首页> 美国卫生研究院文献>Journal of Cardiothoracic Surgery >Innominate truncal and arch blowout with left hemiparesis and right hemothorax followed by delayed cheese-wire perforation of innominate graft
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Innominate truncal and arch blowout with left hemiparesis and right hemothorax followed by delayed cheese-wire perforation of innominate graft

机译:无名的躯干和足弓爆裂伴左偏瘫和右胸腔血随后无名移植物的干酪丝穿孔延迟

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摘要

We present the case of a 68 year old Caucasian woman, in extremis, with left hemiparesis and right hemothorax, in hypovolemic shock, secondary to a blow-out of a large penetrating ulcer at the junction of innominate trunk and aortic arch. She underwent interposition graft replacement of innominate trunk and repair of aortic arch, on cardiopulmonary bypass, employing total circulatory arrest and selective antegrade cerebral perfusion and had total resolution of hemiparesis. She, however, represented, 6 months later, with threatened exsanguination after a sternal wire cheese-wired through the sternum and perforated the anteriorly lying innominate graft. Following successful repair, she was found to have an old intramural hematoma of distal arch and descending thoracic aorta and changes suggestive of chronic dissection of the whole of abdominal aorta. This was managed conservatively.We believe this patient’s presentation initially with a spontaneous innominate blow-out, cardiogenic shock, hemothorax and hemiparesis, and later with cheese-wire perforation of the innominate graft is unique. Her surgical rescue at both presentations was equally unusual, and without surgical precedent to the best of our knowledge. Was the initial innominate blow-out the result of localised innominate dissection, or more unusually, part of retrograde descending thoracic dissection with skip penetration of innominate artery and sparing of the intervening arch? Was it secondary to the minor fall she had sustained 1 week prior to the event, resulting in a false aneurysm or a contained hematoma next to the innominate artery? More intriguingly, did diffuse aortopathy underpin these diverse etiologies and result in penetrating intimal ulcer with blow out in the innominate artery, intramural hematoma in the arch and descending thoracic aorta and dissection in abdominal aorta at different points in time?We review the current literature for these unusual afflictions of innominate trunk and its origin from the arch of aorta.
机译:我们提出了一个68岁的白人妇女的案例,该患者的肢体有左偏瘫和右血胸,伴有低血容量性休克,其继发于无名的躯干和主动脉弓交界处的大穿透性溃疡。她在体外循环下进行了无名主干的介入移植物置换和主动脉弓的修复,采用了总循环停止和选择性顺行性脑灌注,并完全治愈了偏瘫。然而,她表示,六个月后,胸骨钢丝穿过胸骨并穿刺了位于前侧的无名移植物后,威胁要放血。成功修复后,发现她患有远端弓和降主动脉的壁内旧血肿,其变化提示整个腹主动脉的慢性解剖。我们对此采取了保守的处理方法。我们认为,该患者最初的表现为自发性无症状性心律失常,心源性休克,血胸和偏瘫,后来无创性移植物采用干酪丝穿孔是独特的。在这两次演讲中,她的外科手术救助同样是不寻常的,并且就我们所知,还没有手术先例。最初的无名爆胎是局部无名解剖的结果,或更常见的是部分倒回的胸廓下行解剖,无名动脉的跳跃穿透和中间弓的保留吗?它是在事件发生前1周持续的轻微跌倒继发于人,导致假动脉瘤或在无名动脉旁出现了血肿吗?更有趣的是,弥漫性主动脉病是否支持这些多样的病因,并导致内膜溃疡穿透,无名动脉吹出,弓内壁内血肿,降主动脉降主动脉和腹主动脉在不同时间点解剖?这些不寻常的躯干折磨及其起源于主动脉弓。

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