Unusual association of two rare entities: Primary rectal linitis and Klippel-Trenaunay syndrome
Journal: Archives of Clinical Gastroenterology (Vol.5, No. 1)Publication Date: 2019-02-26
Authors : Haraki I El Yazal S Ait Errami A Lairani FZ Jiddi S Samlani Z Krati K; Oubaha S;
Page : 001-002
Keywords : Primary; Rectal linitis; Klippel trenauney;
Abstract
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.
Other Latest Articles
- More than a common acid buffering in the treatment of Non-Erosive GERD-like Clinical Spectrum: A Chios Masthia-based Formulation with (Cyto) Protecting Effect
- Global Exponential Stabilization for a Class of Uncertain Nonlinear Control Systems Via Linear Static Control
- Survey on Security Threats in Cloud Computing
- A Study About Brand Preference of Washing Machine with Reference to Rural Area of Palanpur Taluka
- Modelling and Simulation of Some Combustion Parameters Intport-1 and Intvalve-1 using Gt-Power Engine Simulation Software with Biodiesel-Ethanol-Diesel Blends as Fuel
Last modified: 2019-04-12 16:47:09