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Detection of bronchoesophageal fistula in an infant: a case report
Aika Shoo1, Frederick Lyimo2, Charles Komba3
1Department of Paediatrics and Child Health, Muhimbili National Hospital, Dar es Salaam, Tanzania.
Insights
Bronchoesophageal fistula (BEF), a rare congenital condition, caused chronic respiratory issues in an infant. Surgical intervention was necessary after misdiagnosis as recurrent pneumonia, underscoring the need for high diagnostic suspicion.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Respiratory Medicine
Background:
- Bronchoesophageal fistula (BEF) is a rare congenital or acquired abnormal communication between the bronchus and esophagus.
- Infants with BEF may present with chronic cough and breathing difficulties, often misdiagnosed.
Abstract:
Bronchoesophageal fistula (BEF) is a rare malformation, presenting with abnormal communication between the bronchus and the esophagus, which can be either congenital or acquired. Congenital bronchoesophageal fistula is rare; this case study presents a clinical case of a six-month-old male infant of African descent with a history of chronic cough and breathing difficulties since birth, treated as a case of recurrent pneumonia without improvement. Following a thorough series of investigations, the diagnosis of bronchoesophageal fistula (BEF) was confirmed, prompting the decision to proceed with surgical intervention. This case highlights the importance of maintaining a high index of suspicion to accurately diagnose BEF.
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