A rare case presentation of combined enteric duplication cyst both tubular and cystic

Enteric duplication cyst are rare congenital malformations of children and can develop anywhere along the gastrointestinal (GI) tract being ileum most frequent location, they don’t communicate with GI lumen. They usually detected prenatally or in first years life. The size, type, mucosal pattern produces varied clinical presentation different imaging findings. Ultrasonography (USG) is commonly used method for diagnosis. A 4-year-old boy was admitted our hospital recurrent on off abdominal pain, getting USG he has diagnosed having tubular enteric both computed tomography (CT) scan. Surgery performed resection anastomosis done. Macroscopic histologic findings confirmed diagnosis arising from ileum. Although intestinal duplications considered to be benign lesions, may result significant morbidity mortality if left untreated.