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.