Hng Joel, Su Shu, Atkinson Noel
Department of Vascular Surgery, The Royal Melbourne Hospital, 300 Grattan Street, Parkville, VIC, 3050, Australia.
Department of Radiology, The Royal Melbourne Hospital, 300 Grattan Street, Parkville, VIC, 3050, Australia.
J Med Case Rep. 2021 Mar 19;15(1):141. doi: 10.1186/s13256-021-02730-8.
May-Thurner syndrome is an anatomical condition characterized by compression of the left common iliac vein by the right common iliac artery, causing venous outflow obstruction. It is an uncommon cause of deep vein thrombosis and is more prevalent among women. This paper highlights the importance of considering May-Thurner syndrome in young males without risk factors presenting with left lower limb pain, as endovascular treatment may be required.
A 23 year-old Caucasian male presented with a 1-week history of left lower limb pain, edema, and pallor. He was found to have an unprovoked deep vein thrombosis on Doppler ultrasound involving the left fibular, soleus, gastrocnemius, popliteal, femoral, common femoral, and external iliac veins. A heparin infusion was commenced as the initial treatment for deep vein thrombosis. Further investigation with computer tomography pulmonary angiogram and computer tomography venography of the abdomen and pelvis showed bilateral pulmonary emboli and left common iliac vein compression with left common, internal, and external iliac vein thrombosis. He was diagnosed with May-Thurner syndrome despite having no risk factors. A retrievable Cook Celect Platinum inferior vena cava filter was placed, and thrombus of the left common femoral, external, and common iliac veins was treated successfully with AngioJet thrombectomy, thrombolysis using 200,000 units of urokinase, angioplasty and stenting using two Cook Zilver Vena venous self-expanding stents. Therapeutic enoxaparin was commenced on discharge. His filter was removed after 10 weeks. Hematological follow-up 4 months later showed an overall negative thrombophilia screen, and anticoagulation was switched to apixaban. He has had no recurrent thrombosis.
Clinicians should have a low threshold to investigate for May-Thurner syndrome in patients with left lower limb venous thrombotic events regardless of risk factors, as endovascular treatment may be required to minimize the long-term sequelae of deep vein thrombosis. Duplex ultrasound can be used initially for diagnosis, and computer tomography venography used subsequently if the common iliac vein is not visualized on ultrasound. Endovascular treatment is preferred over anticoagulation alone, especially in otherwise fit patients presenting early, the aim being to reduce the chances of chronic venous hypertension in the lower limb.
梅-图二氏综合征是一种解剖学状况,其特征为右髂总动脉压迫左髂总静脉,导致静脉流出道梗阻。它是深静脉血栓形成的一种罕见病因,在女性中更为常见。本文强调了对于无危险因素但出现左下肢疼痛的年轻男性考虑梅-图二氏综合征的重要性,因为可能需要进行血管内治疗。
一名23岁的白种男性,有1周的左下肢疼痛、水肿和苍白病史。经多普勒超声检查发现其患有不明原因的深静脉血栓形成,累及左腓静脉、比目鱼肌静脉、腓肠肌静脉、腘静脉、股静脉、股总静脉和髂外静脉。开始静脉输注肝素作为深静脉血栓形成的初始治疗。进一步的计算机断层扫描肺动脉造影以及腹部和盆腔计算机断层扫描静脉造影显示双侧肺栓塞以及左髂总静脉受压伴左髂总静脉、髂内静脉和髂外静脉血栓形成。尽管他没有危险因素,但仍被诊断为梅-图二氏综合征。置入了可回收的库克Celect Platinum下腔静脉滤器,采用AngioJet血栓切除术成功治疗了左股总静脉、髂外静脉和髂总静脉的血栓,使用20万单位尿激酶进行溶栓,并使用两个库克Zilver Vena静脉自膨式支架进行血管成形术和支架置入术。出院时开始使用治疗剂量的依诺肝素。10周后取出了他的滤器。4个月后的血液学随访显示血栓形成倾向筛查总体为阴性,抗凝治疗改为阿哌沙班。他没有复发血栓形成。
临床医生对于左下肢静脉血栓形成事件的患者,无论有无危险因素,都应降低对梅-图二氏综合征进行检查的阈值,因为可能需要进行血管内治疗以将深静脉血栓形成的长期后遗症降至最低。最初可使用双功超声进行诊断,如果超声未显示髂总静脉,则随后可使用计算机断层扫描静脉造影。血管内治疗优于单纯抗凝治疗,尤其是对于早期就诊的其他情况良好的患者,目的是降低下肢慢性静脉高压的发生几率。