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Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report
BACKGROUND: Adult intestinal intussusception is a rare condition caused by the mechanical disruption of bowel motility. A bezoar is defined as indigestible material inside the gastrointestinal tract that develops into a trapped mass; the most frequent bezoar is a trichobezoar. When a trichobezoar ex...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284286/ https://www.ncbi.nlm.nih.gov/pubmed/30522519 http://dx.doi.org/10.1186/s13256-018-1883-9 |
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author | Bolívar-Rodríguez, Martín Adrián Fierro-López, Rodolfo Pamanes-Lozano, Adrián Cazarez-Aguilar, Marcel Antonio Osuna-Wong, Benny Alonso Ortiz-Bojórquez, José Cándido |
author_facet | Bolívar-Rodríguez, Martín Adrián Fierro-López, Rodolfo Pamanes-Lozano, Adrián Cazarez-Aguilar, Marcel Antonio Osuna-Wong, Benny Alonso Ortiz-Bojórquez, José Cándido |
author_sort | Bolívar-Rodríguez, Martín Adrián |
collection | PubMed |
description | BACKGROUND: Adult intestinal intussusception is a rare condition caused by the mechanical disruption of bowel motility. A bezoar is defined as indigestible material inside the gastrointestinal tract that develops into a trapped mass; the most frequent bezoar is a trichobezoar. When a trichobezoar extends into the small intestine it is defined as Rapunzel’s syndrome. Literature describing complications related to this pathology remains scarce. CASE PRESENTATION: A 16-year-old Mexican girl presented to our emergency room with acute abdomen and a presumptive diagnosis of intestinal obstruction. Computed tomography was suggestive of intussusception. Surgery confirmed a jejunal-jejunal intussusception with a mass within the gastric cavity extending into her small intestine, corresponding to a trichobezoar. A manual intussusception reduction and a gastrotomy with extraction of the trichobezoar were performed. CONCLUSIONS: We present a case of a jejunum intussusception as a complication of Rapunzel syndrome. Our patient had a favorable outcome after surgical intervention with a manual intussusception reduction, with retrograde displacement of the trichobezoar into the gastric lumen, and a complete extraction through a gastrostomy. Follow-up included psychiatric evaluation. |
format | Online Article Text |
id | pubmed-6284286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62842862018-12-14 Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report Bolívar-Rodríguez, Martín Adrián Fierro-López, Rodolfo Pamanes-Lozano, Adrián Cazarez-Aguilar, Marcel Antonio Osuna-Wong, Benny Alonso Ortiz-Bojórquez, José Cándido J Med Case Rep Case Report BACKGROUND: Adult intestinal intussusception is a rare condition caused by the mechanical disruption of bowel motility. A bezoar is defined as indigestible material inside the gastrointestinal tract that develops into a trapped mass; the most frequent bezoar is a trichobezoar. When a trichobezoar extends into the small intestine it is defined as Rapunzel’s syndrome. Literature describing complications related to this pathology remains scarce. CASE PRESENTATION: A 16-year-old Mexican girl presented to our emergency room with acute abdomen and a presumptive diagnosis of intestinal obstruction. Computed tomography was suggestive of intussusception. Surgery confirmed a jejunal-jejunal intussusception with a mass within the gastric cavity extending into her small intestine, corresponding to a trichobezoar. A manual intussusception reduction and a gastrotomy with extraction of the trichobezoar were performed. CONCLUSIONS: We present a case of a jejunum intussusception as a complication of Rapunzel syndrome. Our patient had a favorable outcome after surgical intervention with a manual intussusception reduction, with retrograde displacement of the trichobezoar into the gastric lumen, and a complete extraction through a gastrostomy. Follow-up included psychiatric evaluation. BioMed Central 2018-12-07 /pmc/articles/PMC6284286/ /pubmed/30522519 http://dx.doi.org/10.1186/s13256-018-1883-9 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Bolívar-Rodríguez, Martín Adrián Fierro-López, Rodolfo Pamanes-Lozano, Adrián Cazarez-Aguilar, Marcel Antonio Osuna-Wong, Benny Alonso Ortiz-Bojórquez, José Cándido Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title | Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title_full | Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title_fullStr | Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title_full_unstemmed | Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title_short | Surgical outcome of jejunum-jejunum intussusception secondary to Rapunzel syndrome: a case report |
title_sort | surgical outcome of jejunum-jejunum intussusception secondary to rapunzel syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284286/ https://www.ncbi.nlm.nih.gov/pubmed/30522519 http://dx.doi.org/10.1186/s13256-018-1883-9 |
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