Jang Seo Jin, Han Yoonhee, Kwon Jae Hyun
Taehan Yongsang Uihakhoe Chi. 2020 Nov;81(6):1517-1522. doi: 10.3348/jksr.2020.0029. Epub 2020 Oct 19.
Persistent sciatic artery (PSA), a rare congenital vascular anomaly, increases susceptibility to aneurysms and accounts for 40-61% of the cases. Here, we describe a case of PSA in a 70-year-old man with a history of alcoholic liver cirrhosis. Bilateral complete PSAs were detected incidentally on computed tomography angiography during evaluation for spontaneous intramuscular bleeding in the thigh due to cirrhosis-related coagulopathy. Selective angiography of the left PSA revealed aneurysmal dilatation and thrombotic occlusion of the PSA, which was partially removed with aspiration thrombectomy. Intramuscular bleeding was succesfully managed with empirical embolization of the deep femoral artery.
持续性坐骨动脉(PSA)是一种罕见的先天性血管异常,会增加动脉瘤的易感性,占病例的40%-61%。在此,我们描述一例70岁男性的PSA病例,该患者有酒精性肝硬化病史。在因肝硬化相关凝血病导致大腿自发性肌肉出血而进行评估期间,计算机断层血管造影偶然发现双侧完全性PSA。左侧PSA的选择性血管造影显示PSA有动脉瘤样扩张和血栓形成性闭塞,通过抽吸血栓切除术部分清除了血栓。通过对股深动脉进行经验性栓塞成功处理了肌肉出血。