Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate

Segmental intestinal dilatation (SID) is a rare developmental anomaly of the midgut, characterized by sharply demarcated dilatation of a gastrointestinal segment with clinical findings of intestinal obstruction. Although morphologic criteria for SID are clearly delineated, etiological origin of dila...

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Main Authors:	Soyer, Tutku, Talim, Beril, Tanyel, Feridun Cahit
Format:	Online
Language:	English
Published:	Springer Berlin Heidelberg 2015
Online Access:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747919/

id	pubmed-4747919
recordtype	oai_dc
spelling	pubmed-47479192016-02-19 Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate Soyer, Tutku Talim, Beril Tanyel, Feridun Cahit Case Report Segmental intestinal dilatation (SID) is a rare developmental anomaly of the midgut, characterized by sharply demarcated dilatation of a gastrointestinal segment with clinical findings of intestinal obstruction. Although morphologic criteria for SID are clearly delineated, etiological origin of dilated intestine is unknown. Histology of the resected segment is usually reported to have normal presence of ganglion cells in the myenteric and submucosal plexuses. Intestinal muscle is hypertrophied, and heterotopic gastric mucosa may also be encountered. A 3-day-old male infant presenting with clinical findings of intestinal obstruction was diagnosed to have SID and had supernumerary intestinal muscle coat (SIMC) in the dilated segment, without any evidence of neurological abnormality. Histopathological findings of the resected ileal segment are reported to discuss the role of architectural malformation of muscularis propria as a cause of SID. Springer Berlin Heidelberg 2015-02-17 /pmc/articles/PMC4747919/ /pubmed/26943384 http://dx.doi.org/10.1186/s40792-015-0022-8 Text en © Soyer et al.; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
repository_type	Open Access Journal
institution_category	Foreign Institution
institution	US National Center for Biotechnology Information
building	NCBI PubMed
collection	Online Access
language	English
format	Online
author	Soyer, Tutku Talim, Beril Tanyel, Feridun Cahit
spellingShingle	Soyer, Tutku Talim, Beril Tanyel, Feridun Cahit Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
author_facet	Soyer, Tutku Talim, Beril Tanyel, Feridun Cahit
author_sort	Soyer, Tutku
title	Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
title_short	Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
title_full	Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
title_fullStr	Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
title_full_unstemmed	Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
title_sort	segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate
description	Segmental intestinal dilatation (SID) is a rare developmental anomaly of the midgut, characterized by sharply demarcated dilatation of a gastrointestinal segment with clinical findings of intestinal obstruction. Although morphologic criteria for SID are clearly delineated, etiological origin of dilated intestine is unknown. Histology of the resected segment is usually reported to have normal presence of ganglion cells in the myenteric and submucosal plexuses. Intestinal muscle is hypertrophied, and heterotopic gastric mucosa may also be encountered. A 3-day-old male infant presenting with clinical findings of intestinal obstruction was diagnosed to have SID and had supernumerary intestinal muscle coat (SIMC) in the dilated segment, without any evidence of neurological abnormality. Histopathological findings of the resected ileal segment are reported to discuss the role of architectural malformation of muscularis propria as a cause of SID.
publisher	Springer Berlin Heidelberg
publishDate	2015
url	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747919/
_version_	1613536363814060032

Segmental ileal dilatation with supernumerary intestinal muscle coat in a neonate

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