<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Benigno L</dc:creator>
  <dc:creator>Lisarelli L</dc:creator>
  <dc:creator>Sortino R</dc:creator>
  <dc:creator>Neuweiler J</dc:creator>
  <dc:creator>Steffen T</dc:creator>
  <dc:date>2020</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Intestinal intussusception is a rare cause of intestinal obstruction; intestinal intussusception associated with endometriosis is very rare. The varied clinical presentations make the diagnosis demanding. In this article, we report the case of a young female patient with an intestinal obstruction due to intussusception. The successive histologic examination of the resected sample showed advanced endometriosis. This is a very rare entity with only a few similar cases reported in the literature.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/139799</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/jscr/rjaa116</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/32595920</dc:relation>
  <dc:source>Journal of surgical case reports. - 2020</dc:source>
  <dc:title xmlns:ns1="xml" ns1:lang="en">A rare case of ileocolic intussusception due to severe endometriosis.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>