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[Stewart-Treves syndrome].

C Pirard, A Bourlond

    Dermatologica
    |January 1, 1985
    PubMed
    Summary
    This summary is machine-generated.

    Stewart-Treves syndrome, a rare angiosarcoma, developed 14 years post-mastectomy and radiotherapy for breast cancer. Surgical excision, grafting, and radiotherapy controlled the condition for 20 months, with presented ultrastructural and immunopathological features.

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    Area of Science:

    • Oncology
    • Pathology
    • Dermatology

    Background:

    • Stewart-Treves syndrome is a rare complication of chronic lymphedema.
    • It typically manifests as angiosarcoma in patients with a history of mastectomy and radiotherapy for breast cancer.