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Congenital Vomer Agenesis: A Rare and Poorly Understood Condition Revealed by Cone Beam CT
David Jun Yan1, Vincent Lenoir2, Sibylle Chatelain3
1Department of Imaging and Informatics Sciences, Division of Radiology, University Hospital Geneva, University of Geneva, 1211 Geneva, Switzerland. DavidJun.Yan@hcuge.ch.
Abstract:
Isolated congenital vomer agenesis is a very rare and poorly understood condition. In the context of dental work-up by cone-beam computed tomography (CBCT), the explored volume of the facial bones occasionally reveals incidental abnormalities. We report the case of a 13-year old Caucasian female who underwent CBCT for the pre-treatment evaluation of primary failure of tooth eruption affecting the permanent right upper and inferior molars. CBCT depicted a large defect of the postero-inferior part of the nasal septum without associated soft tissue abnormality and without cranio-facial malformation or cleft palate. In the absence of a history of trauma, chronic inflammatory sinonasal disease, neoplasia and drug abuse, a posterior nasal septum defect warrants the diagnosis of vomer agenesis. A discussion of this condition and of salient CBCT features is provided.
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