Aortic Dissection Involving a Right Retroesophagian Subclaviary Artery (LUSORIA) Associated with a Bi-Carotidian Trunk: About a Case at the National University Hospital Center of Fann (Sénégal)

Sarr El Hadj Mbacké, Khaddra H, Manga Simon Joël, Seye Modou, D. Momar, B. Md, S. Lamine, Bindia Dominique, Sarr Ndeye Aramec, Tine Elisabeth Arame, Diallo Arame Diagne, Ba Kadia, Dièye Ousmane, D. Bara
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Abstract

The lusoria artery is a rare congenital vascular anomaly involving most of the time the right subclavian artery. It can also be associated with a serious vascular pathology such as aortic dissection although this phenomenon is not common in the literature and most often requires rather complex surgical management because of the layout of this artery. We report a discovery of a lusoria artery case revealed by aortic dissection. This is a 63-yearold patient with recently discovered hypertension as a cardiovascular risk factor. He was received for severe chest pain. Clinical examination found grade III systolo-diastolic hypertension and tachycardia. The thoracic CT angiography found an aspect of type B aortic dissection associated with an aberrant right subclavian artery of the lusoria type. In emergency, the patient had benefited from an antihypertensive treatment allowing stabilizing his high blood pressure. The development during hospitalization was favorable with a disappearance of the pain and a stabilization of his blood pressure levels. His discharge was made on D10 of hospitalization with a transfer to a cardiovascular surgery center for better treatment.
右后食道锁骨下动脉(LUSORIA)合并双颈动脉主干的主动脉夹层:关于范恩国立大学医院中心的一例病例
卢索里亚动脉是一种罕见的先天性血管异常,大部分时间涉及右锁骨下动脉。它也可能与严重的血管病理有关,如主动脉夹层,尽管这种现象在文献中并不常见,而且由于该动脉的布局,通常需要相当复杂的手术管理。我们报告了一例通过主动脉夹层发现的卢索里亚动脉病例。这是一名63岁的患者,最近发现高血压是心血管危险因素。他因严重胸痛而入院治疗。临床检查发现III级收缩期-舒张期高血压和心动过速。胸部CT血管造影术发现B型主动脉夹层与卢索里亚型异常右锁骨下动脉相关。在紧急情况下,患者受益于降压治疗,从而稳定了他的高血压。住院期间的病情发展良好,疼痛消失,血压水平稳定。他在住院D10出院,并被转移到心血管外科中心接受更好的治疗。
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