Ewing sarcoma is a type of cancer that starts in the cells of the bones and the soft tissues surrounding them. It's most common in children and young adults, but can affect people of any age.
This cancer usually starts in the bones of the legs or pelvis, but it can develop in any bone in the body. Sometimes, it begins in the soft tissues of the chest, abdomen, arms, or other areas.
Significant improvements in how Ewing sarcoma is treated have led to better outcomes. More young people diagnosed with this cancer are surviving longer. However, the powerful treatments used can sometimes cause long-term side effects. Doctors often recommend ongoing checkups to watch for these after-effects.
Ewing sarcoma is a type of cancer that usually begins in the bones, often near the legs or pelvis. When the cancer is in the bones, common signs include:
Sometimes, Ewing sarcoma causes symptoms that aren't directly related to the bone. These more general symptoms can include:
If you or your child are experiencing any of these signs and symptoms that are lasting or worrying, make an appointment with a doctor right away. Early diagnosis is important for effective treatment.
If you or your child are experiencing ongoing health concerns that are troubling you, please schedule an appointment with a doctor or other healthcare provider.
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Ewing sarcoma, a type of cancer, has an unclear cause.
Cancer happens when the instructions in a cell's DNA become flawed. Think of DNA as a cell's instruction manual. Normal DNA tells cells to grow and divide at a specific pace, and to die at a specific time.
But in cancer cells, the DNA instructions are messed up. These faulty instructions tell cancer cells to grow and multiply rapidly, ignoring the normal signals to stop growing or die. This is why cancer cells live much longer than healthy cells.
These rapidly dividing cancer cells can form a lump called a tumor. The tumor can grow bigger and push into and damage healthy tissues. Cancer cells can also break off from the tumor and travel to other parts of the body. This spread of cancer is called metastasis.
In Ewing sarcoma, the DNA changes usually affect a gene called EWSR1. Doctors might test the cancer cells to see if this gene is altered if they suspect Ewing sarcoma. If the test shows changes in this gene, it can help confirm the diagnosis.
Ewing sarcoma is a type of cancer that mostly affects children and young adults. While it can occur at any age, it's more frequently seen in this age group. Another factor that seems to increase the risk is having European ancestry. This cancer is less common in people of African or East Asian descent.
Unfortunately, there's no known way to prevent Ewing sarcoma.
Ewing sarcoma, a type of cancer, can sometimes spread from its original location to other parts of the body. This often happens in the lungs and other bones.
Treating Ewing sarcoma usually involves strong medicines and therapies. These powerful treatments can have significant side effects, both immediately during treatment and later on. For example, some common side effects might include nausea, fatigue, or hair loss. Your medical team can help you manage these side effects as they arise. They can also discuss potential long-term side effects that might develop after treatment, and how to watch for them.
Diagnosing Ewing sarcoma often starts with a physical check-up by a doctor. Based on what they find, more tests might be needed.
These tests create pictures of the inside of your body to help pinpoint where the cancer is and how big it is. These imaging tests can include:
A biopsy is a crucial step in confirming the diagnosis. A biopsy involves taking a small piece of tissue from the suspected tumor. This tissue sample is then sent to a lab for testing. There are different ways to do a biopsy:
The lab analyzes the tissue sample to see if it's cancerous. Further tests look at the characteristics of the cancer cells.
A biopsy is essential to confirm the diagnosis of Ewing sarcoma. The results from the biopsy and other tests help the medical team create a personalized treatment plan.
Crucially, the lab tests the cancer cells to find specific changes in their DNA. Ewing sarcoma cells often have changes in a gene called EWSR1. In many cases, the EWSR1 gene joins with another gene called FLI1, creating a new gene called EWS-FLI1. Knowing if these gene changes are present helps doctors confirm the diagnosis and understand the specific type of Ewing sarcoma.
Ewing sarcoma is treated mainly with chemotherapy, surgery, and sometimes radiation therapy or targeted therapy. The best order for these treatments depends on the specific situation.
Chemotherapy: This uses strong medicines to fight cancer. It's often used as the first treatment for Ewing sarcoma, as the medicines can shrink the tumor. This makes it easier for surgeons to remove the cancer or for radiation therapy to target it more effectively. Even after surgery or radiation, chemotherapy may be used to kill any remaining cancer cells. For advanced Ewing sarcoma that has spread, chemotherapy can help ease pain and slow the cancer's growth.
Surgery: The goal of surgery is to remove all the cancer. This might involve taking out a small part of the bone and surrounding tissue. In some rare cases, it might be necessary to remove the entire affected limb (like an arm or leg). Surgeons carefully plan the surgery to minimize the risk of harming healthy tissue and to preserve function as much as possible. Whether a surgeon can remove the cancer without removing the limb depends on things like the size and location of the cancer, and whether chemotherapy has helped shrink it.
Radiation Therapy: This treatment uses powerful energy beams, like X-rays or protons, to target cancer cells. A machine directs the beams to precise spots on the body. Radiation therapy might be used after surgery to kill any remaining cancer cells. It might be the preferred treatment option if surgery isn't possible or if it could harm nearby healthy organs, like the bowel or bladder. Radiation therapy can help slow the growth of advanced Ewing sarcoma and relieve pain.
Targeted Therapy: This type of treatment uses medicines that attack specific ways cancer cells grow. By blocking these specific processes, targeted therapies can cause cancer cells to die. Researchers are exploring targeted therapy for Ewing sarcoma, especially in cases where the cancer returns or doesn't respond to other treatments.
Clinical Trials: Clinical trials study new cancer treatments. These trials give people the chance to try the latest treatments, but the potential side effects may not be fully understood. It's important to talk to your healthcare team about the possibility of joining a clinical trial.
Coping with Ewing Sarcoma: A Ewing sarcoma diagnosis can be overwhelming. It's important to seek support from loved ones, friends, and healthcare professionals. Talk to your doctor about ways to cope with the stress and uncertainty. If you have a child with Ewing sarcoma, your healthcare team can guide you in talking to your child about the cancer in a way they can understand. Maintaining strong relationships with family and friends is crucial. They can provide emotional support and practical help. Consider talking to a counselor, social worker, psychologist, or other mental health professional. Many cancer organizations, like the American Cancer Society, offer support services as well.
Important Note: This information is for general knowledge and should not be considered medical advice. Always consult with your healthcare provider for personalized guidance and treatment options.
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