喘息和窒息--血管原因:病例报告

Keerthy Nath S, Mamatha Munaf, Jagadish A, Thomas Koshy, Saravana Babu
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摘要

双主动脉弓是一种极为罕见的血管畸形,可导致幼儿喘息发作和吞咽困难。根据气道受压的程度,麻醉处理方法各不相同。我们的患者是一名 10 个月大的男孩,反复发作喘息和窒息。气管和食道被双主动脉弓压迫,婴儿被送去进行非优势主动脉弓的手术分割。由于气道受压,麻醉管理通常比较困难。麻醉处理方法多种多样,包括在诱导过程中保持自主呼吸,根据气管尺寸仔细选择合适的气管导管,以及需要进行气管重建手术来处理气管狭窄。术中手术管理取决于从上下肢动脉压变化中识别出占优势的主动脉弓,并修复相关的心内缺损。我们报告了一个这样的病例,并取得了成功的结果。附三维计算机断层扫描图像,以便清楚了解解剖结构。血管环是导致儿童喘息和窒息发作的已知但罕见的原因,因此需要仔细规划麻醉以获得良好的效果。
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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Wheezing and Choking—A Vascular Cause: A Case Report

The double aortic arch is an extremely rare vascular malformation that can be a cause of wheezing episodes and dysphagia in a young child. Depending on the extent of airway compression, anaesthesia management varies. Our patient was a 10-month-old boy with recurrent wheezing and choking episodes. The trachea and oesophagus were compressed by the double aortic arch, and the baby was posted for surgical division of the non-dominant aortic arch. The anaesthesia management is often difficult owing to the airway compression. The anaesthesia management varies from maintaining spontaneous breathing during induction and careful selection of an appropriate endotracheal tube based on the tracheal dimensions to requiring tracheal reconstruction procedures to manage the tracheal stenosis. Intraoperative surgical management depends on the identification of the dominant aortic arch from arterial pressure changes of upper and lower limbs and the repair of associated intra-cardiac defects. We report one such case with a successful outcome. Three-dimensional computed tomography images are attached for a clear understanding of the anatomy. Vascular rings are known, but rare causes of wheezing and choking episodes in a child, which requires careful planning of anaesthesia for a good outcome.

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