Literature DB >> 21546731

Knotting of ileum by Meckel's diverticulum leading to acute small bowel obstruction: an exceptional case.

Vipul D Yagnik, Bhargav D Yagnik.   

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Year:  2011        PMID: 21546731      PMCID: PMC3122099          DOI: 10.4103/1319-3767.80392

Source DB:  PubMed          Journal:  Saudi J Gastroenterol        ISSN: 1319-3767            Impact factor:   2.485


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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

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

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.
  4 in total

Review 1.  Meckel's diverticulum: imaging diagnosis.

Authors:  P Rossi; N Gourtsoyiannis; M Bezzi; V Raptopoulos; R Massa; G Capanna; V Pedicini; M Coe
Journal:  AJR Am J Roentgenol       Date:  1996-03       Impact factor: 3.959

2.  Meckel's diverticulum. Investigation of 600 patients in Japanese literature.

Authors:  M Ymaguchi; S Takeuchi; S Awazu
Journal:  Am J Surg       Date:  1978-08       Impact factor: 2.565

3.  Meckel on developmental pathology.

Authors:  John M Opitz; Rüdiger Schultka; Luminita Göbbel
Journal:  Am J Med Genet A       Date:  2006-01-15       Impact factor: 2.802

4.  Acute small bowel obstruction as a result of a Meckel's diverticulum encircling the terminal ileum: A case report.

Authors:  Avnesh S Thakor; Siong S Liau; Dermot C O'riordan
Journal:  J Med Case Rep       Date:  2007-03-23
  4 in total
  2 in total

1.  Neonatal intestinal obstruction secondary to a floppy Meckel's diverticulum successfully treated by minimal access surgery.

Authors:  Dayang Anita Abdul Aziz; Syariz I Sehat; Marjmin Osman; Faizah Mohd Zaki
Journal:  BMJ Case Rep       Date:  2012-12-14

2.  Appendicular knot - an exceptionally rare "two in one case" of acute abdomen.

Authors:  Jotinder Khanna
Journal:  Saudi J Gastroenterol       Date:  2011 Sep-Oct       Impact factor: 2.485

  2 in total

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