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A case of neonatal arterial thrombosis mimicking interrupted aortic arch

机译:新生儿动脉血栓形成模仿主动脉弓破裂1例

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摘要

Neonatal arterial thrombosis is a very rare entity with clinical findings resembling coarctation of aorta or interrupted aortic arch. A two day-old male newborn was admitted to a different hospital with difficulty in sucking and sleepiness. On echocardiographic examination, a diagnosis of interrupted aortic arch was made and he was treated with prostoglandin E2. When the patient presented to our center, physical examination revealed that his feet were bilaterally cold. The pulses were not palpable and there were ecchymotic regions in the lower extremities. Echocardiography ruled out interrupted aortic arch. Computerized tomographic angiography revealed a large thrombosis and total occlusion of the abdominal aorta. Since there was no response to treatment with tissue plasminogen activator, we performed thrombectomy. Homozygous Factor V Leiden and Methylenetetrahydrofolate reductase mutations were found in this patient. Neonatal aortic thrombosis which is observed very rarely and fatal should be considered in the differential diagnosis of coarctation of aorta and interrupted aortic arch.
机译:新生儿动脉血栓形成是一种非常罕见的实体,其临床表现类似于主动脉缩窄或主动脉弓断裂。两天大的男性新生儿因吸吮和嗜睡困难而被送往另一家医院。在超声心动图检查中,诊断为主动脉弓中断,并接受了prostoglandin E2治疗。当患者到我们中心就诊时,体格检查发现他的脚双侧发凉。脉搏不明显,下肢有瘀斑。超声心动图检查排除了主动脉弓中断。电脑断层血管造影显示腹部大动脉血栓形成和完全闭塞。由于对组织纤溶酶原激活剂的治疗没有反应,我们进行了血栓切除术。在该患者中发现纯合因子V Leiden和亚甲基四氢叶酸还原酶突变。新生儿主动脉血栓形成很少见且致命,应在主动脉缩窄和主动脉弓缩窄的鉴别诊断中考虑。

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