Unusual association of two rare entities: Primary rectal linitis and Klippel-Trenaunay syndrome

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 syndrome who was diagnosed with primary rectal linitis. 

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Published on: Jan 17, 2019 Pages: 1-2

Full Text PDF Full Text HTML DOI: 10.17352/2455-2283.000059
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