Yahoo Web Search

  1. 9.0/10 (33 reviews)

    cancerresearchuk.org has been visited by 10K+ users in the past month

    Get Information On Surviving Cancer. Cancer Research UK. Learn More About Cancer Today. Cancer Research UK. Together We Are Beating Cancer.

Search results

  1. People also ask

  2. Jun 20, 2024 · Synovial sarcoma is a rare, slow-growing cancer that affects your soft tissues. Symptoms develop over time and may include a noticeable lump, pain or swelling.

  3. How common is synovial sarcoma? Synovial sarcoma accounts for 5% to 10% of soft-tissue tumors. For every one million people, one to two are diagnosed with synovial sarcoma per year in the US.

  4. Aug 23, 2016 · Most synovial sarcoma patients discover their tumor from a lump, and for some, related pain. It’s important to see a doctor if you find a lump or have persistent, unprovoked pain in a soft tissue, such as the muscle of an extremity or from within your abdomen.

    • Devon Carter
  5. May 19, 2021 · Introduction. Synovial sarcoma is a relatively rare malignancy representing a soft tissue sarcoma (STS) of uncertain differentiation. It accounts for 5–10% of all STS [1, 2, 3].

    • Aaron M. Gazendam, Snezana Popovic, Sohaib Munir, Naveen Parasu, David Wilson, Michelle Ghert
    • 10.3390/curroncol28030177
    • 2021
    • Curr Oncol. 2021 Jun; 28(3): 1909-1920.
  6. sarcoma.org.uk › types-of-sarcoma › synovial-sarcomaSynovial sarcoma

    There are an average of 79 cases of synovial sarcoma diagnosed every year in England. Synovial sarcoma makes up 2% of all soft tissue sarcomas, and about 0.03% of all cancers. Although synovial sarcoma can affect anyone of any age, the median age at diagnosis is 42 years old.

  7. Apr 27, 2023 · Synovial sarcoma is a rare type of cancer that tends to occur near large joints, mainly the knees. Synovial sarcoma usually affects young adults. Synovial sarcoma begins as a growth of cells that can multiply quickly and destroy healthy tissue.

  8. Aug 23, 2023 · Synovial sarcoma (SS) is a rare and malignant tumor of the connective tissues that presents challenges in diagnosis and treatment. 1,2 This article describes the epidemiology, clinical and genomic characteristics of SS, and the patient pathway from diagnosis to treatment.

  1. People also search for