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Concomitant intussusception and appendicitis "appendi-sception" in children: A case report and review of literature
Bhawesh Bhattarai1, Sujan Paudel2, Prajjwol Luitel2
1Department of General Surgery, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Nepal.
Insights
Concurrent appendicitis and intussusception, a rare pediatric condition, presents diagnostic challenges. Surgical intervention, including appendectomy, effectively treated this rare case of "appendi-sception".
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Diagnostic Imaging
Background:
- Intussusception is the primary cause of bowel obstruction in children under two.
- Concurrent intussusception and appendicitis ('appendi-sception') is exceptionally rare.
Observation:
- A 37-month-old boy presented with symptoms of intussusception, including abdominal pain, vomiting, and red currant jelly stool.
- Ultrasound confirmed intussusception; failed hydroreduction prompted surgical exploration.
- Laparotomy revealed ileocolic intussusception with an inflamed appendix.
Findings:
- Histopathology confirmed suppurative appendicitis.
- Appendectomy and manual reduction successfully treated the condition.
- The patient experienced an uneventful recovery and one-year follow-up.
Implications:
- Appendicitis as a lead point for intussusception is rare and difficult to diagnose preoperatively.
- Symptom overlap between intussusception and appendicitis complicates diagnosis.
- Failure of hydroreduction necessitates considering secondary causes like appendicitis, potentially warranting CT scans and appendectomy.
Introduction:
Pediatric intussusception is the leading cause of bowel obstruction in children under 2 years of age. Concurrent intussusception and appendicitis, known as "appendi-sception" is exceptionally rare in the pediatric population.
Case Presentation:
A 37-month-old boy presented with periumbilical abdominal pain, vomiting, and red currant jelly stool for two weeks. Clinical examination and ultrasonography confirmed intussusception. Hydroreduction was attempted twice but failed, necessitating surgical intervention. During exploratory laparotomy, ileocolic intussusception and an inflamed appendix were discovered for which an appendectomy was performed. The postoperative course was uneventful, and histopathology confirmed suppurative appendicitis. The patient had no difficulty at the one-year follow-up.
Discussion:
Intussusception with appendicitis as a lead point is rare and often challenging to diagnose preoperatively. The literature review revealed 11 pediatric cases, with concomitant intussusception and appendicitis highlighting diagnostic challenges due to symptom overlap. The overlap in symptoms between intussusception and appendicitis complicates diagnosis. Hydroreduction failure should prompt consideration of secondary causes, including appendicitis.
Conclusion:
Considering secondary causes in intussusception is crucial, especially when initial management fails. CT scans should be considered in such cases. Appendectomy and manual reduction can effectively manage concurrent intussusception and appendicitis. This case underscores the importance of considering multiple diagnoses in complex pediatric abdominal presentations.
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