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Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review

Diffuse ganglioneuromatosis (DG) of the gastrointestinal tract is a rare condition that is closely associated with neurofibromatosis type 1 and multiple endocrine neoplasia type 2B. The occurrence of DG with multiple schwannomas, which, of the GI tract, usually affect the stomach, is considerably mo...

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Autores principales: LU, CHANGLI, QIU, YAN, LU, XUFENG, LI, GANDI, BU, HONG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316863/
https://www.ncbi.nlm.nih.gov/pubmed/25667620
http://dx.doi.org/10.3892/etm.2015.2212
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author LU, CHANGLI
QIU, YAN
LU, XUFENG
LI, GANDI
BU, HONG
author_facet LU, CHANGLI
QIU, YAN
LU, XUFENG
LI, GANDI
BU, HONG
author_sort LU, CHANGLI
collection PubMed
description Diffuse ganglioneuromatosis (DG) of the gastrointestinal tract is a rare condition that is closely associated with neurofibromatosis type 1 and multiple endocrine neoplasia type 2B. The occurrence of DG with multiple schwannomas, which, of the GI tract, usually affect the stomach, is considerably more rare. The present study describes the case of a 54-year-old male with indolent DG, principally involving the small intestine and colon, associated with multiple schwannomas in the subserosa. The patient was treated with surgery. A brief overview of intestinal ganglioneuromatous lesions and the associated conditions is additionally presented.
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spelling pubmed-43168632015-02-09 Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review LU, CHANGLI QIU, YAN LU, XUFENG LI, GANDI BU, HONG Exp Ther Med Articles Diffuse ganglioneuromatosis (DG) of the gastrointestinal tract is a rare condition that is closely associated with neurofibromatosis type 1 and multiple endocrine neoplasia type 2B. The occurrence of DG with multiple schwannomas, which, of the GI tract, usually affect the stomach, is considerably more rare. The present study describes the case of a 54-year-old male with indolent DG, principally involving the small intestine and colon, associated with multiple schwannomas in the subserosa. The patient was treated with surgery. A brief overview of intestinal ganglioneuromatous lesions and the associated conditions is additionally presented. D.A. Spandidos 2015-03 2015-01-23 /pmc/articles/PMC4316863/ /pubmed/25667620 http://dx.doi.org/10.3892/etm.2015.2212 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LU, CHANGLI
QIU, YAN
LU, XUFENG
LI, GANDI
BU, HONG
Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title_full Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title_fullStr Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title_full_unstemmed Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title_short Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
title_sort synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: a case report and literature review
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316863/
https://www.ncbi.nlm.nih.gov/pubmed/25667620
http://dx.doi.org/10.3892/etm.2015.2212
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