Also known as: Soft tissue tumors, Askin tumor, peripheral primitive neuroectodermal tumor
What is Ewing sarcoma?
Ewing sarcoma is a rare type of cancer that usually develops in the bones or soft tissue around the bones (cartilage/nerves) of children 10-20 years of age. The pelvis, femur, ribs, or shoulders are often where they start.
What causes Ewing sarcoma?
The cause of Ewing sarcoma is not entirely clear. It doesn't appear to run in families but probably occurs following a gene mutation from exposure to harmful environmental factors (chemicals, radiation etc.).
What are the signs and symptoms of Ewing sarcoma?
Pain, fever and swelling for a long time where the tumor presents; bone breaks without a reason, difficulty with bladder control, and tiredness and weight loss may be presenting features.
What are Ewing sarcoma care options?
Treatment for Ewing sarcoma may include surgery, radiation therapy, chemotherapy, targeted therapy or some combination of these treatments.
Nicklaus Children’s Cancer & Blood Disorders Center is participating in a clinical trial of an investigational drug in children with metastatic tumors in the Ewing’s sarcoma family. Request more information about the clinical trial.
This page was last updated on: January 14, 2021 10:36 AM
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Sarcomas are rare kinds of cancers that affect the body’s soft tissues. They are given different names depending on the type of cell or tissue involved including muscles, tendons, bone, fat, etc.
Chemotherapy is a common form of cancer treatment. It refers to drugs that are often used to kill cancer cells and prevent them from coming back.
Radiation therapy is a common form of cancer treatment. It refers to exposing the body to beams of radiation that are used to kill cancer cells and prevent them from coming back.