An unusual complication of Meckel’s diverticulum: Littre’s hernia
Tariq Bouhout, Badr Serji, Ebo Usman Egyir, Benyounes El Amri, Imad Bouhout, Mehdi Soufi, Mohammed Bouziane, Tijani El Harroudi
Received: 15 Sep 2016 - Accepted: 17 Oct 2016 - Published: 21 Dec 2018
Domain: Clinical medicine
Keywords: Littre´s hernia, Meckel´s diverticulum, intestinal obstruction
©Tariq Bouhout et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Tariq Bouhout et al. An unusual complication of Meckel’s diverticulum: Littre’s hernia. Pan African Medical Journal. 2018;31:243. [doi: 10.11604/pamj.2018.31.243.10740]
Available online at: https://www.panafrican-med-journal.com/content/article/31/243/full
An unusual complication of Meckel’s diverticulum: Littre’s hernia
Tariq Bouhout1,&, Badr Serji1, Ebo Usman Egyir1, Benyounes El Amri2, Imad Bouhout2, Mehdi Soufi2, Mohammed Bouziane2, Tijani El Harroudi1
1Chirurgie B, CHU Mohammed VI, Oujda, Maroc, 2Chirurgie A, CHU Mohammed VI, Oujda, Maroc
Tariq Bouhout, Chirurgie B, CHU Mohammed VI, Oujda, Maroc
Meckel diverticulum is the most common congenital anomaly of the gastrointestinal tract. Any hernia sacs containing Meckel’s diverticulum is called Littre’s hernia.It was described for the first time in 1700 by Alexis Littre. The diagnosis is unlikely to be made preoperatively and Surgery is the treatment of choice. We report a rare case of Littre’s hernia who presented with clinical signs of intestinal obstruction.
Meckel’s diverticulum is found at the antimesenteric border of the ileum, usually located from 30 to 90 cm from the ileocecal valve. Any hernia containing the Meckel’s diverticulum is termed a Littre’s hernia.Littre’s hernia is a rare anatomoclinical form; it was described for the first time in 1700 by Alexis Littre . The diagnosis is unlikely to be made preoperatively.
A 39-year-old previously healthy woman was admitted at the emergency service with clinical signs of intestinal obstruction. Physical examination revealed a mass at right inguinal area which was not reducible or pulsatile. Abdominal radiographs showed small bowel obstruction. A diagnosis of strangulated inguinal hernia was made. Operation was done under general anesthesia, a median incision was performed, on exploration a strangulated Meckel’s diverticulum was found in the sac of obstructed inguinal hernia (Figure 1). The diverticulum measured 2cm and was located on the antimesenteric surface, 90 cm from the ileocecal valve. Due to the broad base and necrosis of the Meckel’s diverticulum (Figure 2), a small bowel segment was resected (Figure 3) and continuity of ileum restored by an end to end anastomosis. The patient made a rapid and uneventful post operative recovery.
Meckel’s diverticulum is the most prevalent congenital abnormality of the gastrointestinal tract. The incidence of Meckel’s diverticulum is 2% and normally it is not symptomatic . Meckel diverticulum occur on the antimesenteric border of the ileum, generally at a distance of about 30 to 90 cm from the ileocecal valve . In 1700,Alexis Littre, a French surgeon was the first to report three cases of incarcerated femoral hernia containing a small bowel diverticulum , since then, hernia sacs containing Meckel’s diverticulum have been called Littre’s hernia . It is a rare anatomoclinical form representing 10% of all complications of Meckel’s diverticulum . Approximately 50% of Littre hernias occur in the inguinal regio n, 20% in the femoral region, 20% in the umbilical region and 10% in other locations . Because of its low incidence, Littre’s hernia is generally unsuspected and the diagnosis is unlikely to be made preoperatively.
However Sinha reported the first case of an incarcerated Littre hernia diagnosed on computerised tomography . The Meckel diverticulum was seen in the hernia sac as a tubular blind-ending structure arising and communicating with the distal ileum. Surgery is the treatment of choice; the diverticulum is locally excised and small intestine sutured transversely, however if the base is wide and if there is an inflammation at the base of the diverticulum, resection of the involved loop of ileum with anastomosis is the preferred procedure, as was done for our case. So the question arises, it is necessary to resect an incidentally discovered Meckel’s diverticulum? Resection had been the subject of controversy. Some authors advocate the resection of the diverticulum because post-operative morbidity and mortality is very low, whereas others see that resection is not justified because complications are rare. We think that criteria for the resection of Meckel’s diverticulum found incidentally should be suggested.
An unusual complication of Meckel’s diverticulum, a strangulated Littre’s inguinal hernia is presented. The symptoms and physical findings in this type of hernia are deceptively few; the preoperative diagnosis is usually incarcerated hernia. Surgery is the main stay of treatment.
The authors declare no competing interests.
All authors contributed equally in the literature search, interpretation of the articles and review of the manuscript. All the authors have read and approved the final version of the manuscript.
Figure 1: strangulated Meckel’s diverticulum in the sac of obstructed inguinal hernia
Figure 2: Meckel’s diverticulum located on the antimesenteric surface, 90 cm from the ileocecal valve
Figure 3: operative specimen
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