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Title: Severe hemorrhage complicating the Klippel-Trénaunay-Weber syndrome. Author: Aronoff DM, Roshon M. Journal: South Med J; 1998 Nov; 91(11):1073-5. PubMed ID: 9824196. Abstract: The Klippel-Trénaunay-Weber (KTW) syndrome is a congenital disorder of angiogenesis characterized by macular nevus, skeletal and soft tissue hypertrophy, venous varicosities, and arteriovenous fistulas. Disseminated intravascular coagulation (DIC) and the Kasabach-Merritt syndrome, a consumptive coagulopathy with thrombocytopenia, are both associated with the KTW syndrome. We describe a 30-year-old woman with KTW syndrome and Kasabach-Merritt syndrome who had DIC with severe hemorrhage after a routine gynecologic procedure. The bleeding was controlled with the use of intravenous low-dose heparin and antithrombin III.[Abstract] [Full Text] [Related] [New Search]