Intussusception caused by an inverted Meckel diverticulum: a rare cause of small bowel obstruction in adults

Intussusception caused by an inverted Meckel diverticulum: a rare cause of small bowel obstruction in adults

 

Mahdi Bouassida^1,&, Bilel Feidi¹, Mechaal Ben Ali², Mohamed Fadhel Chtourou¹, Marouene Krifa², Selim Sassi¹, Fathi Chebbi¹, Mohamed Mongi Mighri¹, Hassen Touinsi¹, Sadok Sassi¹

 

¹Department of surgery, Mohamed Thahar Maamouri Hospital, Nabeul, Tunisia, ²Department of reanimation, Mohamed Thahar Maamouri Hospital, Nabeul, Tunisia

 

 

^&Corresponding author
Mahdi Bouassida, Department of surgery, Mohamed Thahar Maamouri Hospital, 8000 Mrazga, Nabeul, Tunisia

 

 

Meckel’s diverticulum is the most common congenital abnormality of the gastrointestinal tract, occurring in 1% to 2% of the population. It is usually asymptomatic and becomes evident when complicated. Intestinal obstruction due to Meckel´s diverticulum is the most common presentation in adult and is the second most common in children. Occasionally, inversion of Meckel’s diverticulum into the lumen of the bowel can cause intussusception, ischemia and infarction. The incidence of intussesception attributed to an inversion of Meckel’s diverticulum accounts for 4% of all cases presenting with intestinal obstruction due to intussusception.

 

It occurs when the Meckel’s diverticulum sags into the bowel lumen and then serves as a lead point to allow telescoping of the small intestine, first into the distal ileum and then in to the large intestine, causing ileo-ileal and ileocolic type of intussusceptions.

 

 

A 22-year-old male presented to the emergency room complaining of abdominal pain and vomiting for one day. He had no significant past medical history or previous abdominal surgery. There was no family history of any hereditary illnesses. On admission he had normal vital signs and a temperature of 38°C. Physical examination showed a slightly distended abdomen with hyperactive bowel sounds. The patient had abdominal tenderness and muscle guarding. No masses or hernias were identified. Laboratory tests revealed increased white blood cells (WBC) of 13 200 µ/L. Plain abdominal X-ray demonstrated air fluid levels of the small bowel, there was no pneumoperitomeum. We diagnosed an acute small bowel obstruction. Because of severe abdominal pain, the patient underwent emergency surgery with a lower midline abdominal incision. The intra operative findings were distention of the small bowel and intussusception of ileus due to an inverted Meckel’s diverticulum located 70 cm from the ileocecal valve. 30 cm ischemic loop was identified (Figure 1). A segmental small bowel resection and hand-sewn anastomosis was performed.

 

Histopathology revealed Meckel’s diverticulum measuring 5 cm x 3.5 cm x 1 cm without ectopic mucosa or malignancy. The postoperative period was uneventful and after 7 days the patient was discharged. At the 6 months follow-up, the patient had no evidence of complications.

 

 

Intestinal obstruction due to Meckel´s diverticulum is the most common presentation in adult and is the second most common in children [1]. There are various mechanisms by which it can cause intestinal obstruction like (a) Volvulus of small intestine around a fibrous band extending from Meckel´s diverticulum to umbilicus. (b) Intussusception – in which Meckel diverticulum sags into the bowel lumen and then serves as a lead point to allow telescoping of the small intestine into first the distal ileum and then in to the large intestine causing ileo-ileal and ileocolic type of intussusception. (c) Littre´s hernia – Incarceration of the diverticulum in hernia, (inguinal and femoral) causing intestinal obstruction. (d) Entrapment of small bowel beneath the blood supply of the diverticulum, also known as a mesodiverticular band (e) Stricture secondary to chronic diverticulitis [2] (f) Meckel´s diverticulum lithiasis (g) Band extending between the diverticulum and the base of the mesentery, forming a loop in which a part of ileum may get stuck causing obstruction [3]. Inversion of Meckel diverticulum is not yet clearly understood. One theory is that abnormal peristaltic movement due to ulceration or ectopic tissue at the base of Meckel diverticulum may cause it to invert [4]. The presenting symptoms in adult patients with intussusceptions are nonspecific and often long-standing. The most important characteristic of pain is its periodic, intermittent nature, which makes the diagnosis elusive and accounts for the delay in establishing the diagnosis [5]. CT is the most sensitive imaging modality for diagnosis of bowel obstruction with reported accuracy of 58%-100% [6]. In the early stage, the characteristic point is the target lesion, described as enveloped, eccentrically located areas of low density, which represents the intussuscepted bowel viewed in cross section [7]. Other findings, such as vascular compromise, layering or stratification effect to bowel wall thickening and amorphous mass are recognized later in the natural history of unrelieved intussusceptions [8].

 

Intra operatively, the intussuscepted bowel should be deployed and examined for ischemia. There is no doubt that in case of transmural ischemia, the bowel needs to be resected along with the diverticulum [9]. Intussusception due to Meckel’s diverticulum is an absolute indication for Meckel’s diverticulum resection [8]. Recently, the prevalence of laparoscopic surgery has been increasing. However, the procedure should be chosen carefully because of an increased risk of perforation [8]. In our case, the abdomen was hard with tenderness and muscle guarding, and the leukocyte count was increased. These findings suggested an intussusceptions caused by benign lesion, but we did not choose a laparoscopic procedure because we considered that a lengthy segment of intestine was necrotic.

 

 

Adult intussusception caused by inverted Meckel’s diverticulum may be observed in any age. It is a rare but important clinical entity. The presenting symptoms of intussusception are nonspecific. Diverticulectomy or bowel resection is the standard treatment.

 

 

The authors declare no competing interests.

 

 

MB, BF, MBA and MFC performed the surgical procedure and reported the case. MK, SS and FC participated in the diagnostic and therapeutic decisions. MMM, HT and SS made major contributions in writing the manuscript. All authors read and approved the final manuscript.

 

 

Figure 1: The surgical specimen after reduction comprised a 30 cm segment of resected ileus with an elongated polypoid lesion (arrow) within the ileal lumen, and a lengthy segment of intestine was necrotic

 

 

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