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Osteosarcoma is a high-grade malignant bone-forming tumor characterized by production of osteoid by malignant mesenchymal cells.
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| Histological classification | Morphological classification | Etiological classification |
|---|---|---|
| Conventional os. | Parosteal os. | Primary os. |
| Telangiectatic os. | Periosteal os. | Secondary os. |
| Small cell os. | High-grade surface os. |
![Updated classification of human malignant, bone mass-depositing osteosarcoma considering the latest WHO 2020 guidelines for bone tumors. The picture outlines the location of tumors (note that it can be central or in the surface of the bone, or intramedullary in the bone marrow medulla) and associated molecular and clinical features. Compiled from revision of literature from [34,37,38]. MDM2— human homolog of mouse double minute 2; CDK4—cyclin-dependent kinase 4. Created with BioRender.com (figure created on 13 March 2023).
Martins-Neves SR, Sampaio-Ribeiro G, Gomes CMF. Self-Renewal and Pluripotency in Osteosarcoma Stem Cells’ Chemoresistance: Notch, Hedgehog, and Wnt/β-Catenin Interplay with Embryonic Markers. International Journal of Molecular Sciences. 2023; 24(9):8401. https://doi.org/10.3390/ijms24098401](attachment:0f395a94-4892-4166-a4e2-533b9ac888c9:ijms-24-08401-g001.png)
Updated classification of human malignant, bone mass-depositing osteosarcoma considering the latest WHO 2020 guidelines for bone tumors. The picture outlines the location of tumors (note that it can be central or in the surface of the bone, or intramedullary in the bone marrow medulla) and associated molecular and clinical features. Compiled from revision of literature from [34,37,38]. MDM2— human homolog of mouse double minute 2; CDK4—cyclin-dependent kinase 4. Created with BioRender.com (figure created on 13 March 2023).
Martins-Neves SR, Sampaio-Ribeiro G, Gomes CMF. Self-Renewal and Pluripotency in Osteosarcoma Stem Cells’ Chemoresistance: Notch, Hedgehog, and Wnt/β-Catenin Interplay with Embryonic Markers. International Journal of Molecular Sciences. 2023; 24(9):8401. https://doi.org/10.3390/ijms24098401
| Type | Age | Description |
|---|---|---|
| Primary (de novo) | 10-25 years | Most common (75%) |
| Secondary | > 40 years | Post-radiation, Paget’s disease, osteogenesis imperfecta, fibrous dysplasia |
Secondary osteosarcoma:
| Malignant degeneration of benign entities | Germline abnormalities |
|---|---|
| ‣ | ‣ |
| Large bone infarction | ‣ |
| Post-radiotherapy | ‣ |
Epidemiology:
| Feature | Description |
|---|---|
| Incidence | ~20% of all primary bone tumors |
| Age | 10–25 years (primary peak); second smaller peak >40 years (often secondary) |
| Sex | Male > Female (1.5–2:1) |