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带有双边面部裂的气管食道:一种罕见的情况
Nitin James Peters1, Shaswati Behera1, Ramyasree Bade1
1Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Journal of Indian Association of Pediatric Surgeons
|June 30, 2023
概括
本病例报告详细介绍了一种罕见的食道缩和气管-食道带与双边面部裂 (巨) 的关联. 婴儿是一个婴儿.
科学领域:
- 面外科手术 面外科手术
- 儿科外科手术 儿科外科手术
- 有先天性异常.
背景情况:
- 面部部或侧面裂 (巨),Tessier数目7,是一种罕见的先天性异常.
- 这些裂往往呈现出第一和第二枝状 derivatives 的变形,影响口腔美学和功能.
- 双边横断裂是不常见的,它们与气管食道 (TEF) 的关联是前所未有的.
研究的目的:
- 报告一个独特的食道缩症 (EA) 和TEF同时发生的病例.
- 突出管理涉及面和食道结构的复杂先天性异常所面临的挑战.
- 为了对罕见的裂呈现的文献做出贡献.
主要方法:
- 一个新生儿被诊断患有食道缩,TEF和双边面部裂 (巨) 的病例介绍.
- 进行了食道动的手术修复.
- 临床随访,以评估患者手术后的状况.
主要成果:
- 患者成功地修复了食道缩症,在充分食后就出院了.
- 婴儿继续呈现巨,等待手术纠正.
- 之前没有任何报告详细说明EA,TEF和宏观的同时发生.
结论:
- 食道缩,TEF和宏的共存代表了一个极其罕见的先天性表现.
- 在这种情况下,EA的成功管理允许专注于随后的面重建.
- 需要进一步的研究和病例报告,以了解这种复杂病例的胚胎学基础和最佳管理策略.
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