Double Trouble: a Rare Case of Small Bowel Intussusception Secondary to Neuroendocrine Tumour Within a Meckel’s Diverticulum

Author(s):  
Tetyana Kelly ◽  
Samriti Sood
2020 ◽  
Vol 90 (10) ◽  
pp. 2108-2110
Author(s):  
Joshua A. De Bono ◽  
Jonathan Sivakumar ◽  
Sam Norden ◽  
Mark Cullinan

2016 ◽  
pp. bcr2016214830 ◽  
Author(s):  
Syed Hussain Abbas ◽  
Khalid Akbari ◽  
John Mason ◽  
Michael Booth

2021 ◽  
Vol 8 (4) ◽  
pp. 1289
Author(s):  
Nusrat Jabeen ◽  
Hussain Adnan Abdulla ◽  
Asma Alqaseer ◽  
Mohamed Ayed Abushwemeh ◽  
Amal Alrayes

Meckel’s diverticulum is the most common congenital abnormality of the gastrointestinal tract. Complications involving Meckel’s diverticulum include bleeding, bowel obstruction and inflammation. We present a rare case of small bowel obstruction caused by Meckel’s diverticulum. A 50-year-old male presented to the emergency department with abdominal pain and vomiting. Computed tomography (CT) abdomen showed dilated small bowel loops with transition zone at the mid ileum, consistent with small bowel obstruction. The patient was taken to the operating theatre for exploratory laparotomy and was found to have a Meckel’s diverticulum causing mechanical small bowel obstruction, which was resected with primary anastomosis. The patient recovered with no postoperative complications and was discharged home. Meckel’s diverticulum is difficult to diagnose preoperatively since most patients are asymptomatic and requires a high index of suspicion. In patients presenting with an acute abdomen, it may be overlooked because of nonspecific symptoms. In the case of small bowel obstruction, Meckel’s diverticulum should be kept in mind as part of the differential diagnosis.


2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Daniel John Marascia

Intussusception secondary to inverted Meckel’s diverticulum resulting in intestinal obstruction is rare. The following is a case report that discusses a 29-year-old female who posed diagnostic uncertainty for the treating surgical team and ultimately underwent emergency surgery for the management of intestinal obstruction. Small bowel intussusception was diagnosed preoperatively on abdominal computer tomography (CT). At operation, it was found to be secondary to inverted Meckel’s diverticulum with histopathology confirming the diagnosis.


2017 ◽  
Vol 20 (1) ◽  
pp. 63-65 ◽  
Author(s):  
Debra S Heller ◽  
Ada Baisre ◽  
Christian Curcio ◽  
Nawar Matti ◽  
Dianne Sinquee

Meckel’s diverticulum is a congenital anomaly present in about 3% of the population and usually asymptomatic. Rarely, a mesodiverticular band extends from the tip of a Meckel’s diverticulum to the mesentery, thought to be due to lack of involution of the left vitelline artery. The presence of this band creates a closed loop through which loops of bowel can become entrapped. Rare case reports have described incarceration of bowel and sudden death in children. We present such a case and discuss this entity.


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