Ewing sarcoma is a bone cancer. This cancer is serious, but the prognosis has been greatly improved thanks to treatment advances in chemotherapy and radiotherapy.
-Ewing’s sarcoma: a primary bone cancer
-Bone cancer: what are the symptoms of Ewing’s sarcoma?
-Ewing sarcoma: sometimes surgery, chemotherapy and radiotherapy but otherwise
Ewing’s sarcoma: a primary bone cancer
Ewing sarcoma is one of the primary tumors of bone, that is to say that cancer cells originate from bone, and that are not met static cancer located elsewhere in another organ. Ewing sarcoma is unique in touch more often men than women. It also develops mainly in children between 10 and 15 years , more rarely in young adults up to age 25. Cancer cells usually reach the long bones like the femur and tibia. Thus Ewing sarcoma most often for the arms and legs, even though this cancer can affect any bone.
Bone cancer: what are the symptoms of Ewing’s sarcoma?
The symptoms are typically those of bone cancer: bone cancer is painful and swollen. Moreover, it is fragile and may break at the slightest shock. When the tumors grew, they can sometimes go up to affect the bone throughout its length. The diagnosis of Ewing’s sarcoma is based on the radiograph but also require a confirmatory biopsy. It depletes cells in the suspicious area for examination and to determine precisely the nature of cancer. The biopsy is facilitated by examination, CT and MRI, which permanent finely locate tumors. These imaging tests also help in the diagnosis by stating the precise size of the tumors.
Ewing sarcoma: sometimes surgery, chemotherapy and radiotherapy but otherwise
A surgical procedure with removal of regional cancer is sometimes necessary. Otherwise, it now uses to chemotherapy and radiotherapy. These techniques have greatly improved the prognosis of Ewing’s sarcoma. The cure rate is currently 60%.