Chondroblastic Osteosarcoma: Aggressive Bone Cancer in Youth
Chondroblastic osteosarcoma (COS) is a high-grade malignant bone tumor producing cartilage matrix. It comprises ~10–25% of osteosarcomas.
Epidemiology
- Peak incidence: 10–25 years (adolescents/young adults).
- Slight male predominance.
- Common sites: Distal femur, proximal tibia, proximal humerus.
Presentation
- Pain (night, activity-related), swelling, palpable mass.
- Pathologic fracture (10–15%).
- Systemic: Fever, weight loss, fatigue (advanced).
Diagnosis
- X-ray: Mixed lytic/sclerotic lesion, "sunburst" periosteal reaction, Codman's triangle.
- MRI: Marrow/soft tissue extent; skip metastases.
- Chest CT: Pulmonary metastases (most common site).
- Biopsy: Core needle; confirms cartilage-producing malignant cells.
Treatment
- Neoadjuvant chemotherapy: MAP regimen (methotrexate, doxorubicin, cisplatin) ± ifosfamide.
- Wide surgical resection: Limb-salvage (endoprosthesis, allograft) or amputation.
- Adjuvant chemotherapy: Tailored to histologic response (necrosis %).
Prognosis
5-year survival: ~60–70% localized; <30% metastatic. Poor histologic response (<90% necrosis) worsens outlook.
Multidisciplinary sarcoma center care is essential.
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