Mayo Clinic doctors have significant expertise and experience in treating patients with Ewing's sarcoma. Medical care is enhanced by research and the availability of the latest technology. The National Cancer Institute has designated Mayo Clinic Cancer Center as a comprehensive cancer center in recognition of its superior depth and breadth of capabilities. The multidisciplinary team of experts who provide medical care for Ewing's sarcoma patients includes pediatric oncologists, medical oncologists, orthopedic oncologists (orthopedic surgeons who specialize in bone and soft tissue tumors), pediatric surgeons, radiation oncologists, plastic surgeons, vascular surgeons and rehabilitation experts.
An X-ray, ultrasound, computed tomography (CT) scan, positron emission tomography (PET) scan or magnetic resonance imaging (MRI) may be used to evaluate suspected cases of Ewing's sarcoma. A specialist must biopsy a mass when Ewing's sarcoma is suspected. A bone marrow biopsy may also be needed to evaluate the extent the of disease. Read more about diagnosis of Ewing's sarcoma.
Patients with Ewing's sarcoma receive a combination of cancer-fighting drugs (chemotherapy) as well as surgery or radiation. In about 80 percent of Ewing's sarcoma cases involving an arm or leg, the limb can be saved. Mayo Clinic has significant experience in limb-saving techniques, including bone grafts, rotationplasty and prosthetic implants. Patients also may participate in clinical trials for this disease. Read more about treatment for Ewing's sarcoma.
The Ewing's family of tumors includes cancerous tumors affecting soft tissue or bone. This rare disease most often occurs in children or young adults. The most common type of Ewing's tumor, accounting for more than 80 percent of Ewing's cases, grows in or near bones, most commonly the large bones in the leg (femur and tibia) and the upper arm bone (humerus). Ewing's sarcoma may also occur in other bones or tissue.
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