Page 639 - Small Animal Internal Medicine, 6th Edition
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CHAPTER 36   Hepatobiliary Diseases in the Dog   611


            of them. Symptomatic therapy for HE, ascites, and GI ulcer-  and anecdotally in other breeds. Pillai et al. in 2016 reported
            ation (if present) is usually successful (see earlier). It should   30 Boxer dogs with ductal plate malformations, suggesting
  VetBooks.ir  be noted that glucocorticoid therapy is absolutely contrain-  an increased prevalence in this breed. Interestingly, there was
                                                                 a high prevalence of concurrent congenital hepatic abnor-
            dicated in these dogs and is likely to worsen the outcome
            because of the associated portal hypertension and high risk
                                                                 cular abnormalities. Two dogs also had Caroli’s disease.
            of GI ulceration. This underlines the importance of liver   malities such as atrophy of liver lobes or gallbladder or vas-
            biopsy in these dogs, allowing differentiation from chronic   Recent work at the University of Cambridge in the UK sug-
            hepatitis.                                           gests that Skye Terrier hepatitis may in fact also be a con-
              One study of dogs with noncirrhotic portal hypertension   genital ductal plate abnormality.
            concluded that affected dogs might live as long as 9 years
            after diagnosis with appropriate symptomatic therapy (Bunch   Clinical Features
            et al., 2001). A few dogs were euthanized because of prob-  Dogs with congenital hepatic fibrosis usually present at a
            lems related to persistent portal hypertension (e.g., duodenal   young age, with most being under 1 year of age at presenta-
            ulceration). Dogs with MVD tend to have milder clinical   tion, but occasionally dogs present as old as 10 years of age.
            signs than dogs with congenital PSSs and can be managed   Clinical signs are typical of portal hypertension (see earlier)
            medically with success over the long term. Affected dogs   including ascites, vomiting, and diarrhea, and also in some
            seem to live comfortably, in good to excellent condition, for   cases melena. Some dogs present with HE.
            at least 5 years.
                                                                 Diagnosis
            Congenital Ductal Plate Abnormalities                Clinicopathologic abnormalities are very similar to chronic
                                                                 liver  disease.  Affected  dogs  usually  have  elevated  liver
            Etiology                                             enzymes  but  very  rarely elevated bilirubin.  Bile  acids  are
            Ductal plate abnormalities are congenital diseases of the liver   often elevated, associated with development of acquired
            causes by abnormalities in development of the ductal plate   PSSs. Some dogs have microcytic red cells. Diagnostic
            (see later). There are a variety of phenotypes depending on   imaging findings are generally indistinguishable from cir-
            the stage in embryologic development when the abnormality   rhosis: dogs usually have a small hyperechoic liver and free
            occurs,  and  there  may be  some  overlap  with  portal  vein   abdominal  fluid. Some cases may  have  other congenital
            abnormalities. Traditionally, these conditions were consid-  abnormalities such as atresia of the gallbladder or a liver
            ered rare in dogs, but with increasing awareness of the condi-  lobe, or large liver cysts that would increase the index of
            tion, more cases are being identified. The commonest   suspicion of ductal plate abnormality. However, confirma-
            phenotypes in dogs are Caroli’s disease, where bile ducts are   tion of diagnosis requires a liver biopsy. Congenital hepatic
            large, and cystic and congenital hepatic fibrosis, where there   fibrosis typically appears as abnormal, expanded portal
            are multiple small bile ductules and associated fibrosis. The   tracts  with  multiple  small  bile  duct  profiles  and  bands  of
            latter can be confused with cirrhosis on pathology and hence   fibrosis both periportally and extending into the liver. These
            potential underdiagnosis. The differentiation is important   tracts of fibrosis can sometimes resemble lobular dissecting
            because dogs with congenital hepatic fibrosis generally have   hepatitis. There may also be areas of fibrosis and multiple
            a better prognosis than those with cirrhosis if appropriately   small bile ducts underneath the liver capsule, similar to Mey-
            treated.                                             enburg complexes reported in humans. Bile ducts typically
              The ductal plate is the embryonic precursor of the inter-  have cuboidal rather than columnar epithelium. Increased
            lobular and intralobular bile ducts. It is a double layer of   copper accumulation is common in affected boxers and Skye
            embryonic epithelium surrounding the portal veins. Bile   Terriers, and is assumed to be secondary to abnormal excre-
            duct development involves many signaling molecules, and   tion.  The disease is  often  patchy  affecting  individual liver
            abnormalities in this development result in a wide variety of   lobes more than others.
            presentations in human medicine, with persistence of
            embryonic bile ducts and varying amounts of periportal   Treatment and Prognosis
            fibrosis. The drivers of fibrosis in this context remain incom-  Treatment of affected animals is symptomatic because
            pletely understood. There are a variety of genetic mutations   there is no cure for the congenital abnormality. Nonethe-
            involved in humans, many of them autosomal dominant, and   less, many dogs have a good long-term prognosis with
            affected individuals may have concurrent renal cysts or skel-  supportive care; a reported median survival in one study
            etal abnormalities. The disease phenotype in the liver   in Boxers was 8.8 years in dogs without acquired PSS and
            depends on which bile ducts are affected; maturation arrest   7.5 years in dogs with PSS. Anecdotally, Skye Terriers and
            of small interlobular bile ducts results in congenital hepatic   other breeds can also do well long term. Management is
            fibrosis, whereas maturation arrest of medium intrahepatic   the same as for dogs with portal hypertension, with symp-
            bile ducts results in Caroli’s disease. The genetics of ductal   tomatic treatment of ascites with spironolactone and careful
            plate anomalies are currently unknown in dogs. The first   dietary and other management for HE (see Box 36.6). It is
            report of congenital hepatic fibrosis in dogs in the veterinary   particularly important that affected dogs are fed sufficient
            literature was in 2010 (Brown et al., 2010). Since that time,   dietary protein for maintenance because long-term survival
            cases have been reported in Boxer dogs and Skye Terriers   is anticipated.
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