While many cancers are difficult to detect, symptoms of Ewing sarcoma can be recognizable. This rare disease affects the soft tissue surrounding the bones and can spread to the lungs, bone marrow, and even to the liver. Children and young adults are most often affected by this disease. Males are more likely to develop the condition than females. The primary affected areas are the arms, legs, and pelvis. There are no specific symptoms, making it difficult to diagnose.
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If you suspect that you may have the disease, there are a variety of symptoms that you should be aware of. First of all, you should be aware of the fact that 87% of this type of cancer occurs in the bone. While most Ewing sarcoma cases are located in the skeleton, it can also occur in soft tissue around the bones. In addition, a soft tissue tumor can affect the muscles or tendons of the arms and legs. A pPNET tumor is another type of Ewing sarcoma.
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A biopsy of the tumor may be necessary to diagnose Ewing sarcoma. A biopsy of the tumor tissue is important for determining its cause and prognosis. Blood tests may be necessary for diagnosis. If a biopsy is negative, further testing is required to identify the disease. The doctor will perform other procedures to determine whether it is a symptom of the disease. If the tumor is located in the bones, a bone marrow aspiration/biopsy may be needed.
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Ewing sarcoma symptoms are systemic and can resemble flu or an illness. A fever may be present for hours or even days, but if it persists longer than a common cold, it may be Ewing sarcoma. Other symptoms include a painful, lump or swelling in the affected area. While this type of cancer is not painful, it is often not visible until it has grown to a large size.
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Treatment for Ewing sarcoma includes chemotherapy and surgery. In most cases, patients with this cancer will live at least five years after diagnosis. Some people will need treatment for years, but if they have regular check-ups, they may be cured within a year or two. In some cases, the cancer may come back, and amputation is necessary to remove the tumor completely. However, some people will require additional treatments for many years.
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Early detection is vital to the treatment of Ewing sarcoma. The early stage of the disease is the best time for treatment. Surgical resection is one of the main treatments for the disease. It may be necessary to remove the affected bone. The cancer will not respond to the treatment, but it will be treated. If detected early, the disease will respond better to the treatments. A good prognosis is essential for the survival of your child.
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Although symptoms may vary from person to person, they usually involve a warm lump near the surface of the skin, fever, and weakness in the affected area. These symptoms may be due to the growing tumor or the weakening of the bone. If the symptoms persist, it may be a sign that something is wrong. During this time, a physician should be able to determine if the disease is spread to other parts of the body or whether it is recurrent.
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Patients who are diagnosed with Ewing sarcoma should consult their physician as soon as possible. Surgical procedures can help diagnose the disease and may also lead to the treatment of underlying conditions. Most cancer patients undergo radiation therapy and chemotherapy during their treatment. If no treatment is found, the disease will return after a few months. In the meantime, the patient should continue to monitor the signs and symptoms of Ewing sarcoma.
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There are several ways to detect Ewing sarcoma. The symptoms of this disease are systemic and may be confused with other illnesses. The doctor will perform X-rays and other diagnostic tests to confirm the diagnosis. Among the most common tests used to diagnose Ewing sarcoma are MRI and PET scans. These tests may also include blood and urine samples. Some patients may not show symptoms at all or have few symptoms.
