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Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells

Intestinal neuronal dysplasia type B (IND-B) is a controversial condition among gastrointestinal neuromuscular disorders. Constipation is its most common clinical manifestation in patients. Despite intense scientific research, there are still knowledge gaps regarding the diagnostic criteria for IND-...

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Autores principales: Terra, Simone Antunes, Gonçalves, Anderson Cesar, Lourenção, Pedro Luiz Toledo de Arruda, Rodrigues, Maria Aparecida Marchesan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641051/
https://www.ncbi.nlm.nih.gov/pubmed/34908804
http://dx.doi.org/10.3748/wjg.v27.i44.7649
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author Terra, Simone Antunes
Gonçalves, Anderson Cesar
Lourenção, Pedro Luiz Toledo de Arruda
Rodrigues, Maria Aparecida Marchesan
author_facet Terra, Simone Antunes
Gonçalves, Anderson Cesar
Lourenção, Pedro Luiz Toledo de Arruda
Rodrigues, Maria Aparecida Marchesan
author_sort Terra, Simone Antunes
collection PubMed
description Intestinal neuronal dysplasia type B (IND-B) is a controversial condition among gastrointestinal neuromuscular disorders. Constipation is its most common clinical manifestation in patients. Despite intense scientific research, there are still knowledge gaps regarding the diagnostic criteria for IND-B in the histopathological analysis of rectal biopsies. The guidelines published in the past three decades have directed diagnostic criteria for quantifying the number of ganglion cells in the nervous plexus of the enteric nervous system. However, it is very complex to distinguish numerically what is pathological from what is normal, mainly because of the difficulty in determining a reliable control group composed of healthy children without intestinal symptoms. Thus, a series of immunohistochemical markers have been proposed to assist in the histopathological analysis of the enteric nervous system. Several of these markers facilitate the identification of other structures of the enteric nervous system, in addition to ganglion cells. These structures may be related to the etiopathogenesis of IND-B and represent new possibilities for the histopathological diagnosis of this disease, providing a view beyond the number of ganglion cells. This review critically discusses the aspects related to the disease definitions and diagnostic criteria of this organic cause of constipation.
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spelling pubmed-86410512021-12-13 Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells Terra, Simone Antunes Gonçalves, Anderson Cesar Lourenção, Pedro Luiz Toledo de Arruda Rodrigues, Maria Aparecida Marchesan World J Gastroenterol Minireviews Intestinal neuronal dysplasia type B (IND-B) is a controversial condition among gastrointestinal neuromuscular disorders. Constipation is its most common clinical manifestation in patients. Despite intense scientific research, there are still knowledge gaps regarding the diagnostic criteria for IND-B in the histopathological analysis of rectal biopsies. The guidelines published in the past three decades have directed diagnostic criteria for quantifying the number of ganglion cells in the nervous plexus of the enteric nervous system. However, it is very complex to distinguish numerically what is pathological from what is normal, mainly because of the difficulty in determining a reliable control group composed of healthy children without intestinal symptoms. Thus, a series of immunohistochemical markers have been proposed to assist in the histopathological analysis of the enteric nervous system. Several of these markers facilitate the identification of other structures of the enteric nervous system, in addition to ganglion cells. These structures may be related to the etiopathogenesis of IND-B and represent new possibilities for the histopathological diagnosis of this disease, providing a view beyond the number of ganglion cells. This review critically discusses the aspects related to the disease definitions and diagnostic criteria of this organic cause of constipation. Baishideng Publishing Group Inc 2021-11-28 2021-11-28 /pmc/articles/PMC8641051/ /pubmed/34908804 http://dx.doi.org/10.3748/wjg.v27.i44.7649 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Minireviews
Terra, Simone Antunes
Gonçalves, Anderson Cesar
Lourenção, Pedro Luiz Toledo de Arruda
Rodrigues, Maria Aparecida Marchesan
Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title_full Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title_fullStr Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title_full_unstemmed Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title_short Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells
title_sort challenges in the diagnosis of intestinal neuronal dysplasia type b: a look beyond the number of ganglion cells
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641051/
https://www.ncbi.nlm.nih.gov/pubmed/34908804
http://dx.doi.org/10.3748/wjg.v27.i44.7649
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