Pathological findings in dogs with renal dysplasia in Southern Brazil

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Abstract

Renal dysplasia results from a disturbance which occurs during nephrogenesis. The disease may be unilateral or bilateral, and leads to abnormal kidney differentiation leading to renal failure in young dogs. Several agents, including viruses, can cause the dysplasia till three months after birth, when the early nephron formation of the developing kidney is completed. Eleven renal dysplasia cases were diagnosed in 186 dogs with renal failure of 5,846 dogs necropsied in the Veterinary Pathology Sector, Federal University of Rio Grande do Sul, in the period 2002-2013. Tissue samples collected during necropsy were fixed in 10% formaldehyde and stained with hematoxylin-eosin (HE) and Masson's trichrome protocol. Upon necropsy, kidneys were pale, smaller than normal, irregular and firm, and presented lower cortex diameter. Some exhibited cysts and whitish, parallel radially arranged striae in the medulla. Primary and secondary renal lesions were observed during histological examination. Primary lesions included fetal glomeruli and tubules, quantitative reduction in glomeruli, adenomatous tubules, and persistence of metanephric ducts. As for secondary lesions, Masson trichrome staining revealed intense interstitial fibrosis in all cases; furthermore, dilation of tubules and of Bowman's capsules, glomerular atrophy, and glomerulosclerosis were observed. Even though most cases were associated with breed, the results obtained indicate high prevalence of renal dysplasia in mixed-breed dogs, possibly because they were the majority of animals referred for necropsy. Although primary lesions were easily identified using HE, Masson's trichrome protocol is useful to characterize the extent of fibrosis.

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Guimarães, L. L. B., Reis, M. de O., Hesse, K. L., Boabaid, F. M., Pavarini, S. P., Sonne, L., & Driemeier, D. (2014). Pathological findings in dogs with renal dysplasia in Southern Brazil. Pesquisa Veterinaria Brasileira, 34(12), 1227–1230. https://doi.org/10.1590/s0100-736x2014001200014

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