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双大动脉门:一个病例系列和多学科的外科手术经验
Jad Abdul Khalek1, Karim Kanbar1, Bshara Sleem1
1Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
JACC. Case reports
|February 24, 2026
概括
双大动脉门 (DAA),一种罕见的血管异常,可以在晚年出现模糊的症状,延迟诊断. 早期识别和手术修复为受影响儿童提供了显著的症状缓解和改善的结果.
科学领域:
- 心血管外科心血管外科
- 儿童心脏病学 儿童心脏病学
- 遗传性心脏病是一种先天性心脏病.
背景情况:
- 双大动脉 (DAA) 是一种罕见的先天性异常,导致完整的血管环.
- 症状通常出现在婴儿期,但可能是微妙的,导致诊断延迟.
- 错误地归因于常见的呼吸道疾病是很常见的.
研究的目的:
- 突出DAA延迟呈现的可能性.
- 强调在患有持续呼吸道或胃肠道问题的儿童中考虑DAA的重要性.
- 审查DAA修复的手术结果.
主要方法:
- 病例系列报告了3名患有DAA的儿科患者的病例报告.
- 对临床表现,诊断成像和手术管理的审查.
- 对术后结果的评估.
主要成果:
- 由于非特异性表现,患者经历了长时间的症状和延迟诊断.
- 影像检测证实DAA与一个完整的血管环在所有情况下.
- 通过左胸切除术进行手术修复,导致显著的临床改善.
结论:
- 非特定的症状可能导致DAA的延迟诊断.
- 考虑在没有解释的呼吸或食困难的儿童中使用DAA.
- 手术正是安全的,有效的,并提供了大量的症状缓解与低发病率.
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