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Renal angiosarcoma.

D Terris, L Plaine, A Steinfeld

    American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
    |August 1, 1986
    PubMed
    Summary
    This summary is machine-generated.

    Renal angiosarcoma, a rare vascular tumor, is typically managed with surgery. This case shows that radiation therapy can effectively control localized disease and palliate bone metastases in patients with angiosarcoma.

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    Area of Science:

    • Oncology
    • Surgical Pathology
    • Radiation Oncology

    Background:

    • Renal angiosarcoma is a rare vascular malignancy.
    • Surgical resection (nephrectomy) is the primary treatment modality.
    • Adherence of tumor to adjacent structures can complicate surgery.

    Observation:

    • A patient with renal angiosarcoma underwent nephrectomy with tumor adherent to the diaphragm and renal artery.
    • Postoperative radiation therapy was administered to the renal fossa.
    • The patient developed bone and liver metastases but had controlled local disease.

    Findings:

    • Radiation therapy appeared to control the renal fossa disease despite distant metastases.
    • Radiotherapy effectively palliated symptomatic bone lesions.

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  • The findings support the radiosensitivity of angiosarcoma.

    • Implications:

    • Radiation therapy may play a role in managing localized renal angiosarcoma, especially when surgical margins are unclear.
    • Radiotherapy can be crucial for palliation of metastatic bone disease in angiosarcoma.
    • Further research into multimodal treatment strategies for angiosarcoma is warranted.