Hansen T T, Boe S, Taudorf K
Acta Chir Scand. 1978;144(7-8):475-9.
Three cases of Klippel--Trenaunay--Weber's syndrome are presented. The syndrome is characterized by cutaneous hemangioma, hypertrophy of an extremity and varicose veins. It is combined with angiodysplasias, either in the form of aplasia/hypoplasia of deep veins and/or in the form of arteriovenous shunts. The varicose veins will frequently be the dominant symptom, and it is emphasized that surgical treatment should not be instituted until the patient has been examined angiographically, with both phlebography and arteriography. The methods and the classification are discussed and the possibilities of treatment are outlined.
本文报告了3例克-特-韦综合征。该综合征的特征为皮肤血管瘤、肢体肥大和静脉曲张。它常合并血管发育异常，表现为深静脉发育不全/发育不良和/或动静脉分流。静脉曲张常为主要症状，强调在对患者进行静脉造影和动脉造影的血管造影检查之前，不应进行手术治疗。文中讨论了治疗方法和分类，并概述了治疗的可能性。
