Author(s): Haraki I*, El Yazal S, Ait Errami A, Lairani FZ, Jiddi S, Samlani Z, Krati K and Oubaha S
Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder, characterized by the triad of vascular malformations (angioma), venous and or lymphatic malformations and asymmetrical disturbed growth of soft tissues and/or bone. Primary rectal linitis is a rare digestive tumor with very poor prognosis. We report the case of a 41-year-old patient with Klippel trenaunay ...