Kaposi's Sarcoma
Background
- Angioproliferative disorder caused by HHV-8
- Divided into four types based on clinical circumstance
- Classic - typically presents in middle or old age
- Endemic - endemic in sub-Saharan Africa
- Iatrogenic - associated with immunosuppressive therapy
- AIDS-associated
Clinical Features
- Skin Lesions
- Purplish, reddish blue, or brown macules, plaques, and nodules on the skin
- Ranging from very small to several cm in diameter
- May rapidly evolve and disseminate or remain unchanged over time
- Extracutaneous Manifestations
- Involvement of the mouth and GI tract
- Often asymptomatic but may cause bleeding or diarrhea
- Chronic, indolent course rarely influencing survival
Differential Diagnosis
- Peripheral vascular disease
- Bacillary angiomatosis
- Angiosarcoma
- Hemangioma
Diagnosis
- Biopsy is required for definitive diagnosis
- PCR of skin sample for HHV-8
Management
- Primary goals of treatment: palliation, alleviating lymphedema, improving function, decreasing the size of cutaneous or visceral lesions, and delaying or preventing disease progression
- Surgery may be considered for singular lesions
- Radiation is effective though controversial
- Cryotherapy for local control, though effect is largely cosmetic
Disposition
- Follow up for outpatient treatment
See Also
External Links
References
<UpToDate>
