Osteoid Osteoma
Also known as: Osteoid Osteoma of Bone
Osteoid osteoma is a benign, osteoblastic bone tumour made of a small central nidus (under 1.5 to 2 cm) of vascular osteoid and woven bone, surrounded by reactive sclerosis. It causes characteristic night pain that is relieved promptly by aspirin or other NSAIDs.
It accounts for about 10% of benign bone tumours and 3% of all primary bone tumours. It peaks between 5 and 25 years of age, and is 2 to 3 times more common in males. About half arise in the femur and tibia (the proximal femur, neck and intertrochanteric region, is the commonest site), 10% in the spine (posterior elements, often the lumbar spine), and the remainder in the hands, feet, humerus and talus.
Lesions are described by position: cortical (most common, with dense fusiform sclerosis), cancellous or medullary (little sclerosis, often intra-articular), and subperiosteal (often in the neck of the talus or femur). Intra-articular and spinal lesions are more often missed.
Complications:
- chronic synovitis with effusion and joint contracture
- limb length discrepancy or angular deformity in a growing child
- painful scoliosis (the nidus lies on the concave side of the curve)
- muscle atrophy
- recurrence after incomplete removal
Malignant change does not occur.
Pathophysiology.
The nidus contains high concentrations of prostaglandin E2, with strong expression of cyclo oxygenase 1 and 2, and a dense network of unmyelinated nerve fibres. Prostaglandins explain the pain and the dramatic response to NSAIDs, and the vasodilation they produce drives the surrounding sclerosis and marrow oedema. Rearrangements of the FOS gene are found in most cases.
The natural history is slow spontaneous resolution of the nidus over 3 to 7 years in many patients, which is why prolonged NSAID treatment is an accepted alternative to ablation.













