Ventilation Challenges Involved in a Rare Congenital Abnormality Masquerading as Esophageal Atresia: A Case Report
A premature neonate diagnosed with esophageal atresia secondary to polyhydramnios presented for diaphragmatic hernia repair. Preanesthesia evaluation suggested esophageal atresia with tracheoesophageal fistula. The decision was made to proceed with surgery; however, we were confronted with difficulty ventilating our patient. A few hours postsurgery, subcutaneous emphysema was appreciated in the neck region of our patient. On otolaryngological investigation, a single cleft running from the mouth until the carina was discovered. This rare deformity was a type 4 laryngeal cleft. This report will discuss both how we succeeded in ventilating our patient, and it will encourage extra diligence in preanesthesia evaluation.
Authors
- Jalaa Hossein
- Naser Hawash
- Alex Brodsky (ORCID: https://orcid.org/0000-0003-2606-3299)
- S. Avraham (ORCID: https://orcid.org/0009-0002-8732-0615)
- Ohad Hochman (ORCID: https://orcid.org/0000-0001-7424-7610)
- Mostafa Somri (ORCID: https://orcid.org/0000-0002-3814-1402)
- Feras Somri
Institutions
- Technion – Israel Institute of Technology (IL)
- University of Chieti-Pescara (IT)
Publication Details
- Journal
- A&A Practice
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1213/xaa.0000000000001951
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00