benign polyp
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2021 ◽  
Vol 108 (Supplement_7) ◽  
Author(s):  
Armin Fardanesh ◽  
Jamie Powell ◽  
Maitham Al-Whouhayb

Abstract Introduction Roux-en-Y Gastric bypass (REYGB) amounts for a third of surgical bariatric interventions. Small bowel obstruction (SBO) is a long-term complication in REYGB and can be caused by intussusception of bowel, in approximately 0.5% of procedures.  Intussusception in REYBG is mostly attributed to dysmotility. This report demonstrates a rare case of intussusception in REYGB secondary to a benign polyp.  Case description A 45 year old female, three years post REYGB, presented to A&E with acute, extreme upper abdominal pain, with three days absolute constipation. She was tender on examination with normal blood tests. CT scan demonstrated small bowel intussusception. Initial concerns were of intussusception of the jejuno-jejunostomy anastomosis causing SBO.  She had an exploratory laparotomy, which confirmed intussusception, however this was 20cm distal to the jejuno-jejunostomy. Bowel was gently reduced, and deemed viable. On thorough run-through, a small segment at the transition point, was considered abnormal on palpation. This region was resected and a 1x1cm intraluminal polyp was identified as the causative lead point. The patient did well postoperatively.  Discussion Small bowel intussusception in adults is typically attributed to pathological lead point, such as benign or malignant lesions. Intussusception in REYBG is a rare but well-documented cause of intestinal obstruction, usually attributed to dysmotility, secondary to ectopic pacemaker cells particularly around anastomoses. In this case, the intussusception was caused by an unusual pathology separate from the jejuno-jejunal anastomosis. We recommend thorough examination of all adjacent bowel to exclude lesions, in this case a polyp, which could result in recurrence. 


2021 ◽  
Vol 116 (1) ◽  
pp. S785-S785
Author(s):  
Joseph Asemota ◽  
Temitayo Gboluaje ◽  
Adeyinka Laiyemo ◽  
Angesom Kibreab ◽  
Victor Scott ◽  
...  
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Author(s):  
Joceline V. Vu ◽  
Kyle H. Sheetz ◽  
Ana C. De Roo ◽  
Tadd Hiatt ◽  
Samantha Hendren

Author(s):  
Shigetoshi Naito ◽  
Masayasu Naito ◽  
Nobuharu Yamamoto ◽  
Tohru Kume ◽  
Seiichirou Hosino ◽  
...  

2019 ◽  
Vol 12 (9) ◽  
pp. e230612
Author(s):  
Adrian K McGrath ◽  
Fatimah Suliman ◽  
Noel Thin ◽  
Ashish Rohatgi

Meckel’s diverticulum is the most common congenital abnormality affecting the gastrointestinal tract, affecting 4% of the general population. It is classically located on the antimesenteric border of the ileum within 100 cm of the ileocaecal valve. Complications may include haemorrhage, bowel obstruction, diverticulitis, perforation and malignancy. This report explores the case of intussusception in an adult, in association with a mesenteric Meckel’s diverticulum and adjacent benign polyp. A 40-year-old man presented with acute abdominal pain, affecting the central abdomen and both flanks. CT imaging revealed small bowel intussusception, with either a Meckel’s diverticulum or polyp acting as a lead point. Intraoperatively, the intussusception had already resolved; however, an inflamed outpouching was identified on the mesenteric border of the ileum, with a firm mass palpable within the bowel lumen. A 70 mm small bowel resection and primary anastomosis were performed. Histopathological analysis confirmed an inflamed Meckel’s diverticulum as well as an adjacent diverticulum comprising a benign polyp.


2019 ◽  
Vol 156 (6) ◽  
pp. S-1384-S-1385
Author(s):  
Dasuni Niyagama Gamage ◽  
Neil Mitra ◽  
Jaspreet Sandhu ◽  
Tianyi Lu ◽  
Vesna Cekic ◽  
...  
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2016 ◽  
Vol 36 (3) ◽  
pp. 176-178
Author(s):  
Şafak Meriç Özgenel ◽  
Tuncer Temel ◽  
Evrim Yılmaz ◽  
Salih Tokmak ◽  
Ayşegül Özakyol

2016 ◽  
Vol 39 (6) ◽  
pp. 478-480 ◽  
Author(s):  
Omer Ozturk ◽  
Seyfettin Koklu ◽  
Cenk Sokmensuer ◽  
Halt Uner
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2014 ◽  
Vol 04 (02) ◽  
pp. 147-148
Author(s):  
Sandeep B. Rai ◽  
Raghu Shankar

Abstract:Urethral polyp is a rare finding in young children. These are congenital fibroepithelial benign polyp in the prostatic urethra. They present with acute or intermittent urinary obstruction, hematuria or voiding dysfunction. Their diagnosis requires a high index of suspicion because of variability in presentation. Diagnosis can be made by ultrasonography or micturating cystourethrogram, however cystourethroscopy is confirmatory. Transurethral resection is possible in almost all the cases and recurrence is almost unknown. We report a case of this rare lesion in a male infant with a severe phimosis.


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