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Enteric duplication cysts (EDCs) are rare congenital malformations that form during embryonic development of the gastrointestinal (GI) tract.Symptoms may include vomiting, abdominal distension, a palpable abdominal mass, or bleeding, but they can vary depending on the lesion's location.1 We present the case of a 9-year-old male with recurrent hematochezia and abnormal findings on small bowel capsule endoscopy (SBCE), ultimately diagnosed as an EDC on exploratory laparoscopy.
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Sarata et al. (2026) studied this question.
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