ArticleVeterinary sciences2022
Feline Gastrointestinal Eosinophilic Sclerosing Fibroplasia-Extracellular Matrix Proteins and TGF-β1 Immunoexpression.
Article in Veterinary sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 9 citations in OpenAlex.
- Morphological and Molecular Identification ofPathogens (Basel, Switzerland) · 2026Article
- Obstructive colonic FGESF associated with feline infectious peritonitis in a cat: a case report.BMC veterinary research · 2026Article
- What's your diagnosis? Circumferential small intestinal mass in a cat.Veterinary clinical pathology · 2025Article
- Feline gastrointestinal eosinophilic sclerosing fibroplasia in a young ragdoll cat: with surgical management.Veterinary research communications · 2025Article
- Feline eosinophilic sclerosing fibroplasia associated with T-/natural killer-cell lymphoma.Veterinary pathology · 2025Article
- Feline gastrointestinal eosinophilic sclerosing fibroplasia in two cats: Serial ultrasonographic and computed tomography findings.Veterinarni medicina · 2024Article
- Clinicopathological findings, treatment, and outcome in 60 cats with gastrointestinal eosinophilic sclerosing fibroplasia.Journal of veterinary internal medicineArticle
- Bicavitary involvement of feline eosinophilic sclerosing fibroplasia with intralesional methicillin-resistantJFMS open reportsArticle
- Intrathoracic eosinophilic sclerosing fibroplasia with intralesional bacteria in a cat.JFMS open reportsArticle
- Characterization of intestinal fibrosis in cats with chronic inflammatory enteropathy.Journal of veterinary internal medicineArticle
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Feline gastrointestinal eosinophilic sclerosing fibroplasia (FGESF) has been described as an inflammatory disorder with an eosinophilic component with etiopathogenesis that is still unknown. Sixteen intestinal samples from two veterinary diagnostic services (2014-2017) were included in the study. A histopathological criterion classified the cases into three grades (mild, moderate, and severe) according to the distribution of the lesions and the course. An immunohistochemical study of collagen I, collagen III, fibronectin, and transforming growth factor β1 (TGF-β1) was performed in each case. An immunohistochemical study of mild grades shows greater collagen III immunoexpression, compared to collagen I and fibronectin, which suggests an "early" stage of fibrosis. In more intense grades, an increased immunoexpression of collagen I, compared to collagen III, suggests a "late" stage of fibrosis. Otherwise, the highest expression of TGF-β1 was observed in the moderate phase, due to the high proliferation of reactive fibroblast and intense inflammation. The results suggest that the inflammatory infiltrate is the trigger for the elevation in TGF-β1, altering the collagen type III:I ratio. In conclusion, immunohistochemical studies can be a very useful method in diagnosing cases of FGESF of mild grades and could help to apply a differential diagnosis regarding feline eosinophilic chronic enteritis (CEE) in the context of inflammatory bowel disease (IBD).
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