Intussusception of Invaginated Meckel's Diverticulum
نویسندگان
چکیده
منابع مشابه
Meckels diverticulum and intestinal ischaemia
We report an exceptional case of intestinal ischaemia requiring resection, secondary to torsion around a long Meckel's diverticulum. Meckel's diverticulum is an uncommon congenital abnormality of the small bowel. Meckel's diverticulum giving rise to intestinal ischaemia that requires resection is very rare but potentially fatal complication. A 62 year old woman presented as an emergency with su...
متن کاملManagement of asymptomatic or incidental Meckels diverticulum.
This study was conducted to compare the clinicopathologic characteristics of incidentally found and symptomatic cases of Meckels diverticulum with the aim of arriving at a recommendation regarding the management of incidental cases. A retrospective chart review was performed over a period of 24 years. Incidental group had 52 patients and symptomatic group had 128 patients(71%). Obstruction (42....
متن کاملInvaginated Meckel's diverticulum: a rare cause of small intestine intussusception in adults.
Intussusception is commonly seen in infants. It is occasionally found in adults usually due to carcinomas, colonic diverticuli, polyps and rarely Meckel's diverticulum. An adult male presented with upper abdominal pain, nausea, anorexia and loose stools. The initial investigative workup was unremarkable and patient responded to treatment given for acute gastroenteritis. After 3 days, the pain r...
متن کاملMeckels Diverticulum Causing Volvulus of Ileum
The most common complications of Meckel’s diverticulum are Intestinal obstruction, gastrointestinal haemorrhage, adherence, intussusception, acute diverticulitis and rarely malignancy. Reported mechanism of intestinal obstruction in Meckel’s diverticulum include invagination, adherence and volvulus. Obstruction of ileum caused by volvulus of Meckel’s diverticulum is not a very frequent conditio...
متن کاملMeckel’s diverticulum-induced ileocolonic intussusception
A previously healthy 8-year-old male complained of severe, intermittent and stabbing abdominal pain that had waxed and waned over the past 3 days. At the time of presentation, the pain was right-sided, peri-umbilical and non-radiating. He denied nausea, vomiting, hematochezia, melena or urinary tract symptoms; he had however experienced several recent episodes of brown diarrhea. On physical exa...
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1984
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107688407700808