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诊断和治疗D型先天性食道缩症
Cuizhu Feng1,2, Long Li1, Yanxia Zhang1
1Department of Pediatric Surgery, Capital Institution of Pediatrics, Beijing, People's Republic of China.
Pediatric surgery international
|October 10, 2023
概括
D型食道缩症往往表现出模糊的症状,导致经常误诊为C型. 早期检测和适当的手术修复对于有利的结果至关重要,特别是在没有严重并发症的患者中.
科学领域:
- 儿科手术 儿科手术
- 遗传性缺陷 遗传性缺陷是一种先天性缺陷
- 胃肠道手术 胃肠道手术
背景情况:
- D型食道缩症 (EA),以近端和远端囊为特征,提出了诊断挑战.
- 它的罕见性和缺乏特定的临床表现有助于延迟或不正确的诊断.
研究的目的:
- 描述D型EA目前的临床实践和结果.
- 突出错误诊断对患者管理和重新手术率的影响.
主要方法:
- 在2017年1月至2022年5月期间接受治疗的10名D型EA患者的回顾性分析.
- 对诊断方法,手术方法 (胸腔镜和开放式) 和患者结果的审查.
主要成果:
- 70%的患者最初被误诊为C型EA.
- 新生儿修复涉及胸腔镜绑定和解,可变检测近道.
- 非新生儿修复使用胸部和宫两种方法.
- 十分之九的患者获得治愈;一个死亡归因于严重的先天性心脏病.
结论:
- 类型DEA需要高度的临床怀疑,因为非特异性症状.
- 错误诊断为C型EA是导致计划外的重新手术的一个重要因素.
- 没有严重相关异常的患者在适当的手术干预后表现出良好的预后.
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