Ewing sarcoma is a cancer that tends to start in the bone. It's named after James Ewing, MD. He first described this sarcoma in 1921. He noticed that the cells of what came to be called Ewing sarcoma looked different under the microscope than the cells of other kinds of bone tumors. Dr. Ewing also found that this type of tumor was more likely to respond to radiation therapy than other bone cancers.
Experts later found this same type of tumor in soft tissues. They called it extraosseous Ewing tumor. (Extraosseous means outside of the bone.) Another very rare childhood cancer that's a lot like these sarcomas is called peripheral primitive neuroectodermal tumor. It can start in the bone or soft tissues.
These tumors are now all referred to as the Ewing family of tumors, Ewing tumors, or Ewing sarcomas. They are all treated in similar ways.
Studies of Ewing tumors have found that they tend to have the same kinds of changes in the chromosomes or DNA inside the tumor cells. These changes are found only in the tumor cells. They're not genetic changes that are passed on in families. This means that a parent's genes did not cause their child to get cancer. Experts don't know why these gene changes happen.