Huiras Erin E, Barnes Cheryl J, Eichenfield Lawrence F, Pelech Andrew N, Drolet Beth A
Department of Pediatric Dermatology, Children's Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Pediatrics. 2005 Oct;116(4):e596-600. doi: 10.1542/peds.2004-1607. Epub 2005 Sep 15.
Klippel-Trenaunay syndrome (KTS) is a rare congenital anomaly characterized by unilateral limb overgrowth, venous varicosities, and capillary malformations (port wine stains) of the affected limb or limbs. Large venous malformations such as those observed in KTS are rare, and many physicians are unfamiliar with the potential complications, which include hypercoagulability, thrombosis, and pulmonary embolism (PE). As a result, patients may suffer from delayed diagnosis of a potentially life-threatening thromboembolic event. We present 2 cases of children with KTS complicated by PE, and we review the English-language literature regarding pathophysiologic features, interventions, and outcomes of PE in the setting of KTS among both pediatric and adult patients, with emphasis on issues relevant to pediatricians.
克-特综合征(KTS)是一种罕见的先天性异常疾病,其特征为患侧单肢或多肢出现肢体过度生长、静脉曲张以及毛细血管畸形(葡萄酒色斑)。在KTS中观察到的大型静脉畸形较为罕见,许多医生对其潜在并发症并不熟悉,这些并发症包括高凝状态、血栓形成和肺栓塞(PE)。因此,患者可能会因潜在的危及生命的血栓栓塞事件而被延迟诊断。我们报告2例并发PE的KTS患儿病例,并回顾了关于儿科和成年患者KTS合并PE的病理生理特征、干预措施及预后的英文文献,重点关注与儿科医生相关的问题。