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A case report of ectopic pancreatitis in an isolated enteric duplication cyst
BMC Surgeryvolume 19, Article number: 64 (2019)
Isolated enteric duplication cyst is an intestinal duplication cyst found in a distant location from the intestinal tract and it is said to have its own blood supply. Meckel’s diverticulm is considered as an antimesenteric structure and has its own blood supply. However, there are some reported cases of Meckele’s diverticum in the mesenteric side. Ectopic pancreas may be found in both entities.
A 5-year-old girl presented with increasing abdominal pain around the umbilicus. On laboratory investigation serum pancreatic enzymes and C-reactive protein were elevated. Abdominal computed tomography (CT) revealed a normal pancreas but a cystic lesion in the mesentery of the ileum. A nodule with a marked enhancement was observed in the wall of the lesion. During the laparoscopy, the lesion was found at the root of the mesentery and was distant from the ileum. The lesion was resected suspecting an abscess. Pathologically, the wall of the lesion consisted of small bowel like tissue, and pancreatic tissue was seen beneath the mucosa. There were some post inflammatory changes in the pancreatic tissue. Retrospectively on thin slice enhanced CT, an independent blood supply was noted. Based on these findings, a diagnosis of ectopic pancreatitis in an iliac intestinal duplication cyst was made.
Isolated enteric duplication cyst in the root of ileal mesentery and mesenteric Meckel’s diverticulum have similarities. In the present case, the diagnosis of isolated enteric duplication cyst was made since it was found distant from the ileum. It is important to consider the possibility of ectopic pancreatitis when serum pancreatic enzymes are elevated even when the pancreas appears normal.
Enteric duplication is a rare anomaly, which is found along the gastrointestinal tract and generally shares the same blood supply as the nearby intestine . It has been reported to contain ectopic pancreatic tissue in approximately 3% of cases . Isolated enteric duplication cyst is an intestinal duplication cyst occurring in a location independent of the gastrointestinal tract and it has its own blood supply .
A 5-year-old girl with no past medical or surgical history had complained of waxing and waning pain around the umbilicus for a few years. On several occasions, she had visited her general practitioner due to abdominal pain, but no abnormalities had been noted. The pain recurred with greater severity, and abdominal ultrasound performed by her general practitioner revealed a cystic lesion in the right lower abdominal cavity. An abdominal abscess was suspected thus she was referred to a tertiary hospital.
On admission, the vital signs were as follows: blood pressure, 125/81 mmHg; pulse, 166 beats per minute; and temperature; 36.5 °C. On palpation, rebound tenderness was noted on the right iliac fossa. On laboratory investigation, the white blood cell count was 17,400/μL and the C-reactive protein level was 1.54 mg/dl. There was an elevation in the serum pancreatic amylase and lipase level (124 U/L, 114 U/L respectively). Contrast enhanced abdominopelvic computed tomography (CT) (Fig. 1) revealed a cystic lesion measuring 6 × 5 cm with an enhancing thick wall in the ileal mesentery. The cystic lesion was tubular in shape and inflammation was suspected as the density of the adjacent fat was increased. A small enhancing nodule in the cyst wall was also noted. Retrospectively, a distinct blood vessel coursing on the dorsal side into the lesion was identified (Fig. 2). The pancreas appeared within normal limits. The appendix was slightly enlarged and a diagnosis of appendicitis was equivocal.
An abscess in the mesentery was suspected, and the patient was put on nil by mouth and treated with antibiotics. There were significant improvements in the symptoms and the laboratory data on the second week and she was discharged on the fifth week. Follow-up enhanced CT at 3 months showed a significant decrease in size of the cystic mass (Fig. 3). However, the abdominal pain persisted and the possibility of appendicitis with abscess formation was considered, hence laparoscopic appendectomy was performed. After appendectomy, the abdominal pain recurred and a slight elevation of the pancreatic enzymes persisted so a laparoscopy was repeated for possible resection of the mesenteric lesion. During laparoscopy, a cystic mass was found in the root of the iliac mesentery measuring approximately 2 × 1.5 cm in diameter. There was no communication between the mass and the nearby ileum. During the procedure, there was bleeding from the blood vessel coursing dorsal to the mass and hemostasis was required.
