Meckel diverticulum (MD) is a congenital pouch on the antimesenteric border of the distal ileum.It is a remnant of the omphalomesenteric (vitelline) duct.These anomalies are seen all over the world with a fairly consistent prevalence of 0.2-4%.There is no strong evidence for genetic factors.There can be seen three possible variants: (1) an MD with the rest of the omphalomesenteric duct (OMD) seen as a terminal fibrous band connecting with the umbilicus; (2) the whole OMD remains patent; and (3) an umbilical cyst, a fluid-filled remnant in a part of the ductal pathway.The cause is unknown; no single gene mutation has been consistently associated with MDs, but new information is emerging about the pathogenesis of gut heterotopias.Some of these diverticula are seen in patients with trisomy 13, trisomy 18, trisomy 21, or with broader patterns of multiple congenital anomalies, including the Vertebral, Anal, Cardiac, tracheoesophageal, Renal, Limb anomalies (VACTERL) association.Meckel diverticulums can be associated with fibrous peritoneal bands, which can be associated with mechanical intestinal obstruction by kinking, compressing, or entrapping small bowel loops.Symptomatic cases may be diagnosed with a nuclear medicine technetium-99m pertechnetate Meckel scan that detects gastric tissue.Asymptomatic patients may be closely followed with conservative management.However, for symptomatic cases, a diverticulectomy is performed, and the fibrous bands or adhesions are released.If the base is broad, a segmental ileal resection is considered.
Atul Kumar Khare (Wed,) studied this question.