换一批
换一批摘要Kasabach-Merritt现象(KMP)是快速生长的血管瘤伴消耗性凝血功能障碍的一类现象,多见于婴幼儿早期,好发于肢体远端、躯干部、腹膜后腔和颈部,其病死率高达30％.目前并无统一、有效的治疗方法.现综述KMP的病理生理学基础、诊断以及其治疗方法.
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abstractsKasabach-Merritt phenomenon (KMP) is characterized by thrombocytopenia with enlarging vascular tumour,KMP usually develops in infancy and is associated with significant morbidity and mortality,the mortality rate is reported as high as 30％.It commonly reported sites of tumor include extremities,trunk,retroperitoneum and neck.There is no consensus in treatment and various regimens have been used by different authors.This report is aim to learn the pathophysiology of the KMP and its diagnosis and treatment.
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关键词
Kasabach-Merritt现象血管瘤血小板减少消耗性凝血功能障碍卡波西血管内皮瘤簇状血管瘤Kasabach-Merritt phenomenonHemangiomaThrombocytopeniaConsumptive coagulopathyKaposiform hemangioendotheliomaTufted angioma
栏目名称
综述
DOI
10.3760/cma.j.issn.2095-428X.2014.10.018
发布时间
2019-01-11
基金项目
河南省科技攻关项目
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