Patent vitellointestinal duct with inverted ileal loop prolapse: A rare presentation

2015 ◽  
Vol 4 (2) ◽  
pp. 95 ◽  
Author(s):  
YogenderSingh Kadian
2017 ◽  
Vol 13 (3) ◽  
Author(s):  
Karan Raheja ◽  
Rajeev Aggarwal ◽  
Ashish Prakash ◽  
Arun Kumar ◽  
Himanshu Sharma ◽  
...  

2017 ◽  
Vol 20 ◽  
pp. 14-16
Author(s):  
Fariha Akil Fazal ◽  
James Muturi Ndungu ◽  
Humdun Said ◽  
Josephat Njiru ◽  
Fred Kambuni

2020 ◽  
Vol 7 (5) ◽  
pp. 1662
Author(s):  
M. S. Kalyan Kumar ◽  
Shyamsundar R. ◽  
Sabari Girieasan M. ◽  
R. Kannan ◽  
S. Nedunchezhiyan

Primary internal hernias are very rare in adults. They are an unusual cause of small intestinal obstruction and lead to high morbidity and mortality if left untreated. Clinical presentation of internal hernia is highly nonspecific. Imaging has limited role in diagnosing the cause of acute intestinal obstruction. Internal hernias are usually detected at laparotomy. We report a case of a 61-year-old male who presented with acute intestinal obstruction which was attributed later to a very rare type of internal hernia on exploratory laparotomy. A loop of ileum was found to enter the retroperitoneum through a hernia gate which was located lateral to the caecum and ileo ileal intussusception was noted proximal to the herniated loop. The segment of intestine was resected and anastamosed then hernial defect was closed. Paracaecal hernias are the rare type of hernias in internal hernia. In our case, intussusception was noted proximal to the herniated ileal loop which is a very rare presentation. Intussusception was reported previously with paraduodenal type. One should always keep in mind while conducting emergency laparotomy, internal hernias can be a cause for intestinal obstruction.


2015 ◽  
Vol 15 ◽  
pp. 30-31 ◽  
Author(s):  
Harnam Singh Rekhi ◽  
Sushil Mittal ◽  
Gurtej Singh ◽  
Balwinder Kaur Rekhi ◽  
Pankaj Dugg

2019 ◽  
Vol 7 (5) ◽  
pp. 797-800
Author(s):  
Handayani Handayani ◽  
Yamoguna Zega ◽  
Tati Ziliwu ◽  
Faldi Yaputra ◽  
Nora Minori

BACKGROUND: Prolapse of the small intestine through the umbilicus is indeed a rare presentation and is the most significant complication of the patent omphalomesenteric duct which requires pediatric surgical emergency due to its significant increase of mortality. To date, it is less than twenty cases of this presentation have been reported in medical literature. We are reporting a case of the same in an infant presenting with it on 1st week after he was delivered, but was followed by ileal rupture as well. CASE PRESENTATION: We present a case of a patent omphalomesenteric duct with ileal prolapse and ileal rupture as its complication. It is a case of a 1-year-old infant with a history of unusual bleed-on-touch mass emerging from the anterior abdominal wall with absent umbilicus. Once his condition is stabilised, he underwent a reduction of the prolapsed bowel along with complete excision of the omphalomesenteric duct and restoration of the ileal continuity. Post-operatively he regained normal bowel function and resumed breastfeeding 5 days after surgery. CONCLUSION: This case is an important addition to the literature about patent omphalomesenteric duct with complications of inverted proximal ileal loop prolapse and ileal rupture.


2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Elroy Patrick Weledji ◽  
Martin Mokake ◽  
Marcelin Ngowe Ngowe

We present a case of an unsual type of obstructed indirect inguinal hernia with impending strangulation. The operative findings revealed a sliding Maydl’s hernia with an ischemic inner ileal loop and an adherent inflamed appendix. This case highlights the importance of intraoperative examination of the intra-abdominal bowel loops proximal to the hernia sac of an incarcerated, obstructed, or strangulated hernia.


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