| Literature DB >> 20863161 |
Israel Fernandez-Pineda1, Juan Carlos Lopez-Gutierrez, Gema Ramirez, Catalina Marquez.
Abstract
Kasabach-Merritt phenomenon (KMP) is a serious coagulopathy with severe thrombocytopenia (<10,000/mm³) that occurs in the presence of an enlarging vascular tumor such as kaposiform hemangioendothelioma (KHE) and tufted angioma (TA). The natural history and treatment of these lesions remain controversial. The authors report a KHE case and a TA case that presented with KMP, describing their successful pharmacological management with vincristine, ticlopidine, and aspirin.Entities:
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Year: 2010 PMID: 20863161 DOI: 10.3109/08880018.2010.508299
Source DB: PubMed Journal: Pediatr Hematol Oncol ISSN: 0888-0018 Impact factor: 1.969