Hemangioma-Thrombocytopenia Syndrome
- 1 January 1975
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 111 (1) , 105-107
- https://doi.org/10.1001/archderm.1975.01630130107016
Abstract
A patient who had multiple hemangiomas and for whom results of coagulation studies were consistent with the hemangioma-thrombocytopenia (Kasabach-Merritt) syndrome and a microangiopathic hemolytic process was asymptomatic prior to surgical removal of a lipoma. Postoperatively, she developed bleeding secondary to a disseminated intravascular coagulopathy. Her bleeding was controlled by anticoagulation therapy. A review of the literature provides evidence suggesting that the hemangioma-thrombocytopenia syndrome is due to a disseminated intravascular coagulopathy initiated within the hemangioma. Surgical trauma may precipitate exacerbations of the coagulopathy in these patients and all unnecessary surgical procedures should be avoided.Keywords
This publication has 9 references indexed in Scilit:
- Disseminated Intravascular Coagulation (DIC)Kafkas Universitesi Veteriner Fakultesi Dergisi, 2007
- Platelet and Fibrinogen Consumption in ManNew England Journal of Medicine, 1972
- Pathology of disseminated intravascular coagulation (DIC)Human Pathology, 1972
- The Clinical Challenge of Disseminated Intravascular CoagulationNew England Journal of Medicine, 1970
- Chronic defibrination syndrome due to a giant hemangioma associated with microangiopathic hemolytic anemiaThe American Journal of Medicine, 1969
- Acquired Hypofibrinogenemia Associated with a Giant Cavernous Hemangioma of the LiverAmerican Journal of Clinical Pathology, 1963
- Hemangioma associated with thrombocytopenia: Report of a case and review of the literatureThe American Journal of Medicine, 1962
- Giant Vascular Tumors and ThrombocytopeniaArchives of Dermatology, 1960
- CAPILLARY HEMANGIOMA WITH EXTENSIVE PURPURAAmerican Journal of Diseases of Children, 1940