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Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy

BACKGROUND: Intestinal fibrosis (IF) is commonly identified on histopathology of intestinal biopsy specimens (IBSp) from cats with chronic inflammatory enteropathy (CIE) however, its clinical relevance is unknown. OBJECTIVES: Characterize and determine the clinical relevance of IF in cats with CIE....

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Autores principales: Bandara, Yuvani, Priestnall, Simon L., Chang, Yu‐Mei, Kathrani, Aarti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229354/
https://www.ncbi.nlm.nih.gov/pubmed/37052621
http://dx.doi.org/10.1111/jvim.16688
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author Bandara, Yuvani
Priestnall, Simon L.
Chang, Yu‐Mei
Kathrani, Aarti
author_facet Bandara, Yuvani
Priestnall, Simon L.
Chang, Yu‐Mei
Kathrani, Aarti
author_sort Bandara, Yuvani
collection PubMed
description BACKGROUND: Intestinal fibrosis (IF) is commonly identified on histopathology of intestinal biopsy specimens (IBSp) from cats with chronic inflammatory enteropathy (CIE) however, its clinical relevance is unknown. OBJECTIVES: Characterize and determine the clinical relevance of IF in cats with CIE. ANIMALS: Sixty‐five client‐owned cats diagnosed with CIE after gastrointestinal histopathology from a single referral hospital in the United Kingdom. METHODS: Medical records were retrospectively searched for cases of CIE on the basis of histopathology of IBSp. The IBSp from eligible cats were re‐reviewed by a single board‐certified veterinary pathologist for inclusion. Masson's trichrome (MT) stain and immunohistochemical labeling using antivimentin and anticollagen I antibodies to identify IF. For each case, various variables at the time of diagnostic investigation were recorded and referring veterinarians were contacted for follow‐up information. RESULTS: Mucosal fibrosis was identified in 51% of duodenal and 76% of colonic hematoxylin and eosin (HE)‐stained IBSp. Vimentin labeling and MT staining identified additional cases of IF in 65% and 58% of the duodenal biopsy specimens, respectively. Vimentin labeling detected IF in 79% of the colonic biopsy specimens. Positive vimentin labeling and MT staining of the colonic mucosa were associated with decreased likelihood of attaining clinical remission and increased risk of death because of CIE (P < .05). CONCLUSIONS AND CLINICAL IMPORTANCE: Additional stains at initial histopathologic examination of IBSp allow for better identification of IF compared to routine HE staining. Identification of IF in colonic biopsy specimens by vimentin immunolabeling and MT staining may provide prognostic information in cats with CIE.
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spelling pubmed-102293542023-06-01 Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy Bandara, Yuvani Priestnall, Simon L. Chang, Yu‐Mei Kathrani, Aarti J Vet Intern Med SMALL ANIMAL BACKGROUND: Intestinal fibrosis (IF) is commonly identified on histopathology of intestinal biopsy specimens (IBSp) from cats with chronic inflammatory enteropathy (CIE) however, its clinical relevance is unknown. OBJECTIVES: Characterize and determine the clinical relevance of IF in cats with CIE. ANIMALS: Sixty‐five client‐owned cats diagnosed with CIE after gastrointestinal histopathology from a single referral hospital in the United Kingdom. METHODS: Medical records were retrospectively searched for cases of CIE on the basis of histopathology of IBSp. The IBSp from eligible cats were re‐reviewed by a single board‐certified veterinary pathologist for inclusion. Masson's trichrome (MT) stain and immunohistochemical labeling using antivimentin and anticollagen I antibodies to identify IF. For each case, various variables at the time of diagnostic investigation were recorded and referring veterinarians were contacted for follow‐up information. RESULTS: Mucosal fibrosis was identified in 51% of duodenal and 76% of colonic hematoxylin and eosin (HE)‐stained IBSp. Vimentin labeling and MT staining identified additional cases of IF in 65% and 58% of the duodenal biopsy specimens, respectively. Vimentin labeling detected IF in 79% of the colonic biopsy specimens. Positive vimentin labeling and MT staining of the colonic mucosa were associated with decreased likelihood of attaining clinical remission and increased risk of death because of CIE (P < .05). CONCLUSIONS AND CLINICAL IMPORTANCE: Additional stains at initial histopathologic examination of IBSp allow for better identification of IF compared to routine HE staining. Identification of IF in colonic biopsy specimens by vimentin immunolabeling and MT staining may provide prognostic information in cats with CIE. John Wiley & Sons, Inc. 2023-04-13 /pmc/articles/PMC10229354/ /pubmed/37052621 http://dx.doi.org/10.1111/jvim.16688 Text en © 2023 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle SMALL ANIMAL
Bandara, Yuvani
Priestnall, Simon L.
Chang, Yu‐Mei
Kathrani, Aarti
Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title_full Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title_fullStr Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title_full_unstemmed Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title_short Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
title_sort characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229354/
https://www.ncbi.nlm.nih.gov/pubmed/37052621
http://dx.doi.org/10.1111/jvim.16688
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