Childhood Cancer
Chapter 2: Bone Sarcomas
BONE SARCOMAS ARE a group of several different cancerous tumors of the bone. The most common bone sarcomas diagnosed in children and adolescents are osteosarcoma and Ewing sarcoma.
This chapter first explains the structure and function of the skeletal system. It then describes osteosarcoma and the four diagnoses known as the Ewing sarcoma family of tumors (ESFT)—Ewing sarcoma of the bone, extraosseous Ewing sarcoma, Askin’s tumor, and peripheral primitive neuroectodermal tumor (PPNET). The sections on each type of bone sarcoma include information about signs and symptoms, how it is diagnosed, and how it is treated.
Table of Contents
All Guides- Introduction
- 1. Diagnosis
- 2. Bone Sarcomas
- 3. Liver Cancers
- 4. Neuroblastoma
- 5. Retinoblastoma
- 6. Soft Tissue Sarcomas
- 7. Kidney Tumors
- 8. Telling Your Child and Others
- 9. Choosing a Treatment
- 10. Coping with Procedures
- 11. Forming a Partnership with the Medical Team
- 12. Hospitalization
- 13. Venous Catheters
- 14. Surgery
- 15. Chemotherapy
- 16. Common Side Effects of Treatment
- 17. Radiation Therapy
- 18. Stem Cell Transplantation
- 19. Siblings
- 20. Family and Friends
- 21. Communication and Behavior
- 22. School
- 23. Sources of Support
- 24. Nutrition
- 25. Medical and Financial Record-keeping
- 26. End of Treatment and Beyond
- 27. Recurrence
- 28. Death and Bereavement
- Appendix A. Blood Tests and What They Mean
- Appendix B. Resource Organizations
- Appendix C. Books, Websites, and Support Groups