专利乌拉丘斯与专利小肠道管道:罕见的同时发生
Shreyas Dudhani1, Keerthana Bachagala, Bijay Kumar Suman
1Department of Pediatric Surgery, AIIMS, Patna, Bihar, India.
African journal of paediatric surgery : AJPS
|September 24, 2024
概括
本案例报告详细介绍了一名患有两种罕见的带先天性异常的婴儿:一种专利的 urachus 和一种专利的 vitello- intestinal duct. 手术干预是成功的,突出了小心剖析在骨-骨区域的重要性.
科学领域:
- 儿科手术 儿科手术
- 发展生物学 发展生物学
- 遗传异常是一种先天性异常.
背景情况:
- 带异常是一种常见的先天性疾病.
- 同时发生多个带异常的情况很少见.
- 专利 urachus 和专利 vitello肠道带来了独特的诊断和手术挑战.
研究的目的:
- 报告一个罕见的病例,即婴儿的尿道和小肠道同时存在.
- 描述这些综合异常的诊断和手术管理.
- 为了强调这个解剖区域的关键外科考虑.
主要方法:
- 无效的囊回路图用于诊断专利 urachus.
- 诊断和管理的外科探索.
- 切除和解剖为专利小肠道管道.
- 鼻腔切除. 鼻腔切除. 鼻腔切除.
- 组织病理学检查以确认.
主要成果:
- 在婴儿身上发现了一个专利的 urachus 和一个专利的 vitellointestinal duct.
- 进行了成功的手术切除和小肠道的解剖切除和 urachus 的切除.
- 组织病理学证实,肠上皮层覆盖了小肠道残留物和纤维状 urachal 残留物.
- 在异常之间识别出腹-腹血管.
结论:
- 子的先天性异常,包括 patent urachus 和 patent vitellointestinal duct,可以同时存在.
- 及时诊断和手术干预对于有利的结果至关重要.
- 意识到腹 - 介质血管的解剖关系对于预防手术内出血至关重要.
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