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http://dx.doi.org/10.1016/j.gastrohep.2013.06.004DOI Listing

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Article Synopsis
  • Intussusception, a bowel obstruction in kids, can sometimes result from serious conditions like Burkitt's lymphoma, as illustrated in a case involving a 14-year-old boy who underwent surgery for ileocolic intussusception.
  • The patient initially experienced abdominal pain, and imaging revealed a mass in the intestine leading to surgical intervention, which confirmed the presence of Burkitt's lymphoma.
  • It's important for doctors to consider underlying diseases like Burkitt's lymphoma in pediatric intussusception cases that don’t respond to standard treatments, as prompt surgical action greatly enhances survival chances.
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Background: Intussusception is a frequent abdominal emergency in the pediatric population when the proximal bowel invaginates into the distal bowel. However, catheter-induced intussusception has not previously been described in pediatric renal transplant recipients, and the risk factors need to be investigated.

Case Description: We report 2 cases of post-transplant intussusception which were caused by abdominal catheters.

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Intussusception is a rare condition in adults that can lead to intestinal obstruction due to malignant or benign lesions in the wall of the colon. Among the benign causes, lipomas are adipose tissue tumors that are most frequently located in the ascending colon. Invagination is characterized by nonspecific symptoms and normal laboratory test results.

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Background: We aimed to present cecum pathologies which are the cause of acute abdomen.

Methods: Between January 2015 and June 2019, patients that were operated with the diagnosis of acute abdomen and patients with the primary cecum pathologies were evaluated retrospectively.

Results: There were eight patients, five males and three females.

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Intestinal intussusception occurs when a proximal segment of the intestine telescopes into the lumen of an adjacent distal segment, causing intestinal obstruction. It is a common cause of acute abdomen in the first two years of life, but rare in older children. A 16-year-old male with a diagnosis of cystic fibrosis presented with symptoms compatible with distal intestinal occlusion syndrome.

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