Jaffe-Campanacci syndrome

Jaffe-Campanacci-Syndrome,

boy 7 Y, tibial bowing and cortical/subcortial mixed sclerosis

Osteofibrous

dysplasia-like adamantinoma treated via intercalary segmental resection with partial cortex preservation using pedicled vascularized fibula graft: a case report. The X-ray, CT image, and MR images of the tumor. a Anteroposterior radiograph. b Lateral radiograph. c Axial CT image. d T1-weighted magnetic resonance sagittal image. e T2-weighted magnetic resonance sagittal image

Osteofibrous

dysplasia-like adamantinoma treated via intercalary segmental resection with partial cortex preservation using pedicled vascularized fibula graft: a case report. The mass was a heterogeneously hypointense and isointense on a T1-weighted magnetic resonance image and b heterogeneously hyperintense on short TI inversion recovery magnetic resonance image. No pathological fracture was confirmed

Osteofibrous

dysplasia • Osteofibrous dysplasia of the tibia - Ganzer Fall bei Radiopaedia

Osteofibrous

dysplasia • Osteofibrous dysplasia of the tibia - Ganzer Fall bei Radiopaedia

Osteofibrous

dysplasia • Osteofibrous dysplasia - tibia - Ganzer Fall bei Radiopaedia

Osteofibrous

dysplasia • Osteofibrous dysplasia - Ganzer Fall bei Radiopaedia

Osteofibrous

dysplasia • Osteofibrous dysplasia - Ganzer Fall bei Radiopaedia

Teenager with

neurofibromatosis type I and knee pain. AP and lateral radiographs of the knee show multiple lucent lesions with thin sclerotic margins in the metaphysis of the femur, tibia and fibula.The diagnosis was multiple non ossifying fibromas in Jaffe Campanacci Syndrome in a patient with neurofibromatosis type I.