Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps throughout the gastrointestinal tract, mostly causing gastrointestinal bleeding and recurrent intestinal obstructions. Few intussusception related to PJS occurs reportedly in adults. Unlike pedia...

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Autores principales: AlSamman, Mohd Amer, Ferreira, Jason D., Moustafa, Abdelmoniem, Moveson, Jonathan, Akerman, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396794/
https://www.ncbi.nlm.nih.gov/pubmed/30834034
http://dx.doi.org/10.14740/gr1130
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author AlSamman, Mohd Amer
Ferreira, Jason D.
Moustafa, Abdelmoniem
Moveson, Jonathan
Akerman, Paul
author_facet AlSamman, Mohd Amer
Ferreira, Jason D.
Moustafa, Abdelmoniem
Moveson, Jonathan
Akerman, Paul
author_sort AlSamman, Mohd Amer
collection PubMed
description Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps throughout the gastrointestinal tract, mostly causing gastrointestinal bleeding and recurrent intestinal obstructions. Few intussusception related to PJS occurs reportedly in adults. Unlike pediatric cases almost all reported cases end up with surgical resection. Here we present a case of PSJ-related intussusception in an adult patient treated successfully with endoscopic approach, with no surgical intervention required.
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spelling pubmed-63967942019-03-04 Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome AlSamman, Mohd Amer Ferreira, Jason D. Moustafa, Abdelmoniem Moveson, Jonathan Akerman, Paul Gastroenterology Res Case Report Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps throughout the gastrointestinal tract, mostly causing gastrointestinal bleeding and recurrent intestinal obstructions. Few intussusception related to PJS occurs reportedly in adults. Unlike pediatric cases almost all reported cases end up with surgical resection. Here we present a case of PSJ-related intussusception in an adult patient treated successfully with endoscopic approach, with no surgical intervention required. Elmer Press 2019-02 2019-02-26 /pmc/articles/PMC6396794/ /pubmed/30834034 http://dx.doi.org/10.14740/gr1130 Text en Copyright 2019, AlSamman et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
AlSamman, Mohd Amer
Ferreira, Jason D.
Moustafa, Abdelmoniem
Moveson, Jonathan
Akerman, Paul
Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title_full Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title_fullStr Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title_full_unstemmed Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title_short Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
title_sort successful endoscopic reduction of an ileocolonic intussusception in an adult with peutz-jeghers syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396794/
https://www.ncbi.nlm.nih.gov/pubmed/30834034
http://dx.doi.org/10.14740/gr1130
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