Nathan Nirmal, Thaller Seth R
Miller School of Medicine at the University of Miami, Miami, Florida 33131, USA.
J Craniofac Surg. 2006 Jul;17(4):724-8. doi: 10.1097/00001665-200607000-00024.
Sturge-Weber syndrome (SWS), Klippel-Trenaunay syndrome (KTS), and Parkes-Weber syndrome (PWS) represent a wide range of congenital vascular abnormality syndromes. Although many of the diagnostic criteria overlap for these syndromes, there are important differences among these diseases that carry important prognostic and therapeutic implications. This review attempts to clearly distinguish among SWS, KTS, and PWS, although loosely categorizing them as a family of congenital vascular disorders. A review of literature reveals that a variety of diagnostic tools exist that can help differentiate between the syndromes and assess risk for certain complications, which may help tailor various treatment modalities for a particular patient.
斯特奇-韦伯综合征(SWS)、克-特综合征(KTS)和帕克斯-韦伯综合征(PWS)代表了一系列先天性血管异常综合征。尽管这些综合征的许多诊断标准相互重叠,但这些疾病之间存在重要差异,具有重要的预后和治疗意义。本综述试图明确区分SWS、KTS和PWS,尽管将它们大致归类为先天性血管疾病家族。文献综述表明,存在多种诊断工具,可帮助区分这些综合征并评估某些并发症的风险,这可能有助于为特定患者量身定制各种治疗方式。