Meckel's diverticulum is the most common congenital malformation of the gastrointestinal tract. It affects 2% of the general population.[1] A 11-month-old male child presented with complaints of passing a black tarry color stool for 3 days. Meckel's scan showed a focal area of abnormal tracer uptake in the lower abdomen, just above the urinary bladder [Figure 1]. On laparotomy, a Meckel's diverticulum was found on the mesenteric border, around 30 cm proximal to the ileocecal junction supplied by the vitelline artery at the apex [Figure 2]. Resection and anastomosis were done. The histopathology report revealed Meckel's diverticulum with heterotopic gastric tissue [Figure 3]. The mesenteric border location of Meckel's diverticulum is very rare, and it is more alarming because it may erode the mesentery and its vasculature during diverticulitis causing devastating complications.[2]Figure 1: Meckel's scan showing an increased flow and abnormal tracer uptake in lower abdominal region, just above the urinary bladder (black arrow)Figure 2: Intraoperative photograph showing Meckel's diverticulum on the mesenteric border (yellow arrow) and vitelline artery at the apex (black arrow)Figure 3: Higher magnification shows diverticulum lined by intestinal epithelium and sub epithelium containing gastric foveolar or oxyntic glands (H and E; ×200)Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the legal guardian has given his consent for images and other clinical information to be reported in the journal. The guardian understands that names and initials will not be published and due efforts will be made to conceal patient identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.
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