Pathologically, the wall of the lesion assimilated the small bowel wall with villi in the mucosa and under the mucosa there was pancreatic tissue consisted of acini, ducts and islets of Langerhans (Fig. 4). The pancreatic duct appeared to open into the cyst. Therefore, a diagnosis of isolated enteric duplication cyst with Heinrich type I ectopic pancreas was made. Changes suggestive of post pancreatitis such as lymphocytes infiltration and acinar loss with islet-cell pseudohyperplasia were also seen in the pancreatic tissue. Postoperatively there were no complications and in the follow-up the serum pancreatic enzymes normalized. The patient reported no recurrence of abdominal pain since the resection of the lesion.
Discussion and Conclusion
Enteric duplication is a rare gastrointestinal anomaly with an incidence of 2 in 9000 among postmortem newborn infants and fetuses . It can occur anywhere along the intestinal tract, although about 44% of duplication cysts are found in the small intestine  and most cases are seen in the ileum. It is defined as a structure consisting of intestinal mucosa surrounded by smooth muscle, and it shares the same smooth muscle and blood supply with the nearby intestine . It has been reported that ectopic gastric mucosa is observed in 20–30% of cases of enteric duplication [6,7,8], while ectopic pancreas is found in 3% of cases .
Some cases of enteric duplication are not anatomically associated with the gastrointestinal tract and are designated as isolated enteric duplication cysts . In contrast to enteric duplication, isolated enteric duplication cysts have their own blood supply. There have been several reported cases of isolated enteric duplication cysts including the tongue, pleural space, liver and pancreas, biliary tree, and retroperitoneum. However, the number of reports is still limited. Another possibility for the diagnosis was mesenteric Meckel’s diverticulum. Meckel’s diverticulum is a remnant of the embryonic vitelline duct which is a tubular structure connecting the yolk sac and the embryonic midgut during the embryonic development. It is obliterated at the 6th – 7th week, but in Meckel’s diverticulum, it fails to obliterate and remains as a diverticulum . Meckel’s diverticulum is the most frequently found anomaly in the gastrointestinal tract, and is found in around 2–3% of the population . Anatomically, Meckel’s diverticulum is found within 100 cm from the ileocecal valve at the antimesenteric side [11, 12] and its wall consists of normal small bowel wall with five layers and it has its own blood supply through the mesodiverticular band. Ectopic gastric mucosa is found in approximately 23–50% of cases [13, 14], while ectopic pancreatic tissue is found in about 5–16% of cases . Ectopic pancreas is most frequently found in the gastrointestinal tract around the pancreas, such as the stomach and duodenum. Meckel’s diverticulum accounts about 5% of all ectopic pancreas cases. Interestingly ectopic pancreas is also found outside the gastrointestinal tract and these include the gallbladder, spleen, lungs and umbilicus . Although one of the cardinal features of Meckel’s diverticulum is its antimesenteric location, there have been a few reported cases of mesenteric Meckel’s diverticulum [17,18,19,20,21]. These reported cases are either ileal diverticulum or a cystic mass with the wall consisted of small intestine in the mesenteric side. However, especially in cystic cases without a communication with the ileum, the diagnosis seems ambiguous.
In the present case, the wall of the cystic lesion consisted of small bowel wall without sharing the smooth muscle with the nearby ileum and it had its own blood supply. Nonetheless its location was at a feasible distance from the ilioceolovalve for Meckel’s diverticulum and pancreatic tissue is observed more frequently in Meckel’s diverticulum, it was distant from the small intestine siting at the root of the mesentery almost in the retroperitoneum. These findings support the diagnosis of an isolated enteric duplication cyst.
