导致肺栓塞的下腔静脉发育不良:病例报告和文献综述。

Juan Felipe Coronado-Sarmiento, Christian Eduardo Rey-Ramos
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摘要

导言:下腔静脉缺如(IVCA)是一种非常罕见的血管疾病,发病率约占总人口的0.0005%至1%。作为深静脉血栓和肺栓塞的潜在病因,它常常被忽视,尤其是在年轻患者中:一名 25 岁的西班牙裔女性因腿部肿胀和疼痛到急诊科就诊。随后,她出现呼吸急促和胸痛,被转入重症监护室。胸部和腹部计算机断层扫描血管造影证实了左肺栓塞、肾下腔静脉缺失以及左侧髂浅静脉和股静脉血栓。她接受了溶栓治疗,随后成功进行了血栓切除术:IVCA是一种罕见的血管疾病,由下腔静脉发育不良或血栓形成继发吸收引起。这导致侧支静脉系统复杂,血流缓慢,增加了瘀血和血栓形成的风险。对于缺乏典型风险因素、反复发生血栓栓塞的年轻患者,应考虑进行 IVCA。最好通过计算机断层扫描或磁共振血管造影进行诊断。治疗方法通常包括长期抗凝,并为特定病例保留手术治疗:结论:IVCA是血栓栓塞事件的一个不常见原因。重要的是,在排除免疫、遗传或外伤问题后,年轻患者应考虑这一诊断,因为及时治疗有助于防止严重的健康风险。
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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Inferior Vena Cava Agenesis as Cause of Pulmonary Embolism: Case Report and Literature Review.

Introduction: Inferior vena cava agenesis (IVCA) is a very uncommon vascular condition, occurring in about 0.0005% to 1% of the population. It is often overlooked as a potential cause of deep venous thrombosis and pulmonary embolism, particularly in younger patients.

Case presentation: A 25-year-old Hispanic woman presented to the emergency department with leg swelling and pain. She later developed shortness of breath and chest pain, prompting her transfer to the intensive care unit. Chest and abdominal computed tomographic angiography confirmed a left pulmonary embolism, absence of the infrarenal vena cava, and a thrombus in the left superficial iliac and femoral veins. She was treated with thrombolytic therapy followed by a successful thrombectomy.

Discussion: IVCA is a rare vascular condition caused by either a developmental failure of the inferior vena cava or thrombosis with secondary resorption. This leads to a complex collateral venous system with slower blood flow, increasing the risk of stasis and thrombus formation. IVCA should be considered in young patients with recurrent thromboembolism who lack typical risk factors. Diagnosis is best achieved through computed tomography or magnetic resonance angiography. Management usually involves long-term anticoagulation, with surgery reserved for select cases.

Conclusions: IVCA is an uncommon cause of thromboembolism events. It is important to consider this diagnosis in young patients after immune, genetic, or traumatic issues have been ruled out, as prompt treatment can help prevent serious health risks.

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