| Literature DB >> 36032594 |
Aikaterini D Lianou1, Theodora Martini2, Konstantinos Tsimos3, Athina Zarachi4, Ioannis Kastanioudakis4, Mairi Mouselimi2.
Abstract
Fibrous dysplasia (FD) is a rare, benign, chronic, slowly progressive bone disorder characterized by the replacement of normal bone and bone marrow by fibrous tissue, leading to deformity, pain and functional impairment. It was considered a disease of unknown etiology, uncertain pathogenesis and diverse histopathology. It was later discovered that was caused by a non-heritable activating mutation in the á-subunit gene of the stimulatory G-protein coding gene. Temporal bone involvement is the least frequently reported type, especially in children. The purpose of the current manuscript was to report a rare case of fibrous dysplasia of the left temporal bone of a 17-year-old child who came to the emergency room of our hospital with otalgia and progressive hearing loss on the left ear.Entities:
Year: 2022 PMID: 36032594 PMCID: PMC9375899 DOI: 10.26574/maedica.2022.17.2.524
Source DB: PubMed Journal: Maedica (Bucur) ISSN: 1841-9038