Skip to main content
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association logoLink to Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association
letter
. 2011 May-Jun;17(3):222–223. doi: 10.4103/1319-3767.80392

Knotting of Ileum by Meckel’s Diverticulum Leading to Acute Small Bowel Obstruction: An Exceptional Case

Vipul D Yagnik 1, Bhargav D Yagnik 1
PMCID: PMC3122099  PMID: 21546731

Sir,

A 12-year-old male came to the emergency room with complaints of right iliac fossa pain and abdominal distention since the last 48 h. This was associated with nausea, vomiting, and absolute constipation. Abdominal examination finding revealed a generalized distention with localized guarding and rigidity in the right lower quadrant. Bowel sounds were hyperperistaltic. Examination revealed BP of 100/70 mmHg, pulse rate of 100/min, and temperature of 38°C. Laboratory data showed white cell count of 20,000/mm 3with left shift. A plain radiograph of the abdomen erect revealed intestinal obstruction. On opening the abdomen, knotting of Meckel’s around the small bowel was seen. Knot was untied and the diverticulum released [Figure 1]. Resection of the gangrenous Meckel’s diverticulum and short segment of ileum and anastomosis was performed. Postoperative course was unremarkable.

Figure 1.

Figure 1

Released Meckel’s with constriction mark at the base withdilated proximal bowel

Meckel’s diverticulum is the most frequent congenital anomaly of the gastrointestinal tract, is located on the antimesenteric border of ileum 2 ft proximal to the ileocecal junction. It is named after Johann Meckel, who described it in detail in 1809.[1] Meckel’s diverticulum is a true diverticulum, possesses all three coats of the intestinal wall, and has its own blood supply.[2] The size is variable with average length being 5 cm and the arterial supply is derived from the persistent vitelline artery arising from the superior mesenteric artery or less frequently ileocolic artery.[3] The majority of cases are asymptomatic. If symptomatic, it can present as bleeding per rectum, intestinal obstruction, or diverticulitis.

Knotting of ileum by Meckel’s diverticulum is a rare presentation of Meckel’s leading to acute small bowel obstruction.[4] This case is exceptionally unusual as knotting was not associated with internal hernia and only tip of the Meckel’s was gangrenous. After initial resuscitation, management of such cases includes either laparoscopic or open surgery.

REFERENCES

  • 1.Opitz JM, Schultka R, Gobbel L. Meckel on developmental pathology. Am J Med Genet A. 2006;140:115–28. doi: 10.1002/ajmg.a.31043. [DOI] [PubMed] [Google Scholar]
  • 2.Yammaguchi M, Tacheuchi S, Awazu S. Meckel’s diverticulum, investigation of 600 patients in Japanese literature. Am J Surg. 1978;136:247–9. doi: 10.1016/0002-9610(78)90238-6. [DOI] [PubMed] [Google Scholar]
  • 3.Rossi P, Gourtsoyiannis N, Bezzi M, Raptopoulos V, Massa R, Capanna G, et al. Meckel’s diverticulum: Imaging diagnosis. AJR Am J Roentgenol. 1996;166:567–73. doi: 10.2214/ajr.166.3.8623629. [DOI] [PubMed] [Google Scholar]
  • 4.Thakor AS, Liau SS, O’riordan DC. Acute small bowel obstruction as a result of Meckel’s diverticulum encircling the terminal ileum: A case report. J Med Case Reports. 2007;1:8. doi: 10.1186/1752-1947-1-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association are provided here courtesy of Wolters Kluwer -- Medknow Publications

RESOURCES