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Title: Current management of laryngeal and laryngotracheoesophageal clefts. Author: DuBois JJ, Pokorny WJ, Harberg FJ, Smith RJ. Journal: J Pediatr Surg; 1990 Aug; 25(8):855-60. PubMed ID: 2401940. Abstract: Laryngeal and laryngotracheoesophageal clefts (L-LTEC) are uncommon anomalies in neonates that cause significant morbidity secondary to aspiration, pneumonia, and respiratory distress. Other anomalies of development, such as esophageal atresia and tracheoesophageal fistula (EA-TEF), are observed in 20% of patients with L-LTEC and often confuse the radiographic and clinical picture. Repair of L-LTEC depends on the length and location of the cleft, associated anomalies, and concurrent systemic illness. For type I L-LTEC, endoscopic repair occasionally is possible with microsurgical instrumentation. With types II to IV L-LTEC, an open approach must be used. Tracheotomy is a universal requirement, often for extended periods of time. Reported here is our experience with four cases of L-LTEC managed over the past 7 years at Texas Children's Hospital.[Abstract] [Full Text] [Related] [New Search]