Paediatric Respiratory Reviews
Volume 4, Issue 1 , Pages 74-78, March 2003

Isolated tracheo-oesophageal fistula

  • D.C.G Crabbe

      Affiliations

    • Corresponding Author InformationCorrespondence to: D. C. G. Crabbe. Tel.: +44-113-392-5077; Fax: +44-113-392-6609

Consultant Paediatric Surgeon, Department of Paediatric Surgery, Clarendon Wing, Leeds General Infirmary, Leeds LS2 9NS, UK

Abstract 

Congenital isolated tracheo-oesophageal fistula is a rare malformation that presents with a characteristic triad of symptoms: choking and cyanosis on feeding, recurrent lower respiratory tract infection and abdominal distension. Children are invariably symptomatic from birth, although the symptoms may be intermittent and may vary in severity. A high index of suspicion is required because the symptoms are not specific. Establishing the diagnosis can be difficult and neither radiology nor bronchoscopy is infallible. Surgical division of the fistula is curative.

Keywords:  tracheo-oesophageal fistula, bronchoscopy

 

PII: S1526-0542(02)00274-9

doi:10.1016/S1526-0542(02)00274-9

Paediatric Respiratory Reviews
Volume 4, Issue 1 , Pages 74-78, March 2003