Peer-reviewed veterinary case report
Severe ulcerative gut disease with protein loss in a dog
By Cartwright, Jennifer A et al.·Published in Frontiers in veterinary science·2020·Queen's Medical Research Institute, United Kingdom·View original on PubMed →
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Original publication title: Acute Ulcerative Enterocolitis With Severe Protein Loss Due to Mucosal Invasion With. in a Dog With Exocrine Pancreatic Insufficiency: A Case Report.
- Species:
- dog
Plain-English summary
A dog with exocrine pancreatic insufficiency (EPI) developed severe diarrhea and weight loss due to a rare intestinal condition that caused protein loss. The dog showed signs of inflammation and had a bacterial infection that invaded the intestinal lining. After extensive testing, the vet provided intensive care, including special feeding and antibiotics, along with immunosuppressive medication to help manage the inflammation. Thankfully, the dog stabilized and improved with this treatment plan, highlighting the importance of thorough diagnostics in unusual cases.
People also search for: dog diarrhea treatment · exocrine pancreatic insufficiency in dogs · protein-losing enteropathy in dogs
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 on PubMed: https://pubmed.ncbi.nlm.nih.gov/33195581/