漂浮的升主动脉血栓伴有抗磷脂综合征:一份病例报告。

Shinya Tajima, Tomoaki Kudo, Daisuke Mori, Katsukiyo Kitabayashi
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引用次数: 0

摘要

背景:升主动脉血栓是一种可导致致命血栓栓塞的罕见疾病。该病的治疗方法尚不明确,取决于外科医生的临床经验。大多数关于抗磷脂综合征(APS)血栓形成的报道都与静脉或外周动脉血栓形成有关,几乎没有关于主动脉血栓形成的报道:一名 74 岁的男性因左腿跛行 3 个月而被转诊至我科。计算机断层扫描血管造影术(CTA)和经胸超声心动图检查显示,升主动脉腔内有一个与 APS 相关的漂浮和有蒂的肿块,左股浅动脉有栓塞。在深低温循环停滞状态下,我们切除了漂浮的肿块,但没有更换移植物。术后 1 年的 CTA 显示血栓没有复发:我们经历了一例罕见的漂浮升主动脉血栓。结论:我们经历了一例罕见的漂浮的升主动脉血栓,我们认为漂浮的升主动脉血栓伴有栓塞事件时应进行手术干预。
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Floating ascending aortic thrombus with antiphospholipid syndrome: a case report.

Background: Ascending aortic thrombus is a rare disease that can cause fatal thromboembolism. The treatment for the disease is not well defined and depends on the clinical experience of surgeons. Most reports of thrombosis in antiphospholipid syndrome (APS) are associated with venous or peripheral arterial thrombosis, and there are almost no reports of thrombosis of the aorta.

Case presentation: A 74-year-old male was referred to our department with claudication of the left leg lasting 3 months. A computed tomography angiography (CTA) and a transthoracic echocardiography demonstrated that a floating and pedunculated mass associated with APS was located at ascending aortic lumen and an embolism in the left superficial femoral artery. Under deep hypothermic circulatory arrest, we resected a floating mass without the graft replacement. CTA 1 year after surgery showed no recurrence of thrombus.

Conclusion: We experienced a rare case of floating ascending aortic thrombi. As in this case, we consider that a floating ascending aortic thrombus with embolic events should be performed by surgical intervention.

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