A 20 -year -old student practiced implementing the clutch to learn to drive that he felt that shooting in his left leg was due to shooting pain and overwork of muscles in the knee. However, when he was diagnosed with a rare tumor due to bone cancer, Emmi was shocked. According to Emmi, an English student at Bristol University – she was suffering from pain and discomfort shortly after starting her driving lesson, which continued to grow slowly.

Initially, Imi and her parents called it “clutch leg” – common discomfort using clutch pedal. He started to reduce the pain and started coming again in the episode. And so, when it once became too much to bear, Imi went to emergency services, where she was injected with painkillers.

Later, she also tried to take physiotherapy for her position, which did not work, inspired her to receive an MRI scan, with the shocking truth – 10 -cm -length tumor – a grape size, in her femur. The doctors then diagnosed her Ewing Sarcoma – a rare and aggressive bone cancer. Then he immediately started a fierce diet of 14 rounds of chemotherapy every two weeks, which reduced the tumor significantly.

Later, Imi underwent surgery for a hip for a hip and femur replacement. Now regular physiotherapy, Imi is cancer-free and has returned to her studies.

What is Ending Sarcoma?

Ewing Sarcoma is a type of bone or soft tissue cancer that occurs mainly in children and young adults. Often found in long bones in the body, symptoms include pain, inflammation and fever.

While ewing sarcoma can develop anywhere, in any bone, doctors say that it is often found in hip bones, ribs, or long bones such as fees, tibia (shinbone), or haumaras (upper arm). It also includes muscles and soft tissues around the tumor. Eving Sarcoma cells can also spread to other areas of the body, including bone marrow, lungs, kidneys, heart, adrenal glands and other soft tissues.

Ewing Sarcoma to Dr. James Ewing gets his name, Dr. Hu first described the tumor in the 1920s.

What is the reason for Ewing Sarcoma?

According to experts, even though the exact cause of the Ewing Sarcoma is not fully understood, studies have discovered chromosomal changes in a cell’s DNA that can lead to the formation of this rare cancer. These changes have not been inherited, but after being born in children, they develop without any clear reason.

In most cases, changes include fusing of genetic material between chromosome 11 and 22. When a certain piece of chromosome 11 is placed next to the EWS gene on chromosome 22, the EWS gene “switch on”. This activation leads to overgrowth of cells and eventually the development of cancer.

Symptoms and symptoms of ewing sarcoma

Patients with ending sarcoma may experience symptoms:

• Pain around the tumor’s site
• Tumor
• Fever
• Weight loss and loss of appetite
• Fatigue and fatigue
• Paralysis
• Tumor

While the symptoms of ewing sarcoma may be attained by other medical conditions or problems. Always consult your doctor for diagnosis.

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