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Published on: August 23, 2022
Gastrointestinal Duplication Presenting as Neonatal Intestinal Obstruction: An Experience of 15 Years at Tertiary
Kamal Nain Rattan1, Shruti Bansal2, Aastha Dhamija2
1Department of Pediatric Surgery, Pt. B.D. Sharma PGIMS Rohtak, Haryana.
Insights
Gastrointestinal tract duplications are rare congenital anomalies in neonates, often causing intestinal obstruction. Early diagnosis and surgical management are crucial for successful outcomes in these infants.
Area of Science:
- Pediatric Surgery
- Congenital Anomalies
- Gastrointestinal Disorders
Background:
- Gastrointestinal tract (GIT) duplications are rare congenital anomalies, most commonly found in the small intestine.
- These duplications can manifest as abdominal masses or intestinal obstruction, necessitating surgical intervention, or remain asymptomatic.
- This study reports a 15-year experience with duplication cysts in neonates.
Purpose of the Study:
- To analyze the clinical presentation and management of gastrointestinal tract duplications in neonates.
- To evaluate surgical outcomes for neonates with these congenital anomalies.
- To highlight the importance of early diagnosis and intervention.
Main Methods:
- A retrospective study was conducted between 2001 and 2015 in a pediatric surgery department.
- Data from neonates diagnosed with GIT duplications were analyzed, including antenatal diagnosis, age, sex, clinical presentation, investigations, surgical management, and outcomes.
- Focus was on neonates with gastrointestinal duplications.
Main Results:
- Seventeen neonates were diagnosed with GIT duplications over 15 years, with a male-to-female ratio of 3.3:1.
- The ileum was the most frequent site (71%), followed by duodenum, stomach, colon, and cecum.
- Most neonates presented with sub-acute intestinal obstruction, successfully managed by resection and anastomosis; 4 cases had associated gut atresia, and 1 had gut perforation.
Conclusions:
- Gastrointestinal tract duplications in neonates typically present with symptoms of obstruction.
- Prompt diagnosis and surgical management are essential to minimize postoperative complications and mortality.
- Effective surgical strategies lead to successful outcomes in neonates with these anomalies.
Background:
Gastrointestinal tract (GIT) duplications are one of the rare congenital anomalies and can occur in any portion of the gastrointestinal tract but are more commonly encountered in small intestine. The duplication cysts cause symptoms like abdominal mass and intestinal obstruction requiring surgery or may remain asymptomatic. We are reporting our 15 years' experience duplication cysts presenting in neonates.
Methods:
It is a retrospective study undertaken in the department of pediatric surgery between 2001 and 2015 for GIT duplications in neonates. Patients were analyzed for their antenatal diagnosis, age, sex, clinical diagnosis, investigatory approach, operative management and surgical outcomes.
Results:
Total number of neonates, diagnosed with gastrointestinal duplication in the last 15 years, was 17. Male to female ratio was 3.3:1. The most common location was found to be the ileum occurring in 71% of cases. Apart from ileum, 2 cases of duodenal and 1 case each of gastric, colonic and cecal duplication cyst were encountered. Majority cases presented with sub-acute intestinal obstruction and were managed successfully by resection and end to end anastomosis. Associated gut atresia was found in 4 cases while 1 case was found to be associated with perforation of gut.
Conclusion:
Gastrointestinal tract duplications often present with typical symptoms of gastrointestinal tract obstruction. Early diagnosis and management is required to prevent postoperative morbidity and mortality.
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