May-Thurner syndrome associated with Klippel-Trenaunay syndrome.

Tony Lu, Eileen de Grandis, Peter Gloviczki, James Glockner, Roger F Shepherd
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引用次数: 7

Abstract

We present an unusual case of a 23-year-old man who had symptomatic lower extremity varicosities that have been present since birth. He was complaining of pain and swelling of several years duration. Evaluation revealed Klippel-Trenaunay syndrome with associated compression of the left common iliac vein by the overriding left common iliac artery (May-Thurner syndrome). The patient was treated with left common iliac vein stenting followed by high ligation and inversion stripping of his grossly incompetent left small saphenous vein, stripping of his aberrant left lateral embryonic veins, and also by multiple stab phlebectomies, with excellent early result.

May-Thurner综合征与Klippel-Trenaunay综合征相关。
我们提出一个不寻常的情况下,一个23岁的男子谁有症状下肢静脉曲张,已经存在,因为出生。他主诉疼痛和肿胀持续了好几年。评估显示Klippel-Trenaunay综合征伴有左髂总静脉被覆盖的左髂总动脉压迫(May-Thurner综合征)。患者行左髂总静脉支架置入术,随后高位结扎并倒置剥离其严重不正常的左小隐静脉,剥离其异常的左外侧胚胎静脉,并多次穿刺静脉切除术,早期效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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