scholarly journals Heterozygote Triplets. A Rare Case of Wilkie’s Syndrome

2020 ◽  
Vol 50 (4) ◽  
Author(s):  
Rigoberto Vidal ◽  
Federico Cuenca-Abente ◽  
Diego Ferro
Keyword(s):  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Rare Variant ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Review Of Literature ◽  
Clinical Evolution ◽  
Wilkie’S Syndrome

Wilkie’s Syndrome is a rare cause of small bowel obstruction that rarely occurs in a familiar setting. We report a rare variant, related to heterozygote triplets in a case that underwent laparoscopic duodenojejunostomy to bypass the obstructed segment. During the patient’s clinical evolution, we collected and discussed preoperative and post-operative studies. In addition, we performed a review of literature.

scholarly journals A Rare Case of Ileal Inflammatory Fibroid Polyp with Small Bowel Obstruction

2019 ◽  
Author(s):  
Asfar Ahamed ◽  
Venkatesh Munikrishnan ◽  
Sudeepta Kumar Swain ◽  
Ajay Chanakya Vallabhaneni
Keyword(s):  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Inflammatory Fibroid Polyp ◽  
Fibroid Polyp

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.

scholarly journals A rare case report of small bowel obstruction following colonoscopy

2019 ◽  
Vol 2019 (2) ◽  
Author(s):  
Tetyana Kelly ◽  
Paul Liebenberg ◽  
Adrian Cohen
Keyword(s):  
Case Report ◽  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Rare Case Report

A Rare Case of Clostridium difficile Enteritis and Small Bowel Obstruction

2015 ◽  
Vol 110 ◽  
pp. S409-S410
Author(s):  
Noah Settergren ◽  
Colin Wolslegel ◽  
Henrique Fernandez
Keyword(s):  
Small Bowel ◽  
Clostridium Difficile ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case

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

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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