What is Synovial Sarcoma?
Synovial sarcoma is a rare form of soft tissue cancer that usually develops near the joints of the arms or legs. Despite its name, it doesn’t actually come from synovial tissue but can occur in almost any part of the body, including the lungs or abdomen.
What are the symptoms?
Symptoms vary but often include a lump or swelling that may be painful or tender. Some patients experience stiffness, limited movement, or numbness if the tumor presses on nerves.
How is it diagnosed?
Doctors usually diagnose synovial sarcoma through imaging tests like MRI or CT scans, followed by a biopsy to confirm the presence of cancer cells.
What treatments are available?
Treatment often includes surgery to remove the tumor, sometimes followed by radiation therapy or chemotherapy. Each case is different, so treatment plans are personalized.
Can people live long-term with synovial sarcoma?
Yes—many patients live for years after diagnosis, especially with early detection and proper treatment. Advances in therapy continue to improve survival and quality of life.
Where can I find support?
You’re not alone. At SynovialSarcomaSurvivors.org, patients and caregivers connect to share experiences, ask questions, and find hope from others who truly understand.