Ewing’s sarcoma refers to a cancer of the bones or soft tissues. In the title, sarcoma is a generic term for cancer of your muscle, tendon, cartilage, nerve, blood vessels and other parts, while Ewing refers to the person who first described the disease in 1921, whose name is James Ewing. Typically, Ewing’s sarcoma happens in the pelvis and the large long bones of the arms and leg, but it can actually occur to any bones in the body. In the treatment process of Ewing’s sarcoma, intense radiation and chemotherapy are often used. So, in order to prevent potential side effects, people who go through the treatment process usually need to be monitored their entire life.
In the united states, Ewing’s sarcoma can be found 1 case per 1 million people every year. About 200 children and young adults in America are affected by Ewing’s sarcoma. Among the affected, most people are under 20 years old. Although Ewing’s sarcoma is more commonly seen in teenagers, it, in fact, can happen at any age. Moreover, men are slightly more likely to be affected by the condition than women. Overall, Ewing’s sarcoma is more commonly seen in white people and African Americans or Asian Americans.
Researchers have found that in the cells of Ewing’s sarcomas, 95% of them have a specific chromosomal translocation, which is a type of genetic mutation. At present, the researches on Ewing’s sarcoma are still ongoing and the exact cause of this translocation remains to be a problem to solve. Also, based on current studies, Ewing’s sarcoma does not appear to be inherited.
Common signs and symptoms of Ewing’s sarcoma may include:
Ewing’s sarcoma is a rare disease and it is often misdiagnosed at first.
To confirm a diagnosis, the doctor often needs to order imaging tests such as X-ray, MR (magnetic resonance) scan, CT (computed tomography) scan, PET (positron emission tomography) scan, and bone scan. Detailed images can help the doctor to see the situation in a clearer way. Also, a biopsy may also be done so that a diagnosis can be confirmed.
Chemotherapy, radiation therapy and surgery are available options for treating Ewing’s sarcoma. These treatment methods can be used alone or in combination.
Based on the size, location of the tumor, whether
the cancer cells have spread to other parts and the patient’s overall health,
the doctor will tailor treatment plans for each individual.
For different patients at different
stages, the doctor may give a different
prognosis. Usually, if the cancer cells have not spread to other parts of the
body, up to 80% of the patients with Ewing’s sarcoma can be cured. However, if
the tumor has spread, then the survival
rate would be much lower.
The treatment and recovery of Ewing’s
sarcoma are pretty difficult because the
tumor can spread from its original site to other parts of the body such as bone
marrow, nearby bones and even the lungs. That’s why even if patients with
Ewing’s sarcoma become better after one treatment process, they may need to
return to the hospital again because the condition has returned. Also, the side
effects of radiation therapy can be
substantial.
Keywords: Ewing’s sarcoma.
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