Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/8430
Title: The surgical management of gardner syndrome manifestation in the maxillofacial region: A case report
Authors: Loncarevic, Slobodan
Brajkovic D.
Popovic M.
Gardasevic M.
Sekulic, Miona
Matejic, Suzana
Journal: Serbian Journal of Experimental and Clinical Research
Issue Date: 1-Jan-2019
Abstract: © 2019, University of Kragujevac, Faculty of Science. All rights reserved. Gardner syndrome is a rare autosomal-dominant genetic disorder, considered a variant of familial adenomatous polyposis. It is characterized by intestinal polyposis and various bone and soft-tissue tumors, including osteomas, epidermal and dermal cysts, lipomas and fibromas. Intestinal polyps have high potential to become malignant, and the screening of intestinal lesions is mandatory. Maxillofacial manifestations, such as jaw osteomas, odontomas, dental abnormalities and soft tissue tumors frequently precede the intestinal manifestations. Thus, maxillofacial surgeons and dental practitioners may have important role in early detection of Gardner syndrome. In this case report we present a 22 year old male patient who was reffered to maxillofacial surgeon due to osteoma of the mandible. After obtaining clinical and radiological examinations, as well as data from family history, Gardner syndrome was suspected, which was later confirmed after gastroenterological examination.
URI: https://scidar.kg.ac.rs/handle/123456789/8430
Type: article
DOI: 10.1515/SJECR-2017-0038
ISSN: 18208665
SCOPUS: 85070452555
Appears in Collections:Faculty of Medical Sciences, Kragujevac

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