Peer-reviewed veterinary case report
Acute Ulcerative Enterocolitis With Severe Protein Loss Due to Mucosal Invasion With. in a Dog With Exocrine Pancreatic Insufficiency: A Case Report.
- Journal:
- Frontiers in veterinary science
- Year:
- 2020
- Authors:
- Cartwright, Jennifer A et al.
- Affiliation:
- Queen's Medical Research Institute · United Kingdom
- Species:
- dog
Plain-English summary
A dog with exocrine pancreatic insufficiency (a condition where the pancreas doesn't produce enough enzymes for digestion) developed a serious intestinal problem that caused severe protein loss. The dog showed signs of a systemic inflammatory response, which means its body was reacting strongly to an underlying issue, but the exact cause didn't fit into any common intestinal diseases. After thorough testing, it was found that the dog had inflammation and ulcers in the intestines, along with a resistant bacterial infection. The dog needed intensive care, including special feeding methods, and was treated with antibiotics and steroids. Ultimately, the dog's condition improved and stabilized with this treatment.
Abstract
We describe an unusual case of severe acute protein-losing enteropathy in a dog, which presented with a systemic inflammatory response syndrome. This dog's condition could not be categorized as any well-known canine intestinal condition. Instead, components of several enteropathies like acute hemorrhagic diarrhea syndrome (AHDS), chronic inflammatory enteropathy (CIE), and ulcerative and granulomatous colitis were present. Thorough investigations identified concurrent exocrine pancreatic insufficiency (EPI) and hypocobalaminemia. On histopathology, marked diffuse chronic-active ileitis and ulcerative colitis with fibroplasia and neovascularization were present. Intestinal biopsy cultures identifiedand multiresistant. The latter was identified as mucosally invasive using fluorescenthybridization (FISH). Protracted clinical signs following the acute presentation required intensive care including enteral and parenteral feeding for a successful outcome, but eventually stabilized with antibiotics and immunosuppressive doses of glucocorticoids. This case highlights a potentially previously unrecognized condition, suspected to be a form of CIE manifesting acutely after bacterial mucosal invasion. In this case, this might have been facilitated by EPI-induced dysbiosis. The use of FISH and mucosal culture in this context provided important clinical information and should be considered more frequently in CIE and non-responsive AHDS.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/33195581/