1例婴儿Klippel-Trenaunay-Weber综合征报告  

Klippel-Trenaunay-Weber syndrome: a case report

作　　者：廖贻雨 韦拔 蒋永江 韦义军 甘源 LIAO Yi-yu;WEI Ba;JIANG Yong-jiang(Department of Neonatology,Liuzhou Maternal and Child Health-Care Hospital,Liuzhou 545001,China)

机构地区：[1]柳州市妇幼保健院新生儿科

出　　处：《中国实用医药》2019年第31期125-126,共2页China Practical Medicine

摘　　要：本文回顾性分析1例婴儿Klippel-Trenaunay-Weber综合征的临床症状、体征及诊治过程.Klippel-Trenaunay-Weber综合征大多数是由于自发性突变所致,骨、血管异常病变,临床症状表现为血管畸形、静脉曲张、骨和(或)软组织肥大.早产儿发生Klippel-Trenaunay-Weber更隐匿,需要认真查体、密切观察,避免漏诊漏治.This paper retrospectively analyzed the clinical symptoms,signs and course of diagnosis and treatment of an infant with Klippel-Trenaunay-Weber syndrome.Klippel Trenaunay Weber syndrome is mainly caused by spontaneous mutation.The clinical symptoms of the disease are vascular malformation,varicose vein,and hypertrophy of bone and/or soft tissue.Klippel Trenaunay Weber is more insidious in preterm infants,which requires careful physical examination and close observation to avoid missed diagnosis and treatment.

关 键 词：婴儿Klippel-Trenaunay-Weber综合征 肢体肥大 血管畸形 

分 类 号：R72[医药卫生—儿科]