Aberrant Right Subclavian Artery-Induced Esophageal Stenosis Successfully Treated with Vascular Reconstruction: A Pediatric Case Report.

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2025-01-01 Epub Date: 2025-09-25 DOI:10.70352/scrj.cr.25-0182
Wataru Sumida, Kazuya Nagayabu, Kazuki Ota, Yuki Imai, Yasuyuki Ono, Hiroomi Murayama
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Abstract

Introduction: Aberrant right subclavian artery (ARSA) is the most common congenital anomaly of the subclavian artery, occurring in 0.2%-1.5% of the population. While typically asymptomatic, ARSA can cause dysphagia in older patients due to esophageal compression. In pediatric cases, it is less frequent and usually presents with chronic respiratory symptoms resulting from tracheal compression. Acute respiratory failure as a presentation of ARSA is extremely rare. This case report describes a pediatric patient with ARSA-associated esophageal stricture, leading to severe respiratory distress following food intake and requiring surgical treatment.

Case presentation: A 1.8-year-old girl developed an inspiratory stridor after eating. Initial inhalation therapy provided temporary relief, but persistent respiratory distress prompted further evaluation. CT revealed an esophageal foreign body, which was successfully extracted using a balloon catheter. However, continued respiratory distress necessitated intubation and intensive care. Bronchoscopy and enhanced CT confirmed tracheal compression due to ARSA, along with esophageal stenosis. Despite initial medical management, recurrent respiratory distress and feeding difficulties required surgical intervention. A right thoracotomy was performed to reposition the aberrant artery anterior to the trachea, alleviating the vascular compression. Postoperatively, the patient made a full recovery, resumed a normal diet, and remained symptom-free at the 6-month follow-up.

Conclusions: Symptomatic ARSA is rare in pediatric patients but can cause severe respiratory distress due to esophageal and tracheal compression. In cases of recurrent or severe symptoms, surgical intervention is essential to prevent life-threatening complications. This case highlights the importance of considering ARSA in pediatric patients with unexplained respiratory distress, especially when associated with feeding difficulties.

血管重建成功治疗右侧锁骨下动脉引起的食管狭窄1例儿科病例报告。
右锁骨下动脉异常(ARSA)是最常见的先天性锁骨下动脉异常,发生率为0.2%-1.5%。虽然ARSA通常无症状,但由于食管压迫,老年患者可引起吞咽困难。在儿科病例中,它不太常见,通常表现为由气管压迫引起的慢性呼吸道症状。急性呼吸衰竭作为ARSA的表现是极其罕见的。本病例报告描述了一位患有arsa相关食管狭窄的儿科患者,在进食后导致严重的呼吸窘迫,需要手术治疗。病例介绍:一名1.8岁女孩进食后出现吸气性喘鸣。最初的吸入治疗提供了暂时的缓解,但持续的呼吸窘迫促使进一步的评估。CT示食道异物,经球囊导管成功取出。然而,持续的呼吸窘迫需要插管和重症监护。支气管镜及增强CT证实ARSA所致气管受压,伴食管狭窄。尽管最初进行了医疗处理,但反复出现呼吸窘迫和进食困难需要手术干预。右开胸将异常动脉重新定位于气管前方,减轻血管压迫。术后患者完全恢复,饮食正常,随访6个月无症状。结论:有症状的ARSA在儿科患者中很少见,但由于食管和气管压迫可引起严重的呼吸窘迫。在复发或症状严重的情况下,手术干预是必不可少的,以防止危及生命的并发症。本病例强调了在患有不明原因呼吸窘迫的儿科患者中考虑ARSA的重要性,特别是当与喂养困难相关时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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