Benign, developmental disorder of bone that causes normal skeletal tissue to be replaced by fibrous tissue
Aetiology
- Usually occurs in adolescence
Pathophysiology
- Genetic mutation results in lesions of fibrous tissue and immature bone
- Can affect one bone (monostotic) or more than one bone (polyostotic)
- Defective mineralisation may result in angular deformities and the affected bone is wider with thinned cortices
Clinical presentation
- Bone pain and deformities
Investigations
- Bone scan - show intense increase in uptake during development but the lesion usually becomes inactive
- Extensive involvement of the proximal femur can produce a 'shepherd’s crook' deformity on x-ray
Management
- Bisphosphonates may reduce pain
- Pathological fractures should be stabilized with internal fixation and cortical bone grafts used to improve strength
- Simple intralesional excision alone has a very high recurrence rate