We have experienced a case of ectopic pancreatitis in an isolated intestinal duplication. It had a distinguished blood supply and Mesenteric Meckel’s diverticulum was considered for the differential diagnosis. It was located at the root of the mesentery where the lesion was distant from the border of the ileum, thus the diagnosis of ectopic pancreatitis in an isolated intestinal duplication was made. It is important to consider ectopic pancreatitis when serum pancreatic enzymes are elevated even when the pancreas appears normal.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Ladd WE, Gross RE. Surgical treatment of duplication of the alimentary tract. Surg Gynecol Obstet. 1940;70:295–307.
Chiba T, Ohi R. Meckel’s Diverticulum, Duplication of the alimentary tract-pathophysiology and management. Clin Gastroenterol. 1996;11:1813–24.
Steiner Z, Mogilner J. A rare case of completely isolated duplication cyst of the alimentary tract. J Pediatr Surg. 1999;34:1284–6.
Potter EL. Pathology of the fetus and the newborn. Radiology. 1952;58:743–4.
Iyer CP, Mahour GH. Duplications of the alimentary tract in infants and children. J Pediatr Surg. 1995;30:1267–70.
Gross RE, Holcomb GW Jr, Farber S. Duplications of the alimentary tract. Pediatrics. 1952;9:448–68.
Kumar R, Tripathi M, Chandrashekar N, Agarwala S, Kumar A, Dasan JB, et al. Diagnosis of ectopic gastric mucosa using 99Tcm-pertechnetate: Spectrum of scintigraphic findings. Br J Radiol. 2005;78:714–20.
Bhattacharya A, Samujh R, Rao KL, Mittal BR. Long segment jejuno-ileal duplication cyst with ectopic gastric mucosa detected on 99mTc-pertechnetate scintigraphy. Indian J Nucl Med. 2013;28:96–8.
Meckel JF. Ueber die divertikel am darmkanal. Arch Physiol. 1809;9:421–53.
Moore TC. Omphalomesenteric duct malformations. Semin Pediatr Surg. 1996;5:116–23.
Ghahremani GG. Radiology of Meckel’s diverticulum. Crit Rev Diagn Imaging. 1986;26:1–43.
Faris HC, Whitley JE. Angiographic demonstration of Meckel’s diverticulum: case report and review of the literature. Radiology. 1973;108:285–6.
Fich A, Talley NJ, Shorter RG, et al. Does Helicobacter pylori colonize the gastric mucosa of Meckel’s diverticulum? Mayo Clin Proc. 1990;65:187–91.
Swaniker F, Soldes O, Hirschl RB. The utility of technetium 99m pertechnetate scintigraphy in the evaluation of patients with Meckel’s diverticulum. J Pediatr Surg. 1999;34:760–5.
Groebli Y, Bertin D, Morel P. Meckel’s diverticulum in adults: retrospective analysis of 119 cases and historical review. Eur J Surg. 2001;167:518–24.
Nakame K, Hamada R, Suzuhigashi M, Nanashima A, Ieiri S. Rare case of ectopic pancreas presenting with persistent umbilical discharge. Pediatr Int. 2018;60:891–2.
Sarioglu-Buke A, Corduk N, Koltuksuz U, Karabul M, Savran B, Bagci S. An uncommon variant of Meckel’s diverticulum. Can J Surg. 2008;51:E46–7.
Seitun S, Vito LD, Rossi UG, Panetta M, Cabiddu F, Tedeschi U, Viotti A. Perforated Meckel’s diverticulitis on the mesenteric side: MDCT findings. Abdom Imaging. 2012;37:288–91.
Segal SD, Albrecht DS, Belland KM, Elster EA. Rare mesenteric location of Meckel’s diverticulum, a forgotten entity: a case study aboard USS kitty hawk. Am Surg. 2004;70:985–8.
Kurzbart E, Zeitlin M, Feigenbaum D, Zaritzky A, Cohen Z, Mares AJ. Rare spontaneous regression of patent omphalomesenteric duct after birth. Arch Dis Child Fetal Neonatal Ed. 2002;86:F63.
Manukyan MN, Kebudi A, Midi A. Mesenteric Meckel’s diverticulum: a case report. Acta Chir Belg. 2009;109:510–2.
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