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Meckel's diverticulum containing enterolith mimicking acute appendicitis
ZakaUllah Jan1, Nisar Ahmed1, Naila Aziz1
1Khyber Teaching Hospital, Peshawar, Pakistan.
Introduction:
Meckel's diverticulum is a vestige of the vitello-intestinal duct. It is one of the most common congenital abnormality of the GI tract.
Case Presentation:
We present a case of a male patient who presented with pain in the peri-umbilical region and in right iliac fossa. A clinical diagnosis of acute appendicitis was made, but, interestingly it turned out to be a Meckel's diverticulum having enterolith intraoperatively. The patient underwent wedge resection and the post-operative course was uneventful.
Conclusion:
Meckel's diverticulum containing enterolith is rare. This can mimick as acute appendicitis and the surgeon needs to be wary of this.
Insights
A rare case of Meckel's diverticulum with an enterolith mimicked acute appendicitis. Surgical resection was successful, highlighting the importance of considering this congenital anomaly in differential diagnoses.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Congenital Abnormalities
Background:
- Meckel's diverticulum is a common congenital abnormality of the gastrointestinal tract, representing a remnant of the vitello-intestinal duct.
- It is a well-known entity in pediatric surgery and gastroenterology.
Observation:
- A male patient presented with symptoms consistent with acute appendicitis, including peri-umbilical and right iliac fossa pain.
- Intraoperative findings revealed a Meckel's diverticulum containing an enterolith, which had been clinically misdiagnosed.
Findings:
- The presence of an enterolith within a Meckel's diverticulum is an uncommon occurrence.
- This specific case highlights the potential for Meckel's diverticulum to present atypically, mimicking more common surgical emergencies.
Implications:
- Surgeons must maintain a high index of suspicion for Meckel's diverticulum, especially when clinical presentation is suggestive of acute appendicitis.
- Accurate preoperative diagnosis and intraoperative awareness are crucial for effective management of such rare gastrointestinal anomalies.
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