- AKA Osteogenic Sarcoma
Definition
- Primary malignant bone-producing bone tumour characterised by production of osteoid
- ie bone matrix produced by malignant cells
Epidemiology
- Second most common malignant neoplasm of bone after multiple myeloma
- 20% of all malignant neoplasms of bone
- Bimodal peak
- Teens
- Elderly
- M:F – 1.5:1
Classification
Anatomical Classification
| Type | Subtypes |
|---|---|
| 1. Central | Further subclassified by grade (high grade, 10-20yo, most common, or low grade) and pathology (conventional, telangiectatic, small cell, giant cell) |
| 2. Juxtacortical (surface osteosarcoma) | Low grade (30-40yo, usually low grade) or high grade Parosteal or Periosteal |
| 3. Intra-cortical | |
| 4. Soft tissue | |
| 5. Secondary |
Aetiology
- Strong genetic influence
- Increased risk in children with familial retinoblastoma (500x)
- RB 1 gene on chromosome 13
- P53 on 17p
- Also associated with chromosomal abnormalities such as
- Rothmund-Thompson syndrome
- Bloom syndrome
Reviewed by Professor Phong Tran, Head of Orthopaedic Surgery, Western Health. Last updated 10 October 2026.