Secondary angiosarcoma

Introduction

Relatively rare malignant tumors derived from the internal lining of blood vessels or lymphatic vessels.

Unlike primary, confined to the skin.
Cutaneous angiosarcoma – a.k.a. Stewart-Treves syndrome.

Epidemiology

Risk factors

Localized radiation therapy – strongest risk factor
Chronic axillary lymphedema, often precipitated by surgical LND

Histopathology

Histopathologically, infiltration of the dermis with slit-like abnormal vascular spaces.

Clinical manifestations

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  • Multiple ecchymoses or purpuric masses on the skin of the breast, axilla, or upper arm
  • 4-8 years following completion of breast cancer therapy.
  • Metastasis
    • As with most sarcomas, early hematologic metastasis is common.

Management

When possible, surgical resection is potentially curative.
Prognosis is poor b/c the tumor is usually widespread by the time of diagnosis.

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