Two Cases of Temporomandibular Synovial Chondromatosis Associated with Gli1 Gene Mutation

Int J Environ Res Public Health. 2022 Apr 13;19(8):4702. doi: 10.3390/ijerph19084702.

Abstract

Synovial chondromatosis (SC) is a rare benign disease involving multifocal generation of ectopic cartilage in the synovial tissue. Herein, we report two cases of SC in the temporomandibular joint: a 38-year-old woman (patient 1) and 39-year-old woman (patient 2). Both patients had trismus, jaw joint noises, and jaw-opening pain in the temporomandibular joint. Cone-beam computed tomography (CT) and magnetic resonance imaging (MRI) in patient 1 showed multiple calcified loose bodies around the right mandibular condyle. In addition, CT and MRI in patient 2 showed multiple calcified loose bodies around the left mandibular condyle and temporal bone perforation. Following establishing a diagnosis of SC, both patients underwent tumor resection via open surgery. In immunohistochemical examinations of the resected tissues, tumor cells showed intense nuclear staining with labeled anti-Gli1 antibody. Gene sequencing revealed that both patients had a homozygous mutation in the Gli1 gene (rs2228226 G>C). In conclusion, we suggest that the Gli1 gene (rs2228226 G>C) may be involved in the etiology of SC.

Keywords: bone tumor of mandibular condyle; cone-beam computed tomography; magnetic resonance spectroscopy; synovial chondromatosis; temporomandibular joint; trismus; zinc finger protein GLI1.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chondromatosis, Synovial* / diagnostic imaging
  • Chondromatosis, Synovial* / genetics
  • Chondromatosis, Synovial* / surgery
  • Female
  • Humans
  • Joint Loose Bodies* / complications
  • Joint Loose Bodies* / surgery
  • Magnetic Resonance Imaging
  • Mutation
  • Temporomandibular Joint
  • Zinc Finger Protein GLI1* / genetics

Substances

  • GLI1 protein, human
  • Zinc Finger Protein GLI1