Concurrent intestinal malrotation and Meckel's diverticulum presenting as acute intestinal obstruction in an adult

Authors

  • Aishwarya Emerald Manohar Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India
  • M. S. Kalyan Kumar Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India
  • V. Vijayalakshmi Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India
  • R. Kannan Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

DOI:

https://doi.org/10.18203/2349-2902.isj20212288

Keywords:

Intestinal malrotation, Meckel’s diverticulum, Adult, Ladd's band

Abstract

Intestinal malrotation is the partial or complete failure of rotation of midgut around the superior mesenteric artery, while Meckel’s diverticulum is the remnant of vitellointestinal duct and concurrence of these congenital abnormalities in an adult is considered a rarity. Till date only 3 cases of concurrent intestinal malrotation and Meckel's diverticulum have been reported. We report a 18 years male who presented with a 3 day history of abdominal pain, bilious vomiting, obstipation and chronic abdominal pain on and off since 3 years of age. During the last episode which occurred 1 year back, he was diagnosed with intestinal malrotation with subacute intestinal obstruction and was treated conservatively. Examination revealed the presence of signs of peritonitis. After resuscitation, CECT abdomen was taken which showed dilated small bowel loops in the subhepatic region associated with malrotation. Emergency laparotomy revealed a Ladd's band below which the gangrenous small bowel loops 150 cm from the duodenojejunal (flexure until 5 cm proximal to the ileocecal junction) were found herniating into the subhepatic region with a Meckel’s diverticulum and a right sided DJ flexure. We proceeded with the band release and resection of gangrenous bowel followed by proximal jejunostomy with distal ileostomy. HPE was consistent with Meckel’s diverticulitis without any ectopic gastric or pancreatic mucosa. Ostomy reversal was done after 8 weeks. Patient had an uneventful postoperative recovery during both the admissions and he is on regular follow-up now.

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Author Biographies

Aishwarya Emerald Manohar, Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

General Surgery

M. S. Kalyan Kumar, Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

General Surgery

V. Vijayalakshmi, Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

General Surgery

R. Kannan, Institute of General Surgery, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

General Surgery

References

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Sondheimer J. Current essentials: pediatrics. 1st ed. New York, NY: McGraw Hill; 2008: 50-51.

Harvey JS, Giles GR. Associated midgut malrotation and Meckel's diverticulum presenting in adult life. Br J Surg. 1974;61(2):157-8.

Weitzman JJ, Brennan LP. Bronchogastric fistula, pulmonary sequestration, malrotation of the intestine, and Meckel's diverticulum-a new association. J Pediatr Surg 1998;33:1655-7.

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Published

2021-05-28

How to Cite

Manohar, A. E., Kumar, M. S. K., Vijayalakshmi, V., & Kannan, R. (2021). Concurrent intestinal malrotation and Meckel’s diverticulum presenting as acute intestinal obstruction in an adult. International Surgery Journal, 8(6), 1904–1906. https://doi.org/10.18203/2349-2902.isj20212288

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Section

Case Reports