A
Meckel diverticulum is a congenital, blind pouch on the
antimesenteric border of the distal ileum, caused by incomplete obliteration of the embryonic
vitelline (omphalomesenteric) duct. It is a
true diverticulum, meaning it contains mucosa, muscularis, and serosa.
Merck Manual overview
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Present in about 2% of people
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Approximately 2 feet proximal to the ileocecal valve
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Roughly 2 inches long
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Male:female ratio about 2:1
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Often symptomatic before age 2 years
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Only about 4% become symptomatic
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Robbins, Cotran & Kumar Pathologic Basis of Disease, p. 726
Most people remain asymptomatic. Complications include:
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Painless lower gastrointestinal bleeding
- Typical in children
- Maroon or dark red stool, sometimes melena
- Usually from acid-related ileal ulceration adjacent to ectopic gastric mucosa.
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Intestinal obstruction
- Volvulus around a fibrous vitelline band
- Intussusception, with the diverticulum as a lead point
- Internal herniation or entrapment by a mesodiverticular band
- May present with colicky pain, vomiting, and distension.
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Diverticulitis or perforation
- Mimics acute appendicitis: right lower quadrant pain, fever, and tenderness.
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Littre hernia
- A Meckel diverticulum within an inguinal or femoral hernia sac.
Recent reviews found in PubMed focus on specialized diagnostic scenarios, including capsule-endoscopic diagnosis and rare torsion presentations. They do not change the standard clinical framework above (PMIDs: 40202427, 40696289).