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Double-barrel adult congenital broncho-esophageal fistulae-images
Prakash Joseph1, Birla Roy Gnanamuthu1, Negine Paul1
1Christian Medical College & Hospital, Vellore, India.
Insights
Congenital broncho-oesophageal fistulae (CBEF) are rare foregut anomalies. This report details a unique case of a double CBEF in an adult, highlighting its uncommon presentation and management.
Area of Science:
- Medical Science
- Embryology
- Surgical Science
Background:
- Congenital broncho-oesophageal fistulae (CBEF) are rare foregut developmental anomalies.
- These anomalies arise from abnormal embryonic development, specifically the persistent connection between the tracheal bud and foregut.
- Typically, CBEF manifest in early life with recurrent respiratory infections and failure to thrive.
Purpose of the Study:
- To report a rare case of congenital double barrel broncho-oesophageal fistula.
- To highlight the unusual presentation of this anomaly in a middle-aged adult.
- To emphasize the rarity of double CBEF, with only one prior reported case.
Main Methods:
- Case presentation of a middle-aged female patient.
- Review of relevant medical literature on congenital broncho-oesophageal fistulae.
- Surgical intervention involving fistula division and repair.
Main Results:
- A congenital double barrel broncho-oesophageal fistula was identified in a middle-aged adult.
- This represents an exceptionally rare occurrence, with limited precedent in medical literature.
- The patient's condition required definitive surgical management.
Conclusions:
- Congenital double barrel broncho-oesophageal fistulae are exceedingly rare, particularly in adults.
- Early diagnosis and surgical intervention are crucial for effective management.
- This case underscores the importance of considering rare congenital anomalies even in adult patients.
Abstract:
Congenital broncho-oesophageal fistulae (CBEF) are foregut developmental anomalies. They are formed due to the persistent attachment between the developing tracheal bud and the foregut in the embryo. They commonly present in young age and patients present with symptoms of recurrent respiratory tract infections and low body weight. Only one case of a double CBEF has been reported in literature so far. Here we present a congenital double barrel broncho-oesophageal fistula in a middle aged lady, which is a rare presentation. Definitive treatment involves division and repair of the fistula along with resection of the damaged portion of lung in select cases. We publish these images due to the rarity of a double fistula.
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