Page 521 - Small Animal Internal Medicine, 6th Edition
P. 521

CHAPTER 31   Disorders of the Intestinal Tract   493


            attain remission). If these therapeutic trials fail, the next step   lymphocytic lymphoma from severe LPE, even with full-
            may be further therapeutic trials (e.g., fecal transplantation,   thickness tissue samples. Animals with intense dietary reac-
  VetBooks.ir  probiotics), or perhaps biopsy (which should be done before   tions rarely have biopsy findings that resemble lymphoma. If
                                                                 the tissue specimens are of poor quality (i.e., small size,
            administering antiinflammatory or immunosuppressive
                                                                 excessive artifact), it is easy to mistakenly diagnose lym-
            drugs).
                                                                 phoma as LPE. Biopsy of more than one intestinal site (e.g.,
                                                                 duodenum and ileum, as opposed to just duodenum) is
            SMALL INTESTINAL “INFLAMMATORY                       sometimes critical in finding inflammatory and neoplastic
            BOWEL DISEASE” (CHRONIC                              changes. Diagnosis of feline LPE is similar to that of canine
            ENTEROPATHY)                                         LPE. Many cats with IBD have mild to moderate mesenteric
                                                                 lymphadenopathy, which ultrasonographically mimics lym-
            Clinical Features                                    phoma. Cats symptomatic with severe IBD should be evalu-
            Contrary to human medicine, there is not a uniformly   ated for the presence of “triaditis” (i.e., simultaneous
            accepted definition of the term inflammatory bowel disease   inflammation of the intestines, pancreas, and liver).
            (IBD) in veterinary medicine. Some have suggested the term   Diagnosis of EGE is similar to diagnosis of LPE. Dogs
            chronic enteropathy (CE) as an alternative. In this text, IBD   with EGE may have eosinophilia and/or concurrent eosino-
            is defined as an idiopathic inflammation affecting any portion   philic respiratory or cutaneous dietary allergies with pruri-
            of the canine or feline small or large intestine. The cause is   tus. German Shepherds seem overrepresented. Diagnosis of
            believed to involve an inappropriate response by the intesti-  feline EGE centers on finding intestinal eosinophilic infil-
            nal immune system to bacterial and/or dietary antigens that   trates, but splenic, hepatic, lymph node, and bone marrow
            evolves into a self-perpetuating state of inflammation.   infiltrates and peripheral eosinophilia are common.
            Lymphocytic-plasmacytic enteritis (LPE) is the most com-
            monly diagnosed form of canine and feline IBD. Chronic   Treatment
            small intestinal diarrhea is common, but patients can have   “Mild” LPE is typically dietary-responsive or ARE that was
            weight loss despite normal stools. If the duodenum is severely   not diagnosed before biopsy. Severe LPE is usually dietary-
            affected, vomiting may be the major sign. PLE can occur   and/or antibiotic-responsive enteropathy that has become
            with the more severe forms. The clinical and histologic fea-  self-perpetuating such that antiinflammatory therapy is
            tures of IBD can closely resemble those of alimentary lym-  necessary.  It  is  often  important  to  co-administer  dietary
            phoma (see  pp. 502-503), especially well-differentiated,   and  antimicrobial  therapy  along  with  antiinflammatory/
            small cell alimentary lymphoma in cats.              immunosuppressive therapy. Prednisolone (2.2 mg/kg/
              Eosinophilic gastroenterocolitis (EGE) is usually an aller-  day PO) is typically first-line therapy in these patients. If
            gic reaction to dietary substances (e.g., beef, milk). Clinical   a patient responds to prednisolone but cannot tolerate the
            signs usually but not always respond to dietary change, and   steroid side effects, then budesonide may be considered.
            glucocorticoids may be necessary. It is less common than   Disease not responding to prednisolone, especially if asso-
            LPE. Some cats have eosinophilic enteritis as part of a hyper-  ciated with hypoalbuminemia, sometimes requires immuno-
            eosinophilic syndrome (HES). The cause of feline HES is   suppressives (e.g., cyclosporine, chlorambucil, azathioprine).
            unknown, but immune-mediated and neoplastic mecha-   Cyclosporine seems to be reasonably effective and works
            nisms may be responsible. Less severely affected cats without   faster than azathioprine. However, relatively few dogs with
            HES seem to have a condition similar to canine EGE.  non–protein-losing chronic enteropathies require these
                                                                 immunosuppressive drugs. Failure of a dog to respond to
            Diagnosis                                            the various therapeutic trials followed by aggressive antiin-
            If IBD is defined as idiopathic inflammation, it is a diagnosis   flammatory  or  immunosuppressive  therapy  usually  means
            of exclusion and not just a histologic diagnosis. No physical   that  the  diagnosis  is incorrect.  Typically such  patients are
            examination, history, clinical pathology, imaging, or histo-  ultimately found to be dietary-responsive or antibiotic-
            logic findings are diagnostic of IBD. Diagnosis requires   responsive animals.
            elimination of known causes of diarrhea (e.g., dietary-  Feline LPE is approached a bit differently. First, some
            responsive, antibiotic-responsive, parasitic, neoplastic,   cats with chronic diarrhea will have complete resolution
            fungal, etc.) plus histology showing mucosal inflammatory   of clinical signs after parenteral cobalamin supplementa-
            infiltrates, architectural  changes (e.g., villus atrophy,  crypt   tion. Dietary-responsive diarrhea is common, but finding
            changes), and/or epithelial changes. Mucosal cytologic eval-  an elimination diet that the cat will eat can be challeng-
            uation is unreliable for diagnosing lymphocytic inflamma-  ing; hence, the clinician may have to settle for a mediocre
            tion because lymphocytes and plasma cells are normally   elimination diet that the patient will eat as opposed to a
            present in intestinal mucosa. Unfortunately, histologic diag-  more strict elimination diet that the patient refuses. Anti-
            nosis of mucosal inflammation is subjective, and biopsy   microbials (e.g., tylosin or metronidazole) are often helpful,
            samples are frequently overinterpreted with substantial   but administering the drug can be difficult or impossible
            inconsistency among pathologists. It can be extremely diffi-  for some clients. Because some cats make it extremely dif-
            cult to histologically distinguish well-differentiated small cell   ficult to perform good dietary and/or antimicrobial trials,
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