Metsvaht Tuuli, Hermlin Toomas, Kern Hartmut, Kahre Tiina, Starkopf Joel
Clinic of Anesthesiology and Intensive Care, Tartu University Clinics, Tartu, Estonia.
Congenit Heart Dis. 2006 Jan;1(1-2):40-5. doi: 10.1111/j.1747-0803.2006.00007.x.
Neonatal spontaneous aortic arch thrombosis without an anatomical correlate is an extremely rare disorder of unknown etiology. A 1-day-old newborn was admitted with suspicion of the coarctation of the aorta. Angiography revealed congenital occluding thrombosis of the ascending aorta and the aortic arch. Surgery was considered impossible because of concomitant thrombosis of the inferior vena cava and the right renal vein. Thrombolysis with streptokinase and tissue plasminogen activator was attempted unsuccessfully. Heterozygous carrier status of the factor V Leiden mutation was diagnosed as a single prothrombotic risk factor. Congenital prothrombotic conditions including factor V Leiden carrier status may serve as risk factors for the development of spontaneous aortic arch thrombosis in neonates. In chronic organized thrombi thrombolytic therapy is likely to fail.
新生儿自发性主动脉弓血栓形成且无解剖学相关因素是一种病因不明的极其罕见的疾病。一名1日龄新生儿因怀疑主动脉缩窄入院。血管造影显示升主动脉和主动脉弓先天性闭塞性血栓形成。由于下腔静脉和右肾静脉同时存在血栓形成,认为无法进行手术。尝试使用链激酶和组织纤溶酶原激活剂进行溶栓治疗,但未成功。诊断出因子V莱顿突变的杂合子携带者状态为单一的血栓形成前危险因素。包括因子V莱顿携带者状态在内的先天性血栓形成前状况可能是新生儿自发性主动脉弓血栓形成发展的危险因素。在慢性机化血栓中,溶栓治疗很可能失败。