Cancer Types A-Z

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Overview

Ewing sarcoma is a rare and aggressive cancer that forms in the bone or soft tissue, most commonly in children and adolescents. It usually affects the pelvis, femur, ribs, and chest wall.

Symptoms

  • Pain or swelling at the tumor site
  • Fever or fatigue
  • Bone fracture with minor trauma
  • Limping or decreased movement

Causes & Risk Factors

  • Exact cause unknown; associated with a chromosomal translocation (EWSR1-FLI1)
  • Most common in children and teenagers
  • Slight male predominance
  • Not strongly linked to inherited genetic syndromes

Diagnosis

  • X-ray, MRI, or CT of affected area
  • Biopsy with cytogenetic testing
  • Bone scan or PET-CT
  • Bone marrow biopsy (to rule out spread)

Treatment Options

  • Neoadjuvant chemotherapy (initial systemic treatment)
  • Surgical resection (limb-sparing or resection of affected bone)
  • Radiation therapy (if surgery is not feasible or for residual disease)
  • Adjuvant chemotherapy (after local treatment)

Prognosis

  • 5-year survival for localized disease: ~70%
  • Worse prognosis for metastatic or relapsed disease
  • Prognosis improves with good chemotherapy response and complete surgical resection

Living with this Cancer Type

  • Physical rehabilitation and growth support (in young children)
  • Psychosocial support and peer integration
  • Long-term monitoring for late effects of chemotherapy and recurrence

Prevention & Screening

  • No known prevention methods
  • No standard screening; early evaluation of persistent bone pain is key

FAQs

Q: Is Ewing sarcoma a childhood cancer?
A: Yes, most commonly occurs in people under 20 years old.

Q: Can it be cured?
A: Yes, especially if localized and treated aggressively with chemo and surgery.

Q: Does it affect growth?
A: It may, especially if the growth plates are involved or due to treatment effects.

Resources

  • CureSearch for Children’s Cancer
  • American Cancer Society
  • ClinicalTrials.gov
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