ISSN: 2455-2283 Clinical Group

Archives of Clinical Gastroenterology  Open Access

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

    DOI Logo 10.17352/2455-2283.000059

    Published On: January 17, 2019 | Pages: 001 - 002

    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 ...
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