Meckel's diverticulum | |
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Schematic drawing of a Meckel's diverticulum with a part of the small intestine. | |
Classification and external resources | |
Specialty | medical genetics |
ICD-10 | C17.3, Q43.0 |
ICD-9-CM | 152.3, 751.0 |
OMIM | 155140 |
DiseasesDB | 7903 |
MedlinePlus | 000234 |
eMedicine | med/2797 ped/1389 rad/425 |
Patient UK | Meckel's diverticulum |
MeSH | D008467 |
A Meckel's diverticulum, a true congenital diverticulum, is a slight bulge in the small intestine present at birth and a vestigial remnant of the omphalomesenteric duct (also called the vitelline duct or yolk stalk). It is the most common malformation of the gastrointestinal tract and is present in approximately 2% of the population, with males more frequently experiencing symptoms.
Meckel's diverticulum was first explained by Fabricius Hildanus in the sixteenth century and later named after Johann Friedrich Meckel, who described the embryological origin of this type of diverticulum in 1809.
The majority of people with a Meckel's diverticulum are asymptomatic. An asymptomatic Meckel's diverticulum is called a silent Meckel's diverticulum. If symptoms do occur, they typically appear before the age of two years.
The most common presenting symptom is painless rectal bleeding such as melaena-like black offensive stools, followed by intestinal obstruction, volvulus and intussusception. Occasionally, Meckel's diverticulitis may present with all the features of acute appendicitis. Also, severe pain in the epigastric region is experienced by the patient along with bloating in the epigastric and umbilical regions. At times, the symptoms are so painful that they may cause sleepless nights with acute pain felt in the foregut region, specifically in the epigastric and umbilical regions.