1338 A Rare Case of Duodenal Windsock Diverticulum; Simultaneous Biliary, and Small Bowel Obstruction

2019 ◽  
Vol 114 (1) ◽  
pp. S741-S741
Author(s):  
Muhammad H. Bashir ◽  
Lilly Gonzalez ◽  
Yaniuska Lescaille ◽  
Bridget Gallagher ◽  
Derrick Cheung
Keyword(s):  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case

scholarly journals Closed loop bowel obstruction secondary to left paraduodenal hernia (of Landzert)

2019 ◽  
Vol 12 (12) ◽  
pp. e232134
Author(s):  
Yeo Min Cho ◽  
Gamze Aksakal ◽  
Mohamed Ahmed Tawfik Ashour ◽  
Suzanne Moore
Keyword(s):  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Closed Loop ◽  
Flank Pain ◽  
Paraduodenal Hernia ◽  
Good Recovery ◽  
Left Colic Artery ◽  
Unusual Phenomenon

A 34-year-old man presented with acute severe left-sided abdominal and flank pain with associated postprandial nausea and vomiting. CT imaging revealed findings suspicious for a closed loop small bowel obstruction. Intraoperative findings were that of a left paraduodenal hernia (of Landzert) secondary to a mesenteric defect immediately posterior to the ascending branch of the left colic artery. The defect was closed via minilaparotomy. Unfortunately, his postoperative course was complicated by small bowel obstruction which required further laparotomy and adhesiolysis. The patient eventually made a good recovery. Here, we present a rare case of intestinal obstruction and discuss the aetiologies and management of this unusual phenomenon.

Transmesocolic internal herniation: a rare case of small bowel obstruction, “the Marrakesh hernia”

Hernia ◽  
2009 ◽  
Vol 14 (4) ◽  
pp. 427-429 ◽  
Author(s):  
Y. Narjis ◽  
R. Jgounni ◽  
M. N. El Mansouri ◽  
K. Rabbani ◽  
R. Hiroual ◽  
...  
Keyword(s):  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Internal Herniation

scholarly journals CASE REPORT : RARE CASE OF SMALL BOWEL OBSTRUCTION DUE TO MECKELS DIVERTICULUM

2021 ◽  
Vol 9 (06) ◽  
pp. 641-644
Author(s):  
Simranjit Kaur Dhadiala ◽  
◽  
Abhijit A. Whatkar ◽  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Rare Congenital Anomaly ◽  
Meckels Diverticulum ◽  
Male To Female

Meckels diverticulum is a rare congenital anomaly of gastrointestinal tract, seen in 2% of population. It was first described by Guilhemus Fabricus Hildonus in 1598. Meckels diverticulum is an anomaly derived from incomplete obliteration of omphalo-mesenteric duct. It is rarely seen in adults, with prevalence of male to female of 2:1. Complications associated with Meckels diverticulum are hemorrhage, inflammation and intestinal obstruction. We present to you a case of 17 year old male with unusual mechanism of small bowel obstruction due to Meckels diverticulum.

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