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Prenatally Diagnosed Multiple Enteric Duplication Cysts in an Infant: A Rare Case and Surgical Approach
Elisavet Kanna1, Zoi Lamprinou1, Jonida Mene2
1Pediatric Surgery, Panagiotis and Aglaia Kyriakou Children's Hospital, Athens, GRC.
Insights
Multiple enteric duplication cysts (EDCs), rare congenital anomalies, were diagnosed prenatally in an infant. Surgical resection was successful, highlighting the importance of early detection and intervention for these gastrointestinal malformations.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Gastroenterology
Background:
- Enteric duplication cysts (EDCs) are uncommon congenital anomalies of the gastrointestinal tract.
- Multiple EDCs are exceptionally rare, presenting unique diagnostic and management challenges.
Abstract:
Enteric duplication cysts (EDCs) are rare congenital anomalies that can occur along any part of the gastrointestinal tract, with multiple cysts being exceptionally uncommon. We present the case of a five-month-old infant with multiple prenatally diagnosed EDCs, including a pedunculated cyst and a large tubular duplication near the ileocecal valve. The infant remained asymptomatic, and elective surgical resection was performed. Histopathology confirmed the diagnosis, revealing distinct structural features and chronic inflammatory changes. This case highlights the morphological variety of multiple duplication cysts and underscores the importance of prenatal detection and timely surgical intervention to prevent complications.
