ABSTRACT
A histological and immunohistological study of the kidneys of 115 dogs, with and without clinical signs of spontaneous renal disease, was performed to prove the applicability of the WHO criteria for the classification of human glomerulopathy. Aside from the morphological investigation of paraffin and resin semithin sections, deposits of immunoglobulins, the complement component C3, and fibrinogen were observed immunoenzymatically in paraffin-embedded tissue specimens. From this, eight different types of glomerular lesions with various frequencies were identified: minor glomerular abnormalities (28 cases), focal and segmental hyalinosis and sclerosis (12 cases), focal glomerulonephritis (GN; 18 cases), diffuse membranous GN (nine cases), diffuse mesangial proliferative GN (2 cases), diffuse endocapillary proliferative GN (five cases), diffuse mesangiocapillary GN (25 cases), diffuse sclerosing GN (11 cases) und unclassified GN (two cases). In one case, renal dysplasia was diagnosed and two dogs did not present glomerular alterations. The results are discussed with regard to human glomerular diseases and pathogenic mechanisms.
Subject(s)
Dog Diseases/classification , Glomerulonephritis/veterinary , Kidney Diseases/veterinary , Kidney Glomerulus/pathology , Animals , Complement C3/analysis , Dog Diseases/pathology , Dogs , Female , Fibrinogen/analysis , Glomerulonephritis/classification , Glomerulonephritis/pathology , Immunoglobulins/analysis , Immunohistochemistry/methods , Kidney Diseases/classification , Kidney Diseases/pathology , Kidney Glomerulus/chemistry , MaleABSTRACT
In the dog, massive proteinuria and/or the nephrotic syndrome have been commonly associated with renal amyloidosis and membranous glomerulonephritis. Primary glomerulopathies associated with the nephrotic syndrome in man also include minimal change nephrotic syndrome and focal glomerular sclerosis. A 4-year-old Collie dog is described with clinical, histological, immunohistological, and ultrastructural findings similar to those which characterize the minimal change nephrotic syndrome (MCNS) in man.