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[Malignant synovialoma (author's transl)].

E Schnepper, G Thiede, P Aschmoneit

    Der Radiologe
    |January 1, 1976
    PubMed
    Summary
    This summary is machine-generated.

    Early diagnosis and treatment of malignant synovialoma are crucial for improving patient outcomes. Radical surgery combined with intensive irradiation can achieve a 5-year survival rate of 30-50%.

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    Area of Science:

    • Orthopedic Oncology
    • Surgical Pathology

    Background:

    • Malignant synovialoma is a rare soft tissue sarcoma.
    • Early recurrence and metastasis significantly impact prognosis.

    Purpose of the Study:

    • To discuss clinical and roentgenographic findings.
    • To outline differential diagnosis, therapy, and prognosis.
    • To evaluate treatment outcomes for malignant synovialoma.

    Main Methods:

    • Literature review of 351 cases.
    • Analysis of 12 own observations.
    • Clinical and roentgenographic assessment.

    Main Results:

    • Early diagnosis is critical for effective treatment.
    • Radical surgery followed by intensive irradiation of the tumor site and draining lymphatics is the recommended therapeutic approach.

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  • A 5-year survival rate of 30-50% is achievable with this combined treatment strategy.

    • Conclusions:

    • Prompt diagnosis and aggressive multimodal therapy are essential for managing malignant synovialoma.
    • Surgical resection and adjuvant radiotherapy improve survival rates.
    • Further research into optimizing treatment protocols is warranted.