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Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease
BACKGROUND: The diagnostic gold standard of Hirschsprung’s disease (HD) is based on the histopathological assessment of colorectal biopsies. Although data on cholinergic innervation and ganglion cell (GC) distribution exist, only few studies have examined these two key features together. We assessed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445925/ https://www.ncbi.nlm.nih.gov/pubmed/32838761 http://dx.doi.org/10.1186/s12887-020-02299-z |
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author | Braczynski, Anne K. Gfroerer, Stefan Beschorner, Rudi Harter, Patrick N. Baumgarten, Peter Rolle, Udo Mittelbronn, Michel |
author_facet | Braczynski, Anne K. Gfroerer, Stefan Beschorner, Rudi Harter, Patrick N. Baumgarten, Peter Rolle, Udo Mittelbronn, Michel |
author_sort | Braczynski, Anne K. |
collection | PubMed |
description | BACKGROUND: The diagnostic gold standard of Hirschsprung’s disease (HD) is based on the histopathological assessment of colorectal biopsies. Although data on cholinergic innervation and ganglion cell (GC) distribution exist, only few studies have examined these two key features together. We assessed the pattern of cholinergic innervation and the amount of GCs in colorectal specimens of 14 HD patients. METHODS: We established a semi-quantitative score for cholinergic innervation using acetylcholinesterase (AChE) enzyme histochemistry and quantitatively analyzed the number of GCs via NADH tetrazolium reductase (NADH) enzyme histochemistry. We examined both the entire length of the resected specimens as well as defined areas of the transition zone of both pathological and healthy appearing segment. RESULTS: High AChE score values were associated with absence of GCs, and AChE scores were inversely correlated with the number of GCs. Nevertheless, we observed several cases in which one of the two features revealed a normal distribution pattern, whereas the other still displayed pathological features. CONCLUSIONS: Our data support the need for transmural colon biopsies, to enable the best evaluation of both cholinergic innervation and GCs for a reliable assessment of HD. |
format | Online Article Text |
id | pubmed-7445925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74459252020-08-26 Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease Braczynski, Anne K. Gfroerer, Stefan Beschorner, Rudi Harter, Patrick N. Baumgarten, Peter Rolle, Udo Mittelbronn, Michel BMC Pediatr Research Article BACKGROUND: The diagnostic gold standard of Hirschsprung’s disease (HD) is based on the histopathological assessment of colorectal biopsies. Although data on cholinergic innervation and ganglion cell (GC) distribution exist, only few studies have examined these two key features together. We assessed the pattern of cholinergic innervation and the amount of GCs in colorectal specimens of 14 HD patients. METHODS: We established a semi-quantitative score for cholinergic innervation using acetylcholinesterase (AChE) enzyme histochemistry and quantitatively analyzed the number of GCs via NADH tetrazolium reductase (NADH) enzyme histochemistry. We examined both the entire length of the resected specimens as well as defined areas of the transition zone of both pathological and healthy appearing segment. RESULTS: High AChE score values were associated with absence of GCs, and AChE scores were inversely correlated with the number of GCs. Nevertheless, we observed several cases in which one of the two features revealed a normal distribution pattern, whereas the other still displayed pathological features. CONCLUSIONS: Our data support the need for transmural colon biopsies, to enable the best evaluation of both cholinergic innervation and GCs for a reliable assessment of HD. BioMed Central 2020-08-24 /pmc/articles/PMC7445925/ /pubmed/32838761 http://dx.doi.org/10.1186/s12887-020-02299-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Braczynski, Anne K. Gfroerer, Stefan Beschorner, Rudi Harter, Patrick N. Baumgarten, Peter Rolle, Udo Mittelbronn, Michel Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title | Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title_full | Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title_fullStr | Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title_full_unstemmed | Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title_short | Cholinergic innervation and ganglion cell distribution in Hirschsprung’s disease |
title_sort | cholinergic innervation and ganglion cell distribution in hirschsprung’s disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445925/ https://www.ncbi.nlm.nih.gov/pubmed/32838761 http://dx.doi.org/10.1186/s12887-020-02299-z |
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