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一个小孩的先天双胞胎腹膜:一个案例报告
Maria Rogalidou1, Chrysa Georgokosta2, Palagia M Karas3
1Division of Gastroenterology and Hepatology, First Department of Paediatrics, National and Kapodistrian University of Athens, 'Agia Sophia' Children's Hospital, 115 27 Athens, Greece.
Reports (MDPI)
|December 24, 2025
概括
先天性十二指甲膜 (CDD) 是婴儿肠道阻塞的一个罕见原因. 早期诊断和及时的手术或内镜干预对于患病婴儿的成功结果至关重要.
科学领域:
- 儿科手术 儿科手术
- 胃肠病学 胃肠病学
- 遗传异常 是一种先天性异常.
背景情况:
- 先天性十二指甲膜 (CDD) 是一种罕见的疾病,导致婴儿十二指甲膜阻塞.
- 它经常表现为持续的吐和无法壮成长.
- 诊断包括像上肠道系列和胃镜等成像.
研究的目的:
- 为了在婴儿身上呈现先天性十二指甲膜隔膜病例.
- 突出诊断挑战和成功的管理.
主要方法:
- 一个17个月大的雌性婴儿的病例报告,未能壮成长和吐.
- 诊断工作包括上部肠道系列和胃镜.
- 通过隔膜切除的十二指管切除术进行手术管理.
主要成果:
- 图像检查证实了十二指甲膜膜,导致显著的阻塞.
- 胃镜检查显示了近乎完全的闭塞和胃排空障碍.
- 成功的手术切除导致了无事件的恢复.
结论:
- 在持续吐和体重增加较低的婴儿中,应考虑先天的十二指膜.
- 及时诊断和干预,手术或内镜是必不可少的.
- 早期治疗可以改善这种罕见的先天性异常的结果.
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