcome.
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Vinocur, D.N., Medina, L.S. (2010). Imaging in the Evaluation of Children with Suspected Craniosynostosis. In: Medina, L., Applegate, K., Blackmore, C. (eds) Evidence-Based Imaging in Pediatrics. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-0922-0_4
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