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.

Insights

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.