Klippel-Trenaunay-Weber Syndrome – A Rare Case with Visceral Manifestation and Thrombosed Marginal Vein of Servelle

Abstract

Klippel-Trenaunay-Weber syndrome is a rare congenital syndrome characterized by capillary, venous or lymphaticmalformation and hemihypertrophy. Only 1000 cases of this syndrome have been reported in the literature. A rare case of this syndrome is presented here, who presented with its visceral and vascular complications and was diagnosed for the first time.