Application of fibrobronchoscopy-guided aortic suspension in pediatric patients with bronchial compression resulting from repair of coarctation of the aorta: a case report.

IF 2 3区 医学 Q2 PEDIATRICS
Huayi Tan, Xinke Zou, Ke Gong, Yifeng Yang, Zhongshi Wu, Jijia Liu, Sijie Wu
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引用次数: 0

Abstract

Background: Coarctation of the aorta (CoA) is one of the more prevalent congenital heart diseases (CHD). The conventional treatment approach involves surgical correction of the coarctation. This procedure, however, can be associated with several complications, such as re-stenosis, aneurysm formation and pseudoaneurysm. One rare but significant complication is left bronchial compression, which may result from anterior displacement of the thoracic aorta or compression of the trachea by adherent tissue.

Case presentation: We present a case of a 7-month-old postoperative CoA patient who developed stenosis due to compression of the left main bronchus by the thoracic aorta. After comprehensive evaluation, we utilized a fiberoptic bronchoscope to accurately expose the site of aortic compression and subsequently performed bronchial release and aortic suspension procedures to alleviate the symptoms. The child demonstrated a satisfactory recovery following the surgical intervention. This successful case provides valuable insights for managing similar cases in the future.

Conclusions: Computing tomography (CT) airway reconstruction enables precise diagnosis of tracheal stenosis secondary to aortic arch pathology or coarctation repair. Intraoperative fiberoptic bronchoscopy provides real-time anatomical localization of stenotic segments, warranting standardization in high-risk aortic surgeries to ensure airway patency. Three-dimensional airway modeling should be incorporated into perioperative reassessment and longitudinal follow-up protocols.

纤维支气管镜引导下主动脉悬吊术在主动脉缩窄修复所致支气管受压患儿中的应用1例。
背景:主动脉缩窄(CoA)是较为常见的先天性心脏病(CHD)之一。传统的治疗方法包括手术矫正缩窄。然而,该手术可能伴随一些并发症,如再狭窄、动脉瘤形成和假性动脉瘤。一个罕见但重要的并发症是左支气管压迫,这可能是由胸主动脉前移位或气管被附着组织压迫引起的。病例介绍:我们报告一例7个月大的CoA术后患者,由于胸主动脉压迫左主支气管而发生狭窄。在全面评估后,我们使用纤维支气管镜准确暴露主动脉受压部位,随后进行支气管释放和主动脉悬吊手术以缓解症状。手术后患儿表现出满意的恢复。这个成功的案例为将来管理类似的案例提供了有价值的见解。结论:计算机断层扫描(CT)气道重建可以准确诊断主动脉弓病变继发气管狭窄或狭窄修复。术中纤维支气管镜提供狭窄段的实时解剖定位,保证高危主动脉手术的标准化,以确保气道通畅。三维气道建模应纳入围手术期再评估和纵向随访方案。
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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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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