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[Synovial sarcoma].

L J Jørgensen, H S Poulsen, A M Nordentoft

    Ugeskrift for Laeger
    |May 22, 1989
    PubMed
    Summary

    Synovial sarcoma, a rare soft tissue tumor, shows poor prognosis with high recurrence rates. Survival rates for operable cases were 42% at five years and 31% at ten years.

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    Glenohumeral movement patterns after puncture of the joint capsule: An experimental study.

    Journal of shoulder and elbow surgery·2012

    Area of Science:

    • Orthopedic Oncology
    • Surgical Pathology

    Context:

    • Synovial sarcoma is a rare soft tissue malignancy.
    • This study reviewed 26 cases diagnosed between 1962 and 1984.
    • Most patients were referred after initial surgery elsewhere.

    Purpose:

    • To analyze the clinical characteristics, treatment outcomes, and survival rates of synovial sarcoma.
    • To evaluate the effectiveness of local excision versus amputation for synovial sarcoma.

    Summary:

    • Twenty-three of 26 synovial sarcoma cases were operable, with 17 undergoing local excision and 6 amputation.
    • Local recurrence occurred in 14 patients within 12 months.
    • Five-year and ten-year survival rates for operable cases were 42% and 31%, respectively.

    Impact:

    • Highlights the aggressive nature of synovial sarcoma and challenges in its management.
    • Underscores the need for specialized centers in treating rare bone and soft tissue tumors.
    • Provides long-term survival data crucial for prognostic assessment and treatment planning.

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