Your new experience awaits. Try the new design now and help us make it even better

CASE REPORT article

Front. Surg.

Sec. Pediatric Surgery

Volume 12 - 2025 | doi: 10.3389/fsurg.2025.1629836

Cystic Intestinal Duplication-Induced Secondary Intussusception with associated Incidental Meckel's Diverticulum in an Infant: A Case Report with Literature Review

Provisionally accepted
Chuanyang  LiuChuanyang Liu1,2Meng  ShiMeng Shi1,2Jinhua  JiaJinhua Jia1,2Yuexia  BaiYuexia Bai1,2Shengwei  LuanShengwei Luan1,2Hongzhen  LiuHongzhen Liu1,2Meng  KongMeng Kong1,2*
  • 1Children’s Hospital Affiliated to Shandong University, jinan, China
  • 2Jinan Children’s Hospital, jinan, China

The final, formatted version of the article will be published soon.

Background:Secondary intussusception in children is associated primarily with organic intestinal pathologies. Intestinal duplication constitutes an uncommon lead point for such cases, while its cooccurrence with an incidentally discovered Meckel's diverticulum represents an exceptionally rare clinical scenario.This report describes an 8-month-old female infant who presented with secondary intussusception initially attributed to a cystic intestinal duplication, with Meckel ' s diverticulum discovered incidentally during surgical exploration.Case presentation : An 8-month-old female infant was admitted with recurrent vomiting, intermittent fever, and episodes of intense abdominal pain. Abdominal ultrasound revealed ileocolic intussusception and a cystic mass (3.5 cm × 3.0 cm × 3.0 cm) near the ileocecal junction. After unsuccessful air enema reduction, emergency surgery was performed. During the operation, intussusception was found to be caused by cystic intestinal duplication, which acted as the primary lead point.Notably, a separate Meckel's diverticulum (measuring 2.5 cm × 2.0 cm × 1.5 cm in diameter) was discovered incidentally 30 cm proximal to the ileocecal valve on the antimesenteric border of the ileum, demonstrating no pathological connection to the intussusception.Both lesions were surgically removed. Pathological examination confirmed a cystic intestinal duplication and a Meckel's diverticulum containing ectopic gastric tissue. The patient recovered well postoperatively and showed no recurrence of symptoms over a 30-month follow-up period.In pediatric patients with secondary intussusception caused by enteric duplication, meticulous intraoperative evaluation following successful reduction is critical to identify concurrent intestinal anomalies, including inverted Meckel's diverticulum-a potential lead point for secondary intussusception. This case highlights the incidental discovery of a coexisting Meckel's diverticulum, which was prophylactically excised despite lacking immediate pathological relevance. Systematic exploration combined with tailored resection strategies ensures definitive resolution of intussusception and long-term complication prevention in such rare dual-pathology presentations.

Keywords: intestinal duplication cyst, Meckel's diverticulum, Secondary intussusception, pediatric, Gastrointestinal malformation

Received: 16 May 2025; Accepted: 11 Jul 2025.

Copyright: © 2025 Liu, Shi, Jia, Bai, Luan, Liu and Kong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Meng Kong, Children’s Hospital Affiliated to Shandong University, jinan, China

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.