Beydoun Serina, Davis James W, Al-Ansari Namir
Department of Pediatric Gastroenterology, Children's Hospital of Michigan, Detroit, MI.
Central Michigan University College of Medicine, Detroit, MI.
ACG Case Rep J. 2025 Mar 5;12(3):e01640. doi: 10.14309/crj.0000000000001640. eCollection 2025 Mar.
Enteric duplication cysts are rare congenital anomalies that can present with nonspecific symptoms, making diagnosis difficult. We present a case of a 13-month-old woman with hematochezia, initially diagnosed with viral gastroenteritis, who was later found to have a cecal duplication cyst on imaging. Surgical resection with ileocecectomy was performed, and pathology confirmed the diagnosis of cecal duplication cyst. Early diagnosis and a multidisciplinary approach are essential for preventing complications such as bowel obstruction and perforation, ensuring optimal outcomes.
肠重复囊肿是罕见的先天性异常，可表现为非特异性症状，导致诊断困难。我们报告一例13个月大的女性，有便血症状，最初被诊断为病毒性肠胃炎，后来影像学检查发现其患有盲肠重复囊肿。实施了回盲部切除术进行手术切除，病理检查确诊为盲肠重复囊肿。早期诊断和多学科方法对于预防肠梗阻和穿孔等并发症、确保最佳治疗效果至关重要。
