Ewing sarcoma is an aggressive tumor mainly affecting adolescents and young adults, representing about 10-15% of all bone sarcomas.
01 | Introduction
Ewing sarcoma is a form of cancer that develops from cells in bones surrounding soft tissues, primarily affecting children and young adults. While it can occur in any bone, it normally begins in the bones of the legs and pelvis. Ongoing research and development of new treatments have helped many Ewig sarcoma patients to live longer cancer-free.
02 | Symptoms
Parents and caregivers may confuse the symptoms of Ewing sarcoma with sports injuries. A key difference, however, is that Ewing sarcoma symptoms can initially fade and then return or worsen. Common symptoms include:
03 | Diagnosis
The diagnosis of Ewing sarcoma typically starts with a physical exam. Depending on the results of the exam, additional tests and procedures may be required, such as:
04 | Treatments
Determining the treatment for Ewing sarcoma depends on the patient’s situation. Common treatments include chemotherapy, surgery and radiation therapy.
Learn More
For more information on Ewing sarcoma and supportive resources, please visit mayoclinic.org.
References
https://www.mayoclinic.org/diseases-conditions/ewing-sarcoma/symptoms-causes/syc-20351071
https://www.cancer.org/cancer/types/ewing-tumor/about/key-statistics.html
https://www.ncbi.nlm.nih.gov/books/NBK559183/
https://my.clevelandclinic.org/health/diseases/21752-ewings-sarcoma