食管闭锁伴气管食管瘘及下腔静脉中断1例报告。

IF 0.6 Q4 SURGERY
European Journal of Pediatric Surgery Reports Pub Date : 2024-11-18 eCollection Date: 2024-01-01 DOI:10.1055/a-2448-3530
Xiao Long Mu, Junqiu Wang
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引用次数: 0

摘要

食管闭锁(EA)合并气管食管瘘(TEF)是一种先天性异常,可以带来复杂的手术挑战,特别是当伴有罕见的血管疾病,如下腔静脉(IVC)中断时。奇静脉的分裂是TEF修复的常见部分,但在出现下腔静脉中断的情况下,这可能导致危及生命的并发症。我们报告的情况下,新生儿诊断为EA, TEF,并中断下腔静脉,成功地通过开胸治疗。本病例强调了产前和产后成像在TEF修复前诊断血管异常的重要性,确保了奇静脉的保存,以防止致命的后果。提高对这种罕见关联的认识对于优化手术计划和结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Repair of Esophageal Atresia with Tracheoesophageal Fistula and Interrupted Inferior Vena Cava: A Rare Case Report.

Esophageal atresia (EA) with tracheoesophageal fistula (TEF) is a congenital anomaly that can present complex surgical challenges, especially when accompanied by rare vascular conditions like an interrupted inferior vena cava (IVC). The division of the azygos vein is a common part of TEF repair, but in the presence of an interrupted IVC, this can lead to life-threatening complications. We report the case of a newborn diagnosed with EA, TEF, and interrupted IVC, successfully treated through thoracotomy. This case underscores the importance of prenatal and postnatal imaging to diagnose vascular anomalies prior to TEF repair, ensuring the preservation of the azygos vein to prevent fatal outcomes. Raising awareness of this rare association is crucial to optimizing surgical planning and outcomes.

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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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