Bhadra Rajarshi, Somasundaram Meyappan, Iltchev Daniel V, Ravakhah Keyvan
Department of Internal Medicine, St. Vincent Charity Medical Center, Cleveland, Ohio, USA.
Department of Pulmonary and Critical Care Medicine, St. Vincent Charity Medical Center, Cleveland, Ohio, USA.
BMJ Case Rep. 2019 Apr 1;12(4):e227046. doi: 10.1136/bcr-2018-227046.
May-Thurner syndrome (MTS) is a clinical condition where the left common iliac vein gets compressed by the overlying right common iliac artery anterior to the fifth lumbar vertebra and the sacral promontory. It results in vessel wall injury and predisposition to thrombosis. We present a case of a 21-year-old African-American man with no significant past medical history who came to the emergency department with left lower limb swelling associated with shortness of breath, and was eventually diagnosed to have extensive left lower extremity deep vein thrombosis (DVT) along with acute bilateral extensive pulmonary embolism (PE) as a consequence to MTS. MTS should be considered in the differential when young patients present with unprovoked or recurrent left-sided DVT. Diagnosis of this anatomical variant is critical as it may need long-term anticoagulation and consideration of pharmaco-mechanical intervention such as mechanical thrombectomy and venoplasty with or without stenting.
梅-图二氏综合征(MTS)是一种临床病症,即左髂总静脉在第五腰椎和骶岬前方被上方的右髂总动脉压迫。这会导致血管壁损伤并易引发血栓形成。我们报告一例21岁非裔美国男性病例,其既往无重大病史,因左下肢肿胀伴呼吸急促前来急诊科就诊,最终被诊断为广泛的左下肢深静脉血栓形成(DVT)以及由MTS导致的急性双侧广泛肺栓塞(PE)。当年轻患者出现不明原因或复发性左侧DVT时,鉴别诊断应考虑MTS。诊断这种解剖变异至关重要,因为可能需要长期抗凝,并考虑进行药物机械干预,如机械血栓切除术和血管成形术,可选择或不选择置入支架。