The short answer
The two main bone cancers in children and teens are osteosarcoma and Ewing sarcoma. Both often cause bone pain and swelling, frequently near the knee or in the long bones. Treatment usually combines chemotherapy with surgery, and sometimes radiation for Ewing sarcoma.
The two main childhood bone cancers are osteosarcoma and Ewing sarcoma.
They most often affect older children and teenagers.
Common symptoms are bone pain and swelling, often near the knee or in the long bones.
Osteosarcoma usually starts in the bone itself; Ewing sarcoma can start in bone or nearby soft tissue.
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The simple version
Bone cancer in children is rare. The two most common types are osteosarcoma and Ewing sarcoma. Osteosarcoma usually starts in a long bone, often near the knee. Ewing sarcoma can start in many bones or in the soft tissue around a bone. Both are usually treated with chemotherapy plus surgery, radiation or both.
Who gets it
Osteosarcoma mostly affects teens and young adults. About 440 people age 19 and younger are diagnosed with it each year in the United States. More than half the time, it starts in a long bone near the knee. Ewing sarcoma also mostly affects teens and young adults, from the teen years into the mid-20s. It can start in a bone. It can also start in the soft tissue around a bone.
Signs to watch for
The most common signs are pain and swelling in a bone or joint. These signs may come and go at first. A limp, stiffness, or a fracture with no clear injury can also be a sign. Some children with Ewing sarcoma also get fever, fatigue, or weight loss they cannot explain. Any bone pain that keeps coming back is worth a doctor visit, especially in a growing child.
How doctors diagnose it
Doctors start with imaging tests. An X-ray comes first. A CT scan or MRI usually follows, to see the tumor in more detail. A biopsy is the step that confirms cancer. A small piece of the tumor is removed and checked under a microscope. This step matters a lot. The biopsy should be done by a surgeon who is an expert in bone cancer. It is best if that surgeon also removes the tumor later. A poorly placed biopsy can make that later surgery harder.
How osteosarcoma is treated
Treatment usually starts with chemotherapy. Doctors give it before surgery, to shrink the tumor and kill cancer cells that imaging cannot see. Surgery follows, to remove the tumor completely. Many children can have limb-sparing surgery. This removes the cancer while keeping the arm or leg. Some children need amputation instead. That choice depends on the tumor's size and exact location. Studies show survival is the same whether the first surgery saves the limb or is an amputation. After surgery, children usually get more chemotherapy, to kill any cancer cells left behind.
How Ewing sarcoma is treated
Ewing sarcoma is also treated with chemotherapy first. This usually lasts several months, to shrink the tumor. Then comes local treatment: surgery, radiation, or sometimes both. The choice depends on where the tumor is, and how it responded to chemotherapy. More chemotherapy usually follows. The whole process can take six months to a year. If Ewing sarcoma comes back after treatment, doctors may use high-dose chemotherapy with a stem cell transplant.
Clinical trials
Clinical trials are an option for children with osteosarcoma or Ewing sarcoma. Ask your child's team whether a trial is open for their specific cancer.
Life after treatment
Recovery does not stop when treatment ends. Children who had surgery may need help from a rehabilitation specialist. Treatment can also cause late effects years later, such as fertility problems or a second cancer. Ask your child's team for a written survivorship plan that covers rehab and long-term checkups.
When to call the doctor right away
Treat a fever during chemotherapy as an emergency, not a message to leave. Phone the oncology team at once, day or night, if your child's temperature reaches 100.4°F (38°C) or higher or if they get shaking chills. Chemotherapy lowers blood counts, and CDC says a fever during chemotherapy is a medical emergency, and an infection during chemotherapy can be life-threatening. If you cannot reach the team in minutes, take your child to an emergency department and tell the staff straight away that they are on chemotherapy. Call 911 if breathing becomes hard.
Call the care team right away for sudden severe pain in the affected limb, or a bone that gives way or breaks after only a small knock.
What to ask your child's team
- Is limb-sparing surgery possible? What will recovery and rehab look like?
- How many rounds of chemotherapy are planned, and what side effects should we expect?
- Is a clinical trial available?
- What will follow-up scans and appointments look like once treatment ends?
Bone cancers can come back, and regular monitoring catches this early.
Sources

Common questions
What are the main bone cancers in children?
The two main types are osteosarcoma and Ewing sarcoma. Both most often affect older children and teenagers.
What are the symptoms?
The most common symptoms are bone pain and swelling, often near the knee or in the long bones of the arms and legs.
How are osteosarcoma and Ewing sarcoma different?
Osteosarcoma usually starts in the bone itself, most often near the ends of long bones. Ewing sarcoma can start in a bone or in the soft tissue around it.
How are they treated?
Treatment usually combines chemotherapy with surgery to remove the tumor. Radiation therapy is sometimes used for Ewing sarcoma. Limb-sparing surgery is often possible.
What is limb-sparing surgery?
It is surgery that removes the tumor while saving the arm or leg, often using a bone graft or an implant to replace the removed bone.
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Last updated: 2026-09-29Next planned review: 2027-07-07
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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes, and this is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.
Editorial status: Source checked — This page was written with AI assistance and then compared with the sources listed on it, looking for statements those sources do not back up. That check is not a sentence-by-sentence record and can miss errors. It is not a medical review, and it does not confirm the page is complete or right for your situation.
Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.
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