Kaposiform Hemangioendothelioma
Steven D. Billings, MD
Key Facts
Clinical Issues
Presents in infants and young children
Deep tumors, often multiple nodules
Associated with Kasabach-Merritt phenomenon (especially retroperitoneal tumors)
Consumptive coagulopathy
Thrombocytopenia
Rare regional lymph node metastases
No distant metastases reported to date
Mortality approximately 10%, related to local effects of tumor or Kasabach-Merritt phenomenon
Microscopic Pathology
Spindled cell areas resembling Kaposi sarcoma
Zones resembling capillary hemangiomas
Minimal atypia
Immunohistochemistry shows positive CD31, CD34, FLI-1, and podoplanin staining
Negative for HHV8
Clinical photograph shows a large inguinal tumor in an infant. More superficial tumors typically present as an erythematous or violaceous mass. |
ETIOLOGY/PATHOGENESIS
Developmental Anomaly
Approximately 1/2 of kaposiform hemangioendothelioma cases present in 1st year of life
CLINICAL ISSUES
Epidemiology
Age
Majority present in childhood to teen years
Presentation
Painful or painless mass
Presents as superficial or deep massStay updated, free articles. Join our Telegram channel
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