Fernandez-Pineda Israel, Lopez-Gutierrez Juan Carlos, Ramirez Gema, Marquez Catalina
Department of Pediatric Surgery, Virgen del Rocio Children's Hospital, Sevilla, Spain.
Pediatr Hematol Oncol. 2010 Nov;27(8):641-5. doi: 10.3109/08880018.2010.508299.
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.
卡萨巴赫-梅里特现象(KMP)是一种严重的凝血病,伴有严重血小板减少(<10,000/mm³),发生于诸如卡波西样血管内皮瘤(KHE)和丛状血管瘤(TA)等不断增大的血管肿瘤存在时。这些病变的自然病程和治疗仍存在争议。作者报告了1例表现为KMP的KHE病例和1例TA病例,描述了使用长春新碱、噻氯匹定和阿司匹林对其进行成功药物治疗的情况。