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1102  Section 10  Renal and Genitourinary Disease

            Table 121.1  Select breeds of dogs with familial glomerulopathies  ascites, or both, are sometimes noted and consistent
  VetBooks.ir  Breed           Glomerular disease(s)          with nephrotic syndrome. Occasionally, there is physical
                                                              evidence of thromboembolic disease, such as dyspnea or

             Beagle            Amyloidosis, primary glomerulopathy  a decreased or absent peripheral pulse. Evidence of a
                                                              predisposing inflammatory, infectious, or neoplastic
             Bernese mountain dog  Mesangiocapillary glomerulonephritis  process may be detected during the physical examina-
             Bull mastiff      Glomerulosclerosis             tion. The kidneys of affected animals are variable in size.
             Bull terrier      Hereditary nephritis           Animals with chronic kidney disease often have small,
             Dalmatian         Hereditary nephritis           firm, irregularly shaped kidneys, whereas those with less
                                                              severe or long‐standing disease often have normal‐sized
             Doberman pinscher  Glomerulosclerosis, cystic glomerular   or, occasionally, enlarged kidneys.
                               atrophy
             English cocker spaniel  Hereditary nephritis
             English foxhound  Amyloidosis                      Diagnosis
             Greyhound         Glomerular vasculopathy and necrosis
             Newfoundland      Glomerulosclerosis             When proteinuria is detected, there are three key ele-
             Pembroke Welsh corgi  Glomerulosclerosis, cystic glomerular   ments that need to be assessed: localization, persistence,
                               atrophy                        and magnitude. Although proteinuria is the hallmark
             Rottweiler        Atrophic glomerulopathy        of  glomerular disease, it can also occur secondary to
             Samoyed           Hereditary nephritis           prerenal, postrenal or renal tubular causes. The magni-
                                                              tude of proteinuria is generally assessed via the urine
             Shar‐pei          Amyloidosis                    protein:creatinine ratio (UPC). Persistent renal pro-
             Soft‐coated wheaten   Podocytopathy              teinuria that is of high magnitude (i.e., UPC >2) is most
             terrier                                          likely of glomerular origin; however, there is no range of
                                                              numbers that is diagnostic for any one renal disease and
                                                              the overlap in expected ranges is too broad to be clini-
              History and Clinical Signs                      cally reliable. In fact, glomerular lesions have been seen
                                                              in dogs without proteinuria. Urine albumin can also
            Dogs and cats with glomerular disease can present with   be  used to assess proteinuria. Microalbuminuria may
            a variety of clinical signs, determined by the severity of   develop before the UPC is increased. It therefore seems
            proteinuria or renal disease and the presence or absence   reasonable to conclude that a dog or cat with persistent
            of any systemic disorders. They may be asymptomatic,   microalbuminuria of increasing magnitude should be
            have nonspecific signs (e.g., anorexia, weight loss, lethargy)   assessed as having an injurious process to the glomerular
            or have signs of more advanced renal disease (e.g., polyu-  filtration barrier and may eventually develop overt
            ria, polydipsia, vomiting, diarrhea, halitosis). Animals   proteinuria.
            with severe urinary protein loss may develop nephrotic   Once glomerular disease is suspected, a comprehen-
            syndrome and have evidence of fluid retention (e.g.,   sive diagnostic evaluation is recommended for all dogs
            abdominal enlargement consistent with ascites, periph-  and cats which includes urinalysis, serial UPC measure-
            eral edema). Animals also may develop clinical signs   ments, completed blood count, biochemical profile, and
            from thromboembolism (e.g., dyspnea, loss of limb func-  blood pressure measurement. Urine culture is warranted
            tion), or hypertension (e.g., acute blindness, or recent   if there is pyuria, hematuria, bacteriuria, dilute urine
            onset of neurologic signs or cardiac murmur). When glo-  (e.g., urine specific gravity <1.025) or concurrent dis-
            merular disease is suspected, the history should include   eases which might predispose the patient to urinary tract
            questions about the environment, possible exposure to   infection (e.g., hyperadrenocorticism). Animals with
            infectious diseases as well as relevant drug or dietary   potential exposure to infectious diseases should undergo
            exposure.                                         the  appropriate  testing.  Any  concominant  extrarenal
             Complete physical examinations should be performed   disease should be evaluated further (e.g., aspriation
            on dogs and cats with suspected glomerular disease,   cytology of cutaneous masses, appropriate testing for
            including body condition score, retinal and rectal exami-  hyperadrenocorticism). If proteinuria is of high magni-
            nations. Physical examination is often unremarkable.   tude (i.e., UPC >3.5), associated with hypoalbuminemia,
            Poor body condition or poor hair coat may be nonspe-  azotemia, or hypertension, or progressive or nonre-
            cific evidence of systemic disease. Animals with advanced   sponsive to treatment, additional diagnostics including
            renal  disease  may  have  oral  ulcerations, pale  mucous   but not limited to abdominal ultrasound, thoracic
            membranes, or dehydration. Subcutaneous edema or     radiographs, more extensive evaluation for infectious
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