A previously healthy 11-year-old boy presented with an acute onset of hematochezia, right abdominal pain and syncope. On admission, he was found to be hypotensive with a blood pressure of 90/60 mmHg, and tachycardic with a pulse rate of 100 beats/min. The hemoglobin level was 8.1 g/dL. The boy was promptly resuscitated responding with a blood pressure of 110/70 mmHg, and a pulse rate of 80 beats/min. The physical examination was otherwise unremarkable. The abdomen was soft with no guarding or rebound tenderness. The rectal examination was unremarkable apart from traces of fresh blood. The platelet count of 307 9 10/L was normal, and he did not have a coagulopathy. Erect chest radiograph and abdominal radiograph studies were unremarkable with no evidence of pneumoperitoneum or other abnormality. An abdominal ultrasound scan was normal with no intussusception detected. A Meckel’s scan was performed to evaluate for a Meckel’s diverticulum containing ectopic gastric mucosa. After intravenous administration of 155 MBq (4.19 mCi) of Technetium pertechnetate, images of the abdomen were acquired with a dual-head gamma camera (ECAM, Siemens, Erlangen, Germany). The Meckel’s scan showed an abnormal focus of tracer activity in the right upper abdomen that appeared early with gastric activity, indicative of ectopic gastric mucosa (Fig. 1, arrow). The abnormal tracer was persistent and unchanged in position over 60 min, distinguishing it from physiological bowel activity. Despite the unusual location, a Meckel’s diverticulum containing ectopic gastric mucosa was thought probable. The boy underwent a laparoscopy. Intraoperatively, a 4 cm long inflamed Meckel’s diverticulum was found arising from the ileum, approximately 15 cm from the ileocecal junction, and this was located ‘‘ectopically’’ in the right hypochondrium (Fig. 2, arrow). Dark bluish colored blood from a recent hemorrhage was seen through the bowel wall (Fig. 2, arrowheads). The Meckel’s diverticulum was resected, and histology confirmed that the diverticulum contained the gastric mucosa. The patient recovered swiftly after the surgery. A Meckel’s diverticulum is the most common congenital abnormality of the gastrointestinal tract, and is found in 1–3% of the population [1]. It is a result of a failure of regression of the omphalomesenteric duct, and is frequently located within 100 cm proximal from the ileocecal valve, and hence, symptoms typically involved the lower abdomen [1]. It is most frequently asymptomatic, with symptoms being present in approximately 25% of the cases [2, 3]. The symptoms arise from the complications of a Meckel’s diverticulum, which include bleeding, intestinal obstruction, diverticulitis, vesicodiverticular fistula and tumor [2, 3]. Bleeding secondary to ectopic gastric mucosa is the most common complication of a Meckel’s diverticulum, and is most often seen in the pediatric population, particularly in patients younger than 2 years of age [3]. In adults, the most common complication of a Meckel’s diverticulum is intestinal obstruction, which may be secondary to intussusception, volvulus or internal herniation S.-J. Lu (&) A. Sinha Department of Diagnostic Imaging, National University Hospital, 5 Lower Kent Ridge Road, Singapore 119074, Singapore e-mail: suat_jin_lu@yahoo.com
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