梅-瑟纳综合征——广泛盆腔深静脉血栓的罕见病因,但还有更多需要了解的吗?

Case Reports in Vascular Medicine Pub Date : 2022-10-25 eCollection Date: 2022-01-01 DOI:10.1155/2022/7978470
Vikash Kumar, Michelle Koifman, Bhavyakumar Vachhani, Dhir Gala, Sumeet Bahl
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引用次数: 0

摘要

May-Thurner综合征(MTS)是一种罕见的解剖变异,其特征是右髂总动脉压迫左髂总动脉压迫第五腰椎。它可以表现为急性或慢性深静脉血栓(DVT)、腿部疼痛、静脉曲张、皮肤溃疡和色素沉着。在这个病例报告中,我们报告了一个有趣的病例,一名年轻男性,没有明显的危险因素,他表现为背部和左下肢疼痛,后来通过计算机断层血管造影(CTA)和静脉造影诊断为MTS。患者接受静脉成形术和药物力学溶栓治疗,出院时使用阿哌沙班。
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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May-Thurner Syndrome-a Rare Cause of Extensive Pelvic DVT, but Is there More to Know?

May-Thurner Syndrome (MTS) is a rare anatomical variant characterized by the compression of the left common iliac artery by the right common iliac artery against the fifth lumbar vertebrae. It can present as acute or chronic deep vein thrombosis (DVT), leg pain, varicosities, skin ulceration, and hyperpigmentation. In this case report, we present an interesting case of a young male with no obvious risk factors, who presented with back and left lower extremity pain later diagnosed with MTS on computed tomography angiography (CTA) and venogram. The patient was treated with venoplasty and pharmacomechanical thrombolysis and was discharged on apixaban.

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审稿时长
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