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Renal Crest Proliferative Lesions in Cats with Chronic Kidney Disease.
White, Joanna D; Bosward, Katrina L; Norris, Jacqueline M; Malik, Richard; Lindsay, Scott A; Canfield, Paul J.
Afiliación
  • White JD; Sydney School of Veterinary Science, University of Sydney, Sydney, New South Wales, Australia. Electronic address: jwhite@sashvets.com.
  • Bosward KL; Sydney School of Veterinary Science, University of Sydney, Sydney, New South Wales, Australia.
  • Norris JM; Sydney School of Veterinary Science, University of Sydney, Sydney, New South Wales, Australia.
  • Malik R; Centre for Veterinary Education, Veterinary Science Conference Centre B22, University of Sydney, Sydney, New South Wales, Australia.
  • Lindsay SA; School of Animal and Veterinary Sciences, Faculty of Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Canfield PJ; Sydney School of Veterinary Science, University of Sydney, Sydney, New South Wales, Australia.
J Comp Pathol ; 187: 52-62, 2021 Aug.
Article en En | MEDLINE | ID: mdl-34503654
ABSTRACT
In a histopathological study of the renal crest (RC) of kidneys of cats with chronic kidney