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采用去分支及动脉瘤切除术治疗的无症状性迷走动脉巨大动脉瘤。

Asymptomatic Giant Aneurysm of the Arteria Lusoria Treated by Debranching and Aneurysmal Resection.

作者信息

Venkatesan Aadithiyavikram, Gonuguntla Akhilesh, Vasireddy Anila, Rai Guruprasad D, Kamath Ganesh Sevagur, Bishnoi Arvind Kumar, Maramreddy Revanth

机构信息

Department of Cardiovascular and Thoracic Surgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.

出版信息

Vasc Specialist Int. 2022 Mar 21;38:3. doi: 10.5758/vsi.210069.

Abstract

The aberrant right subclavian artery (ARSA, arteria lusoria) is the most common intrathoracic vascular anomaly, affecting up to 2% of the population. However, aneurysms of congenital anomalies are extremely unusual and often present with dysphagia, dysphonia, or dyspnea due to compression of the surrounding structures. We report a case of an asymptomatic 57-year-old male with chronic kidney disease who was incidentally found to have a large aneurysm of the ARSA on preoperative computed tomography for laparoscopic nephrectomy. Surgery is unequivocally warranted as these aneurysms are associated with a high risk of complications, including thrombosis, embolism, and rupture. We debranched the ARSA, followed by anastomosis to the right carotid artery through a right neck incision. Subsequently, aneurysmal resection was performed through left thoracotomy. The patient had an uneventful postoperative recovery and was asymptomatic during the follow-up.

摘要

迷走右锁骨下动脉(ARSA,又称lusoria动脉)是最常见的胸内血管异常,影响高达2%的人群。然而,先天性异常的动脉瘤极为罕见,常因周围结构受压而出现吞咽困难、声音嘶哑或呼吸困难。我们报告一例57岁无症状男性慢性肾病患者,在术前腹腔镜肾切除术的计算机断层扫描中偶然发现患有巨大的ARSA动脉瘤。由于这些动脉瘤与包括血栓形成、栓塞和破裂在内的高并发症风险相关,明确需要进行手术。我们对ARSA进行了去分支,然后通过右颈部切口与右颈动脉进行吻合。随后,通过左胸切开术进行动脉瘤切除术。患者术后恢复顺利,随访期间无症状。

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