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Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa
AIMS: Studying crypt branching in ulcerative colitis (UC) and in infectious colitis (IC), we detected previously unreported crypt-associated anomalies (CAAs). The objective was to describe, illustrate and assess the frequency of CAAs in inflamed colon mucosa in patients with UC and IC. METHODS: Sect...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423556/ https://www.ncbi.nlm.nih.gov/pubmed/35273118 http://dx.doi.org/10.1136/jclinpath-2022-208152 |
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author | Rubio, Carlos A Vieth, Michael Lang-Schwarz, Corinna |
author_facet | Rubio, Carlos A Vieth, Michael Lang-Schwarz, Corinna |
author_sort | Rubio, Carlos A |
collection | PubMed |
description | AIMS: Studying crypt branching in ulcerative colitis (UC) and in infectious colitis (IC), we detected previously unreported crypt-associated anomalies (CAAs). The objective was to describe, illustrate and assess the frequency of CAAs in inflamed colon mucosa in patients with UC and IC. METHODS: Sections from 100 consecutive biopsies with UC, in 50 with IC and in 27 with UC in remission (UCR) were reviewed. The following CAAs were identified: crypt eosinophilia, intracryptal epithelial hyperplasia, intracryptal epithelial budding, intracryptal supernumerary crypts, intracryptal epithelial bridges, crypt rings in rows and off-centre epithelial budding. RESULTS: The frequency of crypts with extensive crypt eosinophilia and with intracryptal epithelial budding was significantly higher in UC than in IC and UCR (p<0.05); the frequency in the remaining histological parameters was similar in UC, IC and UCR. CONCLUSIONS: CAAs were found interspersed with branching crypts. CAAs persisted in long-lasting UC mucosal inflammation, but declined when the inflammation waned. Since similar anomalies are not present in normal colon mucosa, the results suggest that CAAs had been boosted by the ongoing mucosal inflammation. The development of these previously unreported CAAs in the colon mucosa with inflammation might embody pathological aberrations of cryptogenesis. |
format | Online Article Text |
id | pubmed-10423556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-104235562023-08-14 Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa Rubio, Carlos A Vieth, Michael Lang-Schwarz, Corinna J Clin Pathol Original Research AIMS: Studying crypt branching in ulcerative colitis (UC) and in infectious colitis (IC), we detected previously unreported crypt-associated anomalies (CAAs). The objective was to describe, illustrate and assess the frequency of CAAs in inflamed colon mucosa in patients with UC and IC. METHODS: Sections from 100 consecutive biopsies with UC, in 50 with IC and in 27 with UC in remission (UCR) were reviewed. The following CAAs were identified: crypt eosinophilia, intracryptal epithelial hyperplasia, intracryptal epithelial budding, intracryptal supernumerary crypts, intracryptal epithelial bridges, crypt rings in rows and off-centre epithelial budding. RESULTS: The frequency of crypts with extensive crypt eosinophilia and with intracryptal epithelial budding was significantly higher in UC than in IC and UCR (p<0.05); the frequency in the remaining histological parameters was similar in UC, IC and UCR. CONCLUSIONS: CAAs were found interspersed with branching crypts. CAAs persisted in long-lasting UC mucosal inflammation, but declined when the inflammation waned. Since similar anomalies are not present in normal colon mucosa, the results suggest that CAAs had been boosted by the ongoing mucosal inflammation. The development of these previously unreported CAAs in the colon mucosa with inflammation might embody pathological aberrations of cryptogenesis. BMJ Publishing Group 2023-08 2022-03-10 /pmc/articles/PMC10423556/ /pubmed/35273118 http://dx.doi.org/10.1136/jclinpath-2022-208152 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Research Rubio, Carlos A Vieth, Michael Lang-Schwarz, Corinna Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title | Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title_full | Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title_fullStr | Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title_full_unstemmed | Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title_short | Novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
title_sort | novel histological repertoire of crypt-associated anomalies in inflamed colon mucosa |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423556/ https://www.ncbi.nlm.nih.gov/pubmed/35273118 http://dx.doi.org/10.1136/jclinpath-2022-208152 |
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