<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vinall, Phil</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Guzmán, Ramona A. Lappot</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Patient Presenting with Nonpitting Edema Diagnosed with MTS</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2014-10-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">28-28</style></pages><abstract><style  face="normal" font="default" size="100%">May-Thurner syndrome (MTS), also known as Cockett syndrome or ileocaval compression syndrome, is a vascular anomaly first described in 1956 by R. May and J. Thurner. This syndrome frequently involves pain and significant swelling of the whole limb; however, not all patients present with symptoms, which can include left leg pain and edema, pulmonary embolism, deep vein thrombosis, varicose veins, and chronic ulcerations. This article presents a case of a male patient aged 16 years without past medical history who was referred to her practice after 10 months of pain and severe progressive nonpitting edema of the left leg.</style></abstract><number><style face="normal" font="default" size="100%">24</style></number><volume><style face="normal" font="default" size="100%">14</style></volume></record></records></xml>