Fact-sheet: Osteoid osteoma
Updated on 10/20/2023 at 11:06 AM
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Definition
Common benign tumor:
- 4% of primary bone tumors
- 15% of benign bone tumors
Mainly affects children and young adults (peak frequency between 7 and 25 years).
Slight male predominance (sex ratio 2-3/1).
Typical locations:
- long bones in 70 to 80% of cases (femur and tibia in 60% of cases)
- posterior vertebral arch.
Several types: cortical, intramedullary, subperiosteal, or intra-articular.
Clinical features
Insomnia-causing nocturnal pain relieved by aspirin.
Radiography
Typical cortical form
Nidus = cortical lucency less than 15 mm, with possible central calcification not always visible on plain radiographs.
Reactive cortical thickening secondary to periosteal apposition (except for intra-articular osteoid osteoma).
CT
Same imaging features as on radiographs; CT is useful to identify the nidus if not visible on radiographs.
Typical cortical form
Round shape on axial images and oval on coronal/sagittal images, with a maximum/minimum diameter ratio < 2.5
Well-defined margins
Central calcification
Circumferential radiolucent rim
Peripheral sclerosis with ill-defined margins 1A1
Feeding vessel sign
MRI
Typical cortical form
Nidus: T2 hyperintense, T1 iso- to hypointense.
Cortical thickening hypointense on all sequences.
Intense marrow edema centered on the nidus, falsely worrisome.
Indications: - atypical appearance on radiographs/CT - dynamic sequences are useful to identify the nidus = arterial enhancement with rapid, partial wash-out
Management
Percutaneous treatments: laser photocoagulation, radiofrequency ablation, cryotherapy
Medical treatment: bisphosphonates
Surgical excision: invasive, used when percutaneous treatment is contraindicated (difficult access, proximity to neurovascular structures).
Differential diagnosis
Osteoblastoma: larger, involves the spine and flat bones, with milder adjacent bone sclerosis.
Stress fracture: linear.
Cortical osteitis: poorly defined, laminated osteolysis, soft tissue collection.