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"Unveiling the uncommon: Fibrous band of Meckel's diverticulum and acute appendicitis in a single case"
Urooj Fatima1, Muhammad Shair Ismail1, Ahmad Ismail2
1Faisalabad Medical University Faisalabad, Pakistan.
Introduction:
Meckel's diverticulum (MD) is a congenital anomaly of the gastrointestinal tract that occurs in approximately 2% of the population. While often asymptomatic, it can present with complications such as gastrointestinal bleeding, inflammation, or intestinal obstruction. The coexistence of MD with acute appendicitis is exceedingly rare and poses significant diagnostic and therapeutic challenges.
Case Presentation:
We report the case of a 15-year-old male who presented with severe abdominal pain, nausea, vomiting, constipation, and fever. Clinical examination revealed a distended and tender abdomen with marked paraumbilical and right iliac fossa tenderness. Imaging studies indicated features of intestinal obstruction. During exploratory laparotomy, a Meckel's diverticulum tethered to the umbilicus by a fibrous band was identified, with the ileum twisted around the band causing an obstruction. Additionally, acute appendicitis with pelvic pus was discovered. Surgical management involved division of the fibrous band, wedge resection of the Meckel's diverticulum, and appendectomy. The patient had an uneventful recovery and was discharged on the fifth postoperative day.
Discussion:
This case highlights the rare presentation of concurrent Meckel's diverticulum-associated small bowel obstruction and acute appendicitis. It underscores the importance of maintaining a high index of suspicion for multiple abdominal pathologies in patients presenting with acute abdomen. Prompt diagnosis and surgical intervention are critical to achieving favorable outcomes in such complex cases.
Conclusion:
This case emphasizes the diagnostic and management challenges of concurrent abdominal pathologies and provides valuable insights into the surgical approach for such rare clinical scenarios.
Insights
This case report details a rare instance of a 15-year-old male with Meckel's diverticulum (MD) causing small bowel obstruction and concurrent acute appendicitis. Prompt surgical intervention led to a full recovery, highlighting the need for vigilance in complex abdominal cases.
Area of Science:
- Gastroenterology
- Surgical Case Reports
- Pediatric Surgery
Background:
- Meckel's diverticulum (MD) is a congenital anomaly affecting ~2% of the population.
- MD can cause complications like obstruction, bleeding, or inflammation.
- Concurrent MD and acute appendicitis is exceptionally rare, presenting diagnostic and therapeutic challenges.
Observation:
- A 15-year-old male presented with symptoms of intestinal obstruction and fever.
- Clinical and imaging findings suggested obstruction.
- Exploratory laparotomy revealed MD causing obstruction via a fibrous band and coexisting acute appendicitis with pelvic pus.
Findings:
- The patient underwent surgical correction, including division of the fibrous band, MD resection, and appendectomy.
- The surgical management successfully resolved both Meckel's diverticulum-associated small bowel obstruction and acute appendicitis.
- The patient experienced an uneventful recovery and was discharged on postoperative day five.
Implications:
- This case underscores the importance of considering multiple abdominal pathologies in acute abdomen presentations.
- High index of suspicion is crucial for diagnosing rare concurrent conditions like MD with appendicitis.
- Prompt diagnosis and surgical intervention are vital for favorable outcomes in complex pediatric surgical cases.
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