| Literature DB >> 22232727 |
Pegah Bronoosh1, Ali Reza Shakibafar, Maneli Houshyar, Shima Nafarzade.
Abstract
Gorlin-Goltz syndrome is an infrequent multi-systemic disease which is characterized by multiple keratocysts in the jaws, calcification of falx cerebri, and basal cell carcinomas. We report a case of Gorlin-Goltz syndrome in a 23-year-old man with emphasis on image findings of keratocyctic odontogenic tumors (KCOTs) on panoramic radiograph, computed tomography, magnetic resonance (MR) imaging, and Ultrasonography (US). In this case, pericoronal lesions were mostly orthokeratinized odontogenic cyst (OOC) concerning the MR and US study, which tended to recur less. The aim of this report was to clarify the characteristic imaging features of the syndrome-related keratocysts that can be used to differentiate KCOT from OOC. Also, our findings suggested that the recurrence rate of KCOTs might be predicted based on their association to teeth.Entities:
Keywords: Gorlin-Goltz syndrome; Magnetic Resonance Imaging; Tomography, X-Ray Computed; Ultrasonography
Year: 2011 PMID: 22232727 PMCID: PMC3251791 DOI: 10.5624/isd.2011.41.4.171
Source DB: PubMed Journal: Imaging Sci Dent ISSN: 2233-7822