It can also spread to other parts of the body and organs.
This article will explore the types of Ewing sarcoma, its symptoms, diagnosis, treatment, and prognosis.
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Types of Ewing Sarcoma
There are two types of Ewing sarcoma.
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Causes
While there is no definitive cause for Ewing sarcoma, some factors may increase its risk.
They are merely things to keep in mind.
It is rare in Black individuals in the United States.
Diagnosis
Many different tests may be used to help diagnose Ewing sarcoma.
A physical exam and complete medical history are conducted.
Other tests performed on the biopsied material may include cytogenetic testing or biomarker testing.
Surgery
In most cases, surgery to remove the tumor will not result in disability.
For arms and legs, limb-sparing surgery keeps the limb intact.
It may use bone grafts or an internal prosthesis (such as a rod).
Amputation is rarely needed.
The overall five-year survival rate for Ewing sarcoma is 63%.
But the prognosis depends on the stage at which the cancer was diagnosed.
Talk with your treatment team about your or your child’s situation and prognosis.
Its important to put to gather a support team.
It is a cancer of the bones or the surrounding soft tissue.
It’s thought to be associated with chromosomal changes but is not hereditary.
There are a variety of treatments for it, including chemotherapy, surgery, and radiation therapy.
This will keep you informed and help you make informed decisions regarding care.
Children’s Hospital of Philadelphia.Ewing sarcoma.
National Cancer Institute.Ewing sarcoma treatment (PDQ) - patient version.
Johns Hopkins Medicine.Ewing sarcoma in adults.
Boston Children’s Hospital.Ewing sarcoma.
Children’s Oncology Group.What is a clinical trial?
American Cancer Society.Surgery for Ewing tumors.
American Cancer Society.Survival rates for Ewing tumors.
