Page 727 - Clinical Small Animal Internal Medicine
P. 727

695


  VetBooks.ir






               64

               Canine Inflammatory Liver Disease

               Nick Bexfield, BVetMed, PhD, DSAM, DECVIM-CA, PGDipMEdSci, FHEA, MRCVS
               Department of Veterinary Medicine, Queen’s Veterinary School Hospital, University of Cambridge, Cambridge, UK



               The most frequently identified inflammatory liver dis-  of hepatic fibrosis in dogs. Hepatic stellate cells reside in
               eases in dogs are nonspecific reactive hepatitis, acute   the  space  of  Disse,  between  the  sinusoidal  endothelial
               hepatitis (AH), and chronic hepatitis (CH) and their his-  cells and the hepatocytes. In the healthy liver, they are
               tologic appearance has been standardized by the World   the major storage site of vitamin A, but in chronic liver
               Small Animal Veterinary Association’s (WSAVA) Liver   injury they are stimulated to transform into collagen‐
               Standardization Group. Nonspecific reactive hepatitis   secreting, activated cells that express smooth muscle‐
               represents a nonspecific response to a variety of extrahe-  specific alpha‐actin and secrete high‐density matrix and
               patic disease processes, especially febrile illnesses and   collagen into the space of Disse. The secretion of colla-
               inflammation somewhere in the splanchnic bed.      gen  and formation  of  fibrous  tissue  from  activated
               Histologically, it is characterized by an inflammatory     stellate cells are believed to be indirect via the release
               infiltrate in portal areas, and sometimes in the paren-  of  cytokines from inflammatory cells, although some
               chyma, without  evidence of hepatocellular necrosis or   inflammatory mediators  act on  them directly. Fibrous
               apoptosis. It results from a disease occurring outside the   tissue within the liver leads to the development of intra-
               liver, so will not be discussed further. AH is characterized   hepatic portal hypertension by altering sinusoidal tone
               by a combination of inflammation and hepatocellular   and blood flow. The development of portal hypertension
               apoptosis and necrosis, with the specific features varying   results in many of the complications of chronic liver dis-
               according to the cause. The majority of AH cases occur as   ease such as ascites and gastrointestinal (GI) ulceration.
               a result of toxin or drug ingestion, and are discussed fur-  The known or postulated causes of CH are listed below,
               ther in Chapter 62.                                although the majority of cases have no identifiable cause
                 Acute hepatitis can sometimes be caused by infection   and thus are termed idiopathic.
               with certain bacteria or viruses, and these are detailed
               below. CH is defined histologically by the presence of
               hepatocellular apoptosis or necrosis, a variable mononu-  Infectious Causes
               clear or mixed inflammatory cell infiltrate, regeneration,   Canine Acidophil Cell Hepatitis Virus
               and fibrosis. It is the most frequently identified canine   A potential viral cause of AH and CH was identified in
               inflammatory liver disease and so will be the focus of most   1985 and named “canine acidophil cell hepatitis virus”
               of this chapter.                                   although no specific agent was isolated. Histopathologic
                                                                  examination revealed an inflammatory infiltrate with
                 Chronic Hepatitis                                areas of hepatocyte necrosis and scattered numbers of
                                                                  large cells with acidophilic cytoplasm, termed “acido-
                                                                  phil cells.” When liver homogenate and serum from
               Etiology/Pathophysiology
                                                                  affected dogs were injected into naive animals, this
               The development of fibrosis is the key pathologic change   resulted in the development of clinical and pathologic
               that leads to the development of CH. The hepatic stellate   changes of AH that in some dogs progressed to CH.
               cell, also known as the Ito cell or lipocyte, is central in the   However, no further work to identify the potential
               development of  fibrosis in  humans  and  rats, and  evi-  transmissible hepatitis‐causing agent was performed,
               dence also suggests its involvement in the pathogenesis   nor have further reports emerged.


               Clinical Small Animal Internal Medicine Volume I, First Edition. Edited by David S. Bruyette.
               © 2020 John Wiley & Sons, Inc. Published 2020 by John Wiley & Sons, Inc.
               Companion website: www.wiley.com/go/bruyette/clinical
   722   723   724   725   726   727   728   729   730   731   732