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- W2892500987 abstract "A 13-year-old boy presented with mandibular swelling. Extraoral examination revealed facial asymmetry, inflammatory lymphadenopathy, and polydactyly in both hands and feet. Panoramic radiography showed a well-delimited, radiolucent lesion on the left mandible. Sprengel deformity and mild thoracic defect were observed with conventional radiography. Skin showed no basal cell carcinoma. The clinical hypothesis included odontogenic keratocyst and ameloblastoma. Incisional biopsy revealed a cyst lined with parakeratinized epithelium. The basal layer cells were columnar, palisaded, and hyperchromatic, features compatible with odontogenic keratocyst. Gorlin-Goltz syndrome was considered according to 1 major and 3 minor criteria, odontogenic keratocyst, Sprengel deformity, mild thorax deformity, and defective hands and feet, respectively. Cystic decompression was performed. The patient remains under follow-up care, with significant lesion decrease and bone neoformation. Enucleation will be conducted later. Diagnosis of Gorlin-Goltz syndrome is challenging, given the varied forms of presentation. Careful investigation should be performed." @default.
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- W2892500987 date "2018-09-01" @default.
- W2892500987 modified "2023-09-27" @default.
- W2892500987 title "Gorlin-Goltz Syndrome: A Case Report of A Young Patient" @default.
- W2892500987 doi "https://doi.org/10.1016/j.oooo.2018.02.163" @default.
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