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Intussusceptions arising from two different sites in a child with cystic fibrosis
Gaudenz M Hafen1, Andrew C Taylor, Mark R Oliver
1Department of Respiratory Medicine, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia. gaudi.hafen@rch.org.au
Abstract:
Abdominal pain is common in individuals with cystic fibrosis (CF). We report on a 17-year old boy with CF and two recognized intussusceptions: the first colonic intussusception was presumed due to distal intestinal obstruction syndrome, and the second enteric one due to polypoid lesions containing heterotopic gastric mucosa. The presentation, pathology, management, and a literature review of intussusception in CF are discussed.
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