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KAPOSI SARCOMA
HABAKUK LARRY OMONDI
Introduction
• A multifocal systemic tumor of endothelial
cell origin.
• linked with human herpesvirus 8 infection
• Has Four clinical variants
• Responds to radiation and chemotherapy,
Clinical variants of KS
• classic KS
• endemic African KS
• immunosuppressive therapy–related KS
• HIV/AIDS-related KS
Classic KS
• Occurs in elderly males of eastern
European heritage.
• Predominantly arises on the legs but also
occurs in lymph nodes and abdominal
viscera.
• slow progression and has good prognosis
African-Endemic KS
• bimodal age distribution young adults, mean
age 35; and young children, mean age 3
years
• Males > females
• Has poor prognosis (young adults 5–8 years;
young children 2–3 years)
• Four clinical patterns
African-Endemic KS patterns
a) Nodular type: benign course and resembles classic
KS.
b) Florid or vegetating type: more aggressive. Nodular
extend deeply into the subcutis, muscle, and bone.
c) Infiltrative type: more aggressive has
mucocutaneous and visceral .
d) Lymphadenopathic type: children and young adults.
confined to lymph nodes and viscera, also involves
the skin and mucous membrane.
Iatrogenic Immunosuppression-
Associated KS
• Rare.
• Most commonly in solid-organ transplant
recipients
• chronic use of immunosuppressive drugs
• Resolves on cessation of
immunosuppression.
HIV/AIDS-Associated KS
• AIDS increases risk of KS ( 20,000 times that
those not infected with HIV)
• Common in homosexual men
• Rapid progression, extensive systemic
involvement
• KS of the bowel and/or lungs is responsible
for numerous deaths
Pathogenesis
• Initially polyclonal proliferation is due
angiogenic factors.
• Later becomes monoclonal.
• KS lesions produce growth factors.
• It is not know how HHV8 promotes the
process.
Clinical manifestation
• Mucocutaneous lesions are usually
asymptomatic
• lower extremities - edema and moderate
to severe pain
• Urethral or anal canal lesions-
obstruction
• Pulmonary KS - bronchospasm,
intractable coughing, shortness of breath,
progressive respiratory failure.
Skin lesions
ecchymotic-
like macule
patches
papules,
plaques
nodules tumours
The lesions are normally palpable even at the
patch stage.
Classic ks
African KS
Oral kaposi sacroma
Investigations
• Skin biopsy- Vascular channels lined by
atypical endothelial cells.
- extravasated erythrocytes
with hemosiderin deposition
Imaging – abdominal ultrasound, cxr
Differential diagnosis
• Dermatofibroma
• melanocytic nevus
• ecchymosis
• granuloma annulare
• insect bite reactions
Management
• Radiotherapy
• Cryosurgery
• Photodynamic Therapy
• Excisional Surgery
• Intralesional Cytotoxic Chemotherapy
• Chemotherapy- single and combined
chemotherapy
If you’re not infected
you’re affected

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Kaposi sarcoma

  • 2. Introduction • A multifocal systemic tumor of endothelial cell origin. • linked with human herpesvirus 8 infection • Has Four clinical variants • Responds to radiation and chemotherapy,
  • 3. Clinical variants of KS • classic KS • endemic African KS • immunosuppressive therapy–related KS • HIV/AIDS-related KS
  • 4. Classic KS • Occurs in elderly males of eastern European heritage. • Predominantly arises on the legs but also occurs in lymph nodes and abdominal viscera. • slow progression and has good prognosis
  • 5. African-Endemic KS • bimodal age distribution young adults, mean age 35; and young children, mean age 3 years • Males > females • Has poor prognosis (young adults 5–8 years; young children 2–3 years) • Four clinical patterns
  • 6. African-Endemic KS patterns a) Nodular type: benign course and resembles classic KS. b) Florid or vegetating type: more aggressive. Nodular extend deeply into the subcutis, muscle, and bone. c) Infiltrative type: more aggressive has mucocutaneous and visceral . d) Lymphadenopathic type: children and young adults. confined to lymph nodes and viscera, also involves the skin and mucous membrane.
  • 7. Iatrogenic Immunosuppression- Associated KS • Rare. • Most commonly in solid-organ transplant recipients • chronic use of immunosuppressive drugs • Resolves on cessation of immunosuppression.
  • 8. HIV/AIDS-Associated KS • AIDS increases risk of KS ( 20,000 times that those not infected with HIV) • Common in homosexual men • Rapid progression, extensive systemic involvement • KS of the bowel and/or lungs is responsible for numerous deaths
  • 9. Pathogenesis • Initially polyclonal proliferation is due angiogenic factors. • Later becomes monoclonal. • KS lesions produce growth factors. • It is not know how HHV8 promotes the process.
  • 10. Clinical manifestation • Mucocutaneous lesions are usually asymptomatic • lower extremities - edema and moderate to severe pain • Urethral or anal canal lesions- obstruction • Pulmonary KS - bronchospasm, intractable coughing, shortness of breath, progressive respiratory failure.
  • 11. Skin lesions ecchymotic- like macule patches papules, plaques nodules tumours The lesions are normally palpable even at the patch stage.
  • 13.
  • 16. Investigations • Skin biopsy- Vascular channels lined by atypical endothelial cells. - extravasated erythrocytes with hemosiderin deposition Imaging – abdominal ultrasound, cxr
  • 17. Differential diagnosis • Dermatofibroma • melanocytic nevus • ecchymosis • granuloma annulare • insect bite reactions
  • 18. Management • Radiotherapy • Cryosurgery • Photodynamic Therapy • Excisional Surgery • Intralesional Cytotoxic Chemotherapy • Chemotherapy- single and combined chemotherapy
  • 19. If you’re not infected you’re affected