Craniofacial fibrous dysplasia: A case report and literature review

Abstract

Fibrous dysplasia (FD) is a rare osseous pathology of unknown origin in which normal bone is replaced by fibro-osseous tissue. Recent research has linked FD to a somatic mutation in the protein transcription of the GNAS1 gene, which leads to an increase in intracellular cyclic adenosine monophosphate. FD represents 3% of all bony tumors and over 7% of all non-malignant bone tumors. FD has various clinical presentation groups such as the monostotic, craniofacial and polyostotic forms, and the McCune-Albright syndrome. We present a craniofacial FD case of a 45-year-old female patient, who underwent surgical treatment many times.

Priority of treatment in craniofacial fibrous dysplasia

“…[3] It is caused by somatic-activating mutations encoded by the gene GNAS in the α subunit of the stimulating G protein. [3456] It has the potential to cause cosmetic and functional disturbance. Ocular effects are of particular concern.…”