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May-Thurner Syndrome as a Rare Cause of Paradoxical Embolism in a Patient with Patent Foramen Ovale

机译:May-Thurner综合征是患有卵圆孔未闭患者的罕见悖论性栓塞的罕见原因

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摘要

May-Thurner syndrome is an underrecognized anatomical variant that can lead to increased propensity for venous thrombosis in the lower extremities. We present a case of a 67-year-old female who presented with transient ischemic attack. Initial workup including CT scan of the head, MRI scan of the head, and magnetic resonance angiogram of the head and neck was unremarkable. A transthoracic echocardiogram with bubble study was also normal. Subsequently, a transesophageal echocardiogram was performed that revealed a patent foramen ovale with right-to-left shunt. Lower extremity duplex venous ultrasound showed no evidence of deep vein thrombosis. However, magnetic resonance venogram of the pelvis showed compression of the left common iliac vein just after its origin suggestive of May-Thurner syndrome. Hence, May-Thurner syndrome was recognized as the probable source of paradoxical embolism causing transient ischemic attack in this patient.
机译:May-Thurner综合征是一种未被充分认识的解剖学变异,可导致下肢静脉血栓形成的倾向增加。我们介绍了一例67岁的女性,该女性出现短暂性脑缺血发作。最初的检查包括头颅CT扫描,头颅MRI扫描以及头颈磁共振血管造影均无统计学意义。经胸腔超声心动图与气泡研究也很正常。随后,经食管超声心动图检查发现卵圆孔未闭,右向左分流。下肢双工静脉超声未显示深静脉血栓形成的证据。然而,骨盆的磁共振静脉图显示刚好起源于May-Thurner综合征后,左侧common总静脉受压。因此,May-Thurner综合征被认为是引起该患者短暂性脑缺血发作的悖论性栓塞的可能来源。

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