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Meckel diverticulum

Last updated: February 3, 2025

Summarytoggle arrow icon

A Meckel diverticulum is the most common congenital anomaly of the gastrointestinal (GI) tract and is caused by an incomplete obliteration of the vitelline duct. It is commonly approx. 5 cm (2 inches) long and located 60 cm (2 feet) proximal to the ileocecal valve. The diverticulum may contain native ileal mucosa or heterotopic (most commonly gastric) mucosa. Meckel diverticula are often asymptomatic and detected incidentally on imaging or during abdominal surgery. A symptomatic Meckel diverticulum usually causes painless lower GI bleeding in children < 2 years. Patients may also present with complications from a Meckel diverticulum including diverticulitis, bowel obstruction, and, rarely, peritonitis due to Meckel diverticulum perforation. Meckel diverticulum should be considered in patients with lower GI bleeding and inconclusive findings on initial workup. Diagnostic studies for Meckel diverticulum include Meckel scan, endoscopy, and laparoscopy. A symptomatic Meckel diverticulum is treated with surgical resection. For an asymptomatic Meckel diverticulum detected incidentally during abdominal surgery, resection is indicated in children and may be considered in adults. An asymptomatic Meckel diverticulum detected incidentally on imaging does not require treatment.

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Epidemiologytoggle arrow icon

Epidemiological data refers to the US, unless otherwise specified.

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Pathophysiologytoggle arrow icon

Embryology

  • The omphalomesenteric duct (vitelline or vitellointestinal) is a patent tubular structure connecting the yolk sac to the alimentary tract in the embryo.
  • The duct is normally obliterated by the 6–7th week of intrauterine life. [2]
  • Incomplete obliteration of the omphalomesenteric duct → persistence of the proximal (intestinal) segment of the duct → Meckel diverticulum

Meckel diverticulum

The rule of two's describes common features of Meckel diverticula: occurs in 2% of the population, 2% are symptomatic, mostly in children < 2 years, affects males twice as often as females, is located 2 feet proximal to the ileocecal valve, is ≤ 2 inches long, and can have 2 types of mucosal lining.

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Clinical featurestoggle arrow icon

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Diagnosistoggle arrow icon

Approach [1][6][7]

Meckel scan [7][8]

  • Description: a noninvasive nuclear medicine imaging technique using technetium-99m pertechnetate, which is preferentially absorbed by the gastric mucosa
  • Indications
    • Suspected Meckel diverticulum without active bleeding
    • Occult bleeding with unclear etiology
  • Findings: visualization of ectopic gastric mucosa lining the diverticulum [8]

Other imaging studies [1][7][9]

Routine imaging has low sensitivity and specificity for Meckel diverticula and is typically used to assess complications.

Endoscopy [7]

  • Double-balloon enteroscopy: an enteroscopic technique to visualize the entire small intestine
    • A long endoscope is advanced into the small intestine through the mouth or rectum.
    • Sequentially inflating and deflating two balloons advances the scope into the intestine by pleating the bowel over the scope.
  • Capsule endoscopy: allows for direct visualization of the diverticulum, but may fail to detect the diverticulum if the capsule passes the diverticular opening without recording it
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Differential diagnosestoggle arrow icon

The differential diagnoses listed here are not exhaustive.

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Managementtoggle arrow icon

All symptomatic diverticula require surgery. Managing asymptomatic diverticula is more nuanced and involves weighing the risk of future complications against surgical risks.

Management of symptomatic diverticula [6]

Management of asymptomatic diverticula [8][10][11]

  • Detected on imaging: no treatment necessary
  • Incidental finding during unrelated surgery
    • Children: resection typically indicated
    • Adults: individualized decision

Surgery [8][11]

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Complicationstoggle arrow icon

We list the most important complications. The selection is not exhaustive.

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