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主动脉弓不完全血管环致成人吞咽困难 1 例报告。

Incomplete vascular ring of the aortic arch presenting with dysphagia in an adult: case report.

机构信息

Division of Cardiothoracic Surgery, National Cardiothoracic Centre of Excellence, University of Nigeria Teaching Hospital, Ituku/Ozalla, Enugu, Nigeria.

Department of Radiation Medicine, University of Nigeria Teaching Hospital, Ituku/Ozalla, Enugu, Nigeria.

出版信息

Pan Afr Med J. 2023 Aug 25;45:183. doi: 10.11604/pamj.2023.45.183.38569. eCollection 2023.

Abstract

Anomalies of the arterial branches of the arch of the aorta are rare, with the aberrant right subclavian artery being the most common of this anomaly. Majority of the anomalies are asymptomatic and often discovered as incidental findings. In the great majority of the symptomatic cases, the presentation may be either with breathlessness or dysphagia or both. This is in addition to the nature of the intrinsic arterial disease of the aberrant vessel, especially in adult patients; and unless borne in mind, the diagnosis is often missed leading to delays and wrong treatment. In this report we present a case of dysphagia in an adult male Nigerian initially diagnosed as œsophageal stricture from herbal potion ingestion but review of his imaging investigations gave a final diagnosis of dysphagia lusoria from an aberrant right subclavian artery. The difficulty in making a diagnosis and the need for a multidisciplinary review of the imaging investigations are highlighted. The patient was successfully treated by a combined trans-thoracic and cervical approach with division and re-implantation of the aberrant vessel unto the right common carotid artery. He has remained symptom-free for 2 years after surgery. Although the great majority of these anomalies are often asymptomatic, it is important they are borne in mind both in imaging investigations as well as in procedures involving structures in the upper visceral mediastinum. Various surgical approaches have been documented in the management of symptomatic ones; it is however recommended that options that ensure revascularization of the affected limb be selected.

摘要

主动脉弓动脉分支异常罕见,其中以迷走右锁骨下动脉最为常见。大多数异常是无症状的,通常作为偶然发现。在绝大多数有症状的病例中,表现可能是呼吸困难或吞咽困难,或两者兼有。这除了异常血管的固有动脉疾病的性质外,特别是在成年患者中;如果不加以注意,诊断往往会被遗漏,导致延误和错误的治疗。在本报告中,我们介绍了一名尼日利亚成年男性吞咽困难的病例,最初被诊断为草药摄入引起的食管狭窄,但对其影像学检查的回顾性诊断为迷走右锁骨下动脉引起的吞咽困难 Lusoria。强调了诊断困难和需要对影像学检查进行多学科审查的必要性。通过经胸和颈联合入路,对异常血管进行分割和再植入右颈总动脉,成功治疗了该患者。手术后 2 年,他一直无症状。虽然大多数这些异常通常是无症状的,但在涉及上内脏纵隔结构的影像学检查和程序中,都应牢记这些异常。在有症状的异常处理中已经记录了各种手术方法;然而,建议选择可确保受累肢体再血管化的方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d29/10656587/7ccebc05c589/PAMJ-45-183-g001.jpg

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