| Literature DB >> 31984700 |
Giselle Cuestas1, Verónica Rodríguez2, Carolina Millán3, Patricio Bellia Munzón2, Gastón Bellia Munzón3.
Abstract
Congenital tracheoesophageal fistula not associated with esophageal atresia, known as H-type fistula, is an uncommon anomaly. It presents with cough, choking, and cyanosis during feeding and/or recurrent pneumonia. Although symptoms are usually present from birth, diagnosis is difficult. The rarity of this disease, non-specific symptoms, and the limitations of radiological and endoscopic confirmation of the fistula often result in a delay between presentation and diagnosis confirmation. Here we describe the clinical manifestations, assessment methods, and management of 3 newborn infants with H-type tracheoesophageal fistula, together with diagnosis recommendations to prevent unnecessary delays in the management of this condition. Sociedad Argentina de Pediatría.Entities:
Keywords: H-type tracheoesophageal fistula; bronchoscopy; newborn infant; thoracoscopy.
Mesh:
Year: 2020 PMID: 31984700 DOI: 10.5546/aap.2020.eng.56
Source DB: PubMed Journal: Arch Argent Pediatr ISSN: 0325-0075 Impact factor: 0.635