βš•οΈ

Medical Disclaimer

The information on this page is for educational purposes only and is not intended to replace professional medical advice, diagnosis, or treatment.

Always seek the advice of your doctor or other qualified health professional with any questions you may have regarding a medical condition.

🚨Emergency? If you have severe symptoms, difficulty breathing, or think it's an emergency, call 000 immediately.

Osteoid Osteoma (Benign Bone Tumor Causing Night Pain)

Benign bone tumor (non-cancerous growth) causing severe night pain relieved by aspirin or NSAIDs - small nidus (5-15mm) produces prostaglandins causing characteristic pain pattern, most common in long bones of adolescents and young adults, cured by radiofrequency ablation (95% success) or surgical excision

πŸ“…Last reviewed: January 2025πŸ₯Bones & Joints

πŸ“–What is Osteoid Osteoma (Benign Bone Tumor Causing Night Pain)?

Benign bone tumor (non-cancerous growth) causing severe night pain relieved by aspirin or NSAIDs - small nidus (5-15mm) produces prostaglandins causing characteristic pain pattern, most common in long bones of adolescents and young adults, cured by radiofrequency ablation (95% success) or surgical excision

πŸ”¬What Causes It?

  • UNKNOWN ETIOLOGY - osteoid osteoma is benign bone tumor of unclear cause (not hereditary, not associated with trauma or infection, likely represents abnormal bone formation during growth)
  • NIDUS FORMATION - central tumor 'nidus' (5-15mm core) produces excess PROSTAGLANDINS (inflammatory chemicals causing pain, dilates blood vessels causing hyperemia and night pain)
  • REACTIVE BONE SCLEROSIS - surrounding bone responds to nidus by forming dense reactive sclerotic bone (body trying to wall off tumor, creates characteristic appearance on X-ray)
  • NO MALIGNANT POTENTIAL - osteoid osteoma NEVER transforms to cancer (100% benign, may spontaneously resolve over many years but symptoms typically persist requiring treatment)

⚠️Risk Factors

ℹ️

You may be at higher risk if:

  • AGE 10-30 years - peak incidence in adolescents and young adults (75% occur in second and third decades of life, rare in children under 5 or adults over 40)
  • MALE PREDOMINANCE - males affected 2-3 times more than females (reason unknown)
  • ACTIVE GROWTH PHASE - tumor develops during skeletal growth (likely related to active bone remodeling in adolescence)
  • LONG BONES - femur and tibia most common sites (50-60% occur in lower extremity long bones, 20% spine, 10% upper extremity, 10% foot/ankle)
  • CORTICAL BONE LOCATION - 80% occur in cortex (outer shell of bone) vs medullary cavity (inner marrow space), cortical location causes more reactive sclerosis and pain

πŸ›‘οΈPrevention

  • βœ“CANNOT BE PREVENTED - osteoid osteoma is benign tumor of unknown cause (not related to lifestyle, trauma, or preventable factors)
  • βœ“Early diagnosis and treatment prevent chronic pain and disability (delayed diagnosis common - average 1-2 years from symptom onset to diagnosis due to low awareness)
  • βœ“Recognize classic symptoms (night pain relieved by NSAIDs in young patient) to prompt early imaging and diagnosis
  • βœ“Awareness in athletes with persistent bone pain not responding to usual treatments (may be osteoid osteoma rather than stress fracture or growing pains)