Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study
Wójcik Sylwia,
Koszowski Rafał,
Drozdowska Bogna,
Śmieszek-Wilczewska Joanna,
Raczkowska-Siostrzonek Agnieszka
Affiliations
Wójcik Sylwia
Chair of Dental Surgery, Department of Cranio-Maxillofacial Surgery and Oral Surgery, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Poland
Koszowski Rafał
Chair of Dental Surgery, Department of Cranio-Maxillofacial Surgery and Oral Surgery, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Poland
Drozdowska Bogna
Chair of Pathomorphology, Medical University of Silesia in Katowice, Poland
Śmieszek-Wilczewska Joanna
Chair of Dental Surgery, Department of Cranio-Maxillofacial Surgery and Oral Surgery, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Poland
Raczkowska-Siostrzonek Agnieszka
Chair of Dental Surgery, Department of Cranio-Maxillofacial Surgery and Oral Surgery, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Poland
McCune Albright syndrome (MCA) is a rare complication of genetic origin. The authors present a case study of a patient with MCA diagnosed with multifocal fibrous dysplasia in his limb and craniofacial bones. The symptoms of the disease in the patient’s facial and oral tissue and the treatment administered have been described.
