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• In early fetal life, the vitelline or omphalomesenteric duct that connects the
midgut to the yolk sac is normally obliterated by the 6th week. If the portion
connecting to the ileum fails to atrophy, a Meckel diverticulum results. This
congenital diverticulum arises from the antimesenteric margin of the intestine
and contains all layers of the normal bowel and is thus a true diverticulum. In
less than 25% of patients, a Meckel diverticulum also contains heterotopic
tissue of the stomach (and thus contains parietal cells that secrete hydrochloric
acid), pancreas, or both.
• Only about 2% of people with Meckel diverticulum develop complications.
Although diverticula are equally common among males and females, males are
2 to 3 times more likely to have complications.
• People can live their whole lives without ever
knowing they have a Meckel diverticulum, but
occasionally the abnormality causes
complications. Although diverticula are equally
common among boys and girls, boys are 2 to 3
Complications times more likely to have complications.
of Meckel Complications of Meckel diverticulum include
diverticulum • Bleeding
• Obstruction (blockage)
• Diverticulitis
• Perforation
• Tumors
Risk Factors for Meckel's Diverticulum
• Diverticulosis
• Angiodysplasia
• Hemorrhoids
• Crohn’s disease
• Ulcerative colitis
• Colon carcinoma
Treatment for Meckel's Diverticulum
• Surgery
• Surgery to remove the diverticulum will be required if bleeding develops. The
segment of small intestine that contains the diverticulum is removed. The ends of the
intestine are then sewn back together.
• Iron supplements to treat anemia are also prescribed and a blood transfusion if
bleeding was severe.
• If there is underlying infection or inflammation(peritonitis, ulcerative colitis,
diverticulitis):Control of the inflammation by using antibiotics(cefotxime)
(metro/clindamycin )and surgical excision of the diverticulum