| Literature DB >> 32595920 |
Luca Benigno1, Loriana Lisarelli1, Rosita Sortino1, Joerg Neuweiler2, Thomas Steffen1.
Abstract
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. Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved.Entities:
Year: 2020 PMID: 32595920 PMCID: PMC7303101 DOI: 10.1093/jscr/rjaa116
Source DB: PubMed Journal: J Surg Case Rep ISSN: 2042-8812
Figure 1Ultrasonography with a circular concentric layer highly suspicious of invagination.
Figure 2CT scan with long ileocolonic intussusception of the ascending colon into the transverse colon, with possible involvement of the terminal ileum, coronal plane.
Figure 3CT scan with long ileocolonic intussusception of the ascending colon into the transverse colon, with possible involvement of the terminal ileum, axial plane (white arrow).
Figure 4Ileocolic specimen with endometriosis node as the cause of the intussusception.
Figure 5Histological specimen of the endometriosis (scale 200 μm). In detail the outer layer of the muscular bowel wall and adjacent subserosal tissue with fibrosis; embedded there are islands of inconspicuous endometrial-type glands and stroma (black star) with banal cytology.