Meine J G, Schwartz R A, Janniger C K
New Jersey Medical School, Newark 07103-2714, USA.
Cutis. 1997 Sep;60(3):127-32.
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue hypertrophy of an extremity. Recognition is usually possible during infancy or early childhood, and evaluation and treatment is important because morbidity may be minimized. We will review the clinical features, etiology, assessment, and treatment of patients with Klippel-Trenaunay-Weber syndrome.
克-特-韦综合征的特征为葡萄酒色斑、静脉曲张以及肢体的骨与软组织肥大三联征。通常在婴儿期或幼儿期即可识别,评估和治疗很重要,因为可将发病率降至最低。我们将对克-特-韦综合征患者的临床特征、病因、评估及治疗进行综述。