Kaposi's Sarcoma

Revision as of 09:32, 20 January 2016 by Kshigyo (talk | contribs) (Kaposi Sarcoma)
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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

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