| Literature DB >> 8863248 |
B B Simpson1, D P Ryan, P K Donahoe, J J Schnitzer, S H Kim, D P Doody.
Abstract
Complete laryngotracheoesophageal clefts (types III and IV) are rare congenital anomalies that occur when the primitive foregut fails to separate into the tracheobronchial tree and the esophagus. This article summarizes a 10-year institutional experience with six infants who had type IV clefts, presents a modification of the authors' surgical approach, and identifies pitfalls in the management of these infants. Three of the six children are long-term survivors. The recognition of specific complicating issues leads to a standardized approach, which can result in successful repair and long-term survival.Entities:
Mesh:
Year: 1996 PMID: 8863248 DOI: 10.1016/s0022-3468(96)90101-3
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545