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Wireless Capsule Endoscopy Detects Meckel's Diverticulum in a Child with Unexplained Intestinal Blood Loss
I Xinias1, A Mavroudi, M Fotoulaki
1Third Pediatric Department and Pediatric Surgery Clinic, Hippocration Hospital, Thessaloniki, Greece.
Case Reports in Gastroenterology
|November 10, 2012
Summary
Meckel's diverticulum, a common congenital anomaly, can cause difficult-to-diagnose gastrointestinal bleeding. Wireless capsule endoscopy proved crucial in identifying the source of bleeding when other methods failed.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Diagnostic Imaging
Background:
- Meckel's diverticulum (MD) is the most common congenital anomaly of the gastrointestinal tract, affecting approximately 2% of the population.
- While often asymptomatic, symptomatic MD can present diagnostic challenges, particularly in pediatric patients.
- Gastrointestinal bleeding is a potential complication of Meckel's diverticulum.
Observation:
- An 8-year-old boy presented with recurrent episodes of significant gastrointestinal bleeding.
- Initial diagnostic evaluations, including GI scintigraphy and colonoscopy, were negative for the source of bleeding.
- Despite normal findings on upper endoscopy and colonoscopy during a second bleeding episode, further investigation was warranted.
Findings:
- Radiolabeling of blood constituents with (99m)Tc indicated a potential lesion in the ileocecal area.
- Wireless capsule endoscopy successfully identified a Meckel's diverticulum as the cause of the gastrointestinal bleeding.
- This case highlights the diagnostic difficulties associated with symptomatic Meckel's diverticulum.
Implications:
- Wireless capsule endoscopy should be considered in cases of obscure gastrointestinal bleeding, especially when conventional endoscopic methods are inconclusive.
- Early and accurate diagnosis of Meckel's diverticulum is essential for appropriate management and to prevent complications.
- This case underscores the importance of advanced diagnostic tools in pediatric gastroenterology for identifying rare congenital anomalies.
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