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伴有双侧面部裂隙的气管食管瘘:一种罕见情况。

Tracheoesophageal Fistula with Bilateral Facial Cleft: A Rare Occurrence.

作者信息

Peters Nitin James, Behera Shaswati, Bade Ramyasree, Dogra Shivani, Solanki Shailesh, Samujh Ram

机构信息

Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

J Indian Assoc Pediatr Surg. 2023 May-Jun;28(3):260-262. doi: 10.4103/jiaps.jiaps_171_22. Epub 2023 May 2.

Abstract

Commissural or lateral facial cleft (macrosomia), classified at Tessier number 7 craniofacial clefts, is a rare congenital anomaly usually associated with deformities of other structures developed from the first and second branchial arches. It affects the esthetics and functional aspect of the oral cavity. Bilateral transverse cleft occurring alone is uncommon and it's with tracheoesophageal fistula (TEF) has not been reported to the best of our knowledge. We report a case of esophageal atresia (EA) and TEF with macrosomia. EA was repaired, and the patient was discharged on full feeds. He is awaiting cleft repair.

摘要

连合性或侧面面部裂(巨口症),归类于第7号Tessier颅面裂,是一种罕见的先天性异常,通常与由第一和第二鳃弓发育而来的其他结构畸形相关。它影响口腔的美观和功能。单独发生的双侧横向裂并不常见,据我们所知,伴有气管食管瘘(TEF)的情况尚未见报道。我们报告一例患有巨口症的食管闭锁(EA)和TEF病例。EA已修复,患者全量喂养后出院。他正在等待腭裂修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aad/10305959/21c5d534ef4f/JIAPS-28-260-g001.jpg

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