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Published on: October 29, 2014
Forshal type IE appendiceal intussusception: A case report
Aramva Bikram Adhikari1, Kshitiz Acharya1, Karishma Kathayat2
1Maharajgunj Medical Campus, Tribhuvan University, Institute of Medicine, Maharajgunj, Nepal.
Insights
Appendiceal intussusception is a rare condition often diagnosed during surgery. Appendectomy is the recommended treatment for this unusual cause of abdominal pain in children.
Area of Science:
- Pediatric Surgery
- Gastroenterology
Background:
- Appendiceal intussusception is a rare cause of abdominal pathology.
- Clinical presentation is often non-specific, mimicking other abdominal conditions.
- Preoperative diagnosis is challenging due to vague symptoms.
Purpose of the Study:
- To report a case of appendiceal intussusception in a child.
- To highlight diagnostic challenges and management strategies.
Main Methods:
- Case report of a 5-year-old boy presenting with abdominal pain and vomiting.
- Initial diagnosis of ileocolic intussusception.
- Failed hydrostatic reduction, followed by laparotomy and appendectomy.
Main Results:
- Intraoperative findings revealed complete intussusception of the appendix.
- Appendectomy was successfully performed.
- The postoperative period was uneventful.
Conclusions:
- Appendiceal intussusception is typically diagnosed intraoperatively.
- Appendectomy is the treatment of choice.
- Awareness among radiologists and pediatric surgeons is crucial for recognizing this rare entity.
Introduction:
Appendiceal intussusception is a rare condition. Clinical features are not specific for it. Patients may present with abdominal pain and vomiting. These symptoms represent a variety of abdominal pathology. Preoperative diagnosis is difficult because of the non-specific clinical features. We present a case report of a child who initially presented with ileocolic intussusception.
Case Presentation:
This is a case report of a 5-years-old boy with abdominal pain and vomiting. He had an ileocolic intussusception 2 days back, and was successfully managed by hydrostatic reduction and discharged. On ultrasonography, an intussusception was identified in the ileocaecal region. Hydrostatic reduction failed this time and laparotomy was performed. On laparotomy, there was complete intussusception of the appendix with normal ileocaecal junction. Appendectomy was performed. Post-operative period was uneventful.
Discussion:
Appendiceal intussusceptions are mostly diagnosed intra-operatively. The clinical features may mimic various other acute and chronic abdominal conditions. Type IE appendiceal intussusception, as described by Forshal, is a rare condition. Appendectomy with a rim of the caecum is the procedure of choice.
Conclusion:
Though ileocaecal intussusceptions are common in children, appendiceal intussusceptions are rare and are usually diagnosed during the operative procedure. Radiologists and pediatric surgeons should be aware of this rare entity. Appendectomy is the treatment of choice in most of the appendiceal intussusceptions.
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