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Osteoid osteoma in Child
Other Resources UpToDate PubMed

Osteoid osteoma in Child

Contributors: Alexander Chait, Stephanie E. Siegrist MD
Other Resources UpToDate PubMed

Synopsis

Causes / typical injury mechanism: An osteoid osteoma (OO) is a small, benign, bone-forming neoplasm with a characteristic nidus that has no potential for malignant transformation. The distinctive lesion is less than 2 cm in diameter and forms nonprogressive round-to-oval tumors directly on mature bone. 

Classic history and presentation: Patients classically present with localized pain that starts as a mild, intermittent, dull ache that persists and gradually increases in intensity. Pain typically becomes increasingly more severe at night and is relieved with NSAIDs.

The order of frequency of affected sites is the appendicular skeleton (lower extremities such as the femur and tibia are more commonly affected than upper extremities), spine, feet (predilection for the talar neck), and hands (predilection for phalanges).

Prevalence: Five percent of all bone tumors and 11% of benign bone tumors (third most common benign bone tumor); one study calculated the incidence of 0.063 / 1 000 000 per year.

Age: 5-40 years. Most patients are younger than age 20.

Sex / gender: Males are more commonly affected (ranges from a 2:1 to 3:1 male-to-female ratio).

Risk factors: Alterations involving chromosome 22q (contains genes involved in cellular proliferation).

Pathophysiology: The exact pathogenesis is unknown. This lesion is considered a neoplasm derived from osteoblasts with 3 concentric layers:
  • The central osteoid-rich nidus with dilated vessels and woven bone that may appear calcified.
  • A fibrovascular rim that may appear lytic due to resorption by osteoclasts.
  • A sclerotic border from new bone formation.
The nidus is associated with amplified levels of cyclooxygenase-2 expression that leads to increased prostaglandins E2 and I2 (prostacyclin), causing local inflammation and vasodilation. A high prevalence of intralesional unmyelinated nerve fibers result in the characteristic pain that is relieved by NSAIDs.

Grade / classification system: OO is considered a stage-2 ("active") lesion according to the Musculoskeletal Tumor Society's (MSTS) staging system for benign tumors.

The lesions are further classified by location as cortical, cancellous, or subperiosteal, with cortical being the most common.

Related topic: osteoma

Codes

ICD10CM:
D16.9 – Benign neoplasm of bone and articular cartilage, unspecified

SNOMEDCT:
302859004 – Osteoid osteoma

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Diagnostic Pearls

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Differential Diagnosis & Pitfalls

  • Malignant bone tumors (eg, Ewing sarcoma)
  • Other benign bone tumors, eg:
    • Osteoblastoma
    • Chondroblastoma
    • Adamantinoma
    • Metaphyseal fibrous defect
    • Enchondroma
    • Eosinophilic granuloma
  • Bone cysts
  • Brodie abscess
  • Osteomyelitis
  • Inflammatory arthritis
  • Septic arthritis
  • Stress fractures
  • Avascular necrosis of hip
  • Osteofibrous dysplasia
  • Tuberculosis
  • Neuromuscular conditions
  • Avascular necrosis

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      Therapy

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      References

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      Last Reviewed:10/08/2023
      Last Updated:10/22/2023
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      Osteoid osteoma in Child
      A medical illustration showing key findings of Osteoid osteoma
      Copyright © 2024 VisualDx®. All rights reserved.