Childhood Cancer
Chapter 4: Neuroblastoma
NEUROBLASTOMA IS A CANCER of newly developing cells in the sympathetic nervous system (described below). The average age at diagnosis is around 2 years old. Most children are diagnosed before the age of 5, and diagnosis is rare after age 10. Although neuroblastomas can develop anywhere in the sympathetic nervous system, from the neck to the pelvis, more than half of these cancers originate in an adrenal gland in the abdomen. Symptoms of this disease vary depending on the location of the primary tumor.
First, this chapter looks at the structure and function of the sympathetic nervous system. Then it describes who gets neuroblastoma, what the signs and symptoms are, how it is diagnosed, and how doctors determine the prognosis. The chapter ends with a discussion about the newest treatment options.
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