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Australian veterinary journal2007; 85(8); 337-340; doi: 10.1111/j.1751-0813.2007.00144.x

Hepatic encephalopathy in a pregnant mare: identification of histopathological changes in the brain of a mare and fetus.

Abstract: An 11-year-old Thoroughbred broodmare was evaluated for suspected hepatic dysfunction. Clinical signs of hepatic encephalopathy were evident at admission. Hepatic ultrasonographic evaluation revealed an increase in hepatic size, rounded borders and normal echogenicity. There was no evidence of cholelithiasis or bile duct distention. Increased activity of hepatic enzymes, increased bile acid and bilirubin concentration and an increased ammonia concentration were supportive of a diagnosis of hepatic disease and hepatic encephalopathy. Histopathological evaluation of a liver biopsy specimen was consistent with chronic active hepatitis. The mare was treated with intravenous fluids and antimicrobials, pentoxyfilline, branched-chain amino acids and dietary manipulation. Clinical improvement was observed initially; however, 3 weeks later, deterioration in the mare's condition necessitated euthanasia. Pathological lesions at necropsy were restricted to the liver and brain. The liver was diffusely firm with a prominent reticular pattern on the cut surface. A large choledocholith was present in the main bile duct of the left liver lobe. Histopathological examination of the liver revealed severe fibrosis, with hyperplastic bile ducts and mononuclear and neutrophilic inflammation. Pathological changes consistent with hepatic encephalopathy, (Alzheimer type II cells), were evident in the cerebrum of both the mare and the fetus.
Publication Date: 2007-08-10 PubMed ID: 17685983DOI: 10.1111/j.1751-0813.2007.00144.xGoogle Scholar: Lookup
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Summary

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The research paper is examining a case of hepatic encephalopathy in a pregnant horse, detailing the symptoms and diagnostic findings, treatments administered, and the eventual deterioration that led to euthanasia, alongside postmortem examinations.

Disease Identification and Assessment

  • This research followed the case of an 11-year-old Thoroughbred broodmare who showed clinical signs of hepatic encephalopathy. Initial assessment included an ultrasonographic evaluation, which revealed changes in the liver such as increased size and rounded borders.
  • No evidence of gallstones (cholelithiasis) or dilatation of the bile duct was presented at this point. In addition to the physical assessment, an increase was noticed in various measures, including the activity of hepatic enzymes, the concentration of bile acid and bilirubin, and the concentration of ammonia. These increases corroborated the suspicion of hepatic disease and hepatic encephalopathy.
  • A liver biopsy led to a histopathological investigation. The results were consistent with chronic active hepatitis, which is a long-term liver inflammation condition.

Treatment and Disease Progression

  • The mare’s treatment included intravenous fluids, antimicrobials, pentoxyfilline (a drug known to increase the flexibility of red blood cells and decrease inflammation), branched-chain amino acids and dietary manipulation.
  • Noticeable improvements were observed initially, however, three weeks later, the mare’s condition deteriorated significantly, ultimately leading to euthanasia.

Postmortem Examination and Findings

  • Necropsy, the postmortem examination of the mare, revealed that disease-related changes were limited to the liver and brain.
  • The liver showed distinctive hardness across its structure, exhibiting a notable reticular pattern on the surface. Additionally, a large gallstone (choledocholith) was identified in the main bile duct of the left liver lobe.
  • Microscopic examination of liver tissue disclosed extensive fibrosis (excessive amounts of connective tissue), increased bile duct growth, and inflammation characterized by mononuclear cells and neutrophils.
  • In both the cerebrum of the mare and her fetus, pathological changes that are consistent with hepatic encephalopathy were observed. This key finding presented as Alzheimer type II cells, demonstrating the impact of the mare’s liver pathology on her brain and her unborn foal’s brain.

Cite This Article

APA
Johns IC, Del Piero F, Wilkins PA. (2007). Hepatic encephalopathy in a pregnant mare: identification of histopathological changes in the brain of a mare and fetus. Aust Vet J, 85(8), 337-340. https://doi.org/10.1111/j.1751-0813.2007.00144.x

Publication

ISSN: 0005-0423
NlmUniqueID: 0370616
Country: England
Language: English
Volume: 85
Issue: 8
Pages: 337-340

Researcher Affiliations

Johns, I C
  • Department of Clinical Studies, University of Pennsylvania, Kennett Square, PA, USA. imogen@vet.upenn.edu
Del Piero, F
    Wilkins, P A

      MeSH Terms

      • Animals
      • Brain / pathology
      • Diagnosis, Differential
      • Fatal Outcome
      • Female
      • Hepatic Encephalopathy / complications
      • Hepatic Encephalopathy / pathology
      • Hepatic Encephalopathy / veterinary
      • Hepatitis, Animal / complications
      • Hepatitis, Animal / diagnosis
      • Hepatitis, Animal / pathology
      • Horse Diseases / diagnosis
      • Horse Diseases / pathology
      • Horses
      • Liver / pathology
      • Pregnancy
      • Pregnancy Complications / diagnosis
      • Pregnancy Complications / pathology
      • Pregnancy Complications / veterinary

      Citations

      This article has been cited 3 times.
      1. Kopecka A, Novotna T, Svobodova Z, Drabkova Z. Senecio ovatus poisoning in a horse - A case report. Vet Med (Praha) 2024 Sep;69(9):329-336.
        doi: 10.17221/37/2024-VETMEDpubmed: 39474359google scholar: lookup
      2. Billingham MJ, Rizk R. Role of early management of hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome in pregnancy. BMJ Case Rep 2021 Jul 1;14(7).
        doi: 10.1136/bcr-2020-241424pubmed: 34210698google scholar: lookup
      3. Hussamy DJ, Nelson DB, Shivvers SA. Hyperammonemia: a report of maternal biliary cirrhosis and neonatal outcome. Case Rep Crit Care 2013;2013:507169.
        doi: 10.1155/2013/507169pubmed: 24829827google scholar: lookup