Introduction:
Meckel’s diverticulum (MD) is considered the most common gastrointestinal tract (GIT) congenital anomaly.1 MD can lead to many complications including bleeding, obstruction, inflammation and perforation. The bowel obstruction may occur through volvulus, intussusception or herniation.2 During adult life, intussusception is usually due to malignancy, polyp, stricture or rarely MD.3 Here we report a rare case of small bowel intussusception secondary to Meckel’s diverticulum in his fourth decade of life.