Kasabach-Merritt Phenomenon

  • Kasabach-Merritt Phenomenon (KMP) is a rare consumptive coagulopathy that can be seen with rapidly enlarging vascular tumours 1, such as Kaposiform hemangioepitheliomas.
    • It is thought to be due to sequestration of platelets and clotting factors within the the lesion resulting in disseminated intravascular coagulation.
  • Treatment is directed towards (1) maintaining hemostasis and (2) addressing the underlying tumor.2
    • Transfusion of platelets or FFP should be administered due to symptoms (such as bleeding), and not based on laboratory values alone.
    • Treatment modalities targeting the tumour include medical therapy (corticosteroids, interferon alpha, vincristine), embolization, or surgical excision.
  1. Kasabach HH, Merritt KK. Capillary hemangioma with extensive purpura. Am J Dis Child 1940;59:1063–79. 

  2. Kelly, Michael. “Kasabach-merritt phenomenon.” Pediatric Clinics 57.5 (2010): 1085-1089. 

Last updated October 10, 2022