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Distal Femoral Non-Epiphyseal Cortical Chondroblastoma Confirmed with H3F3B p. Lys36Met Mutation.

Haiyan GuLingling SunJiufa CuiLan YuJi-Gang Wang
Published in: Fetal and pediatric pathology (2022)
Background: Chondroblastoma is a primary bone tumor typically arising from the intramedullary space of the epiphysis or epimetaphysis. A non-epiphyseal chondroblastoma is uncommon. Case report: An 11-year-old girl presented with an eccentric cortical osteolytic lesion in the distal femur metaphysis. The typical morphology, diffuse H3.3 K36M immunohistochemical expression and H3F3B point mutation ( c. 110A > T ) unequivocally supported the diagnosis of chondroblastoma. Discussion: We described a non-epiphyseal cortical-based chondroblastoma involving the distal femur harboring the typical H3F3B mutation. Non-epiphyseal chondroblastoma may harbor the H3F3B mutation.
Keyphrases
  • bone mineral density
  • case report
  • minimally invasive
  • postmenopausal women
  • tyrosine kinase
  • high grade
  • high intensity
  • bone regeneration