7 Facts You Need to Know about Childhood Ewing sarcoma
What is Ewing Sarcoma?
Ewing sarcoma is a rare cancer that grows in bones or soft tissues, primarily in children.
Who Gets Ewing Sarcoma?
Ewing sarcoma usually affects children and teens, most commonly between ages 10 and 20.
Common Symptoms
Pain, swelling, or lumps in the arms, legs, chest, or pelvis are common symptoms.
How is it Diagnosed?
Diagnosis involves X-rays, MRIs, CT scans, biopsies, and sometimes PET scans for clarity.
Treatment Options
Ewing sarcoma is treated with chemotherapy, surgery, and sometimes radiation therapy.
Survival Rate
Early detection boosts survival rates, with localized Ewing sarcoma having around 70% survival.
Potential Long-Term Effects
Survivors may face bone growth issues, but can lead active lives post-recovery.
Support and Awareness
Support groups and awareness are essential in the fight against childhood Ewing sarcoma.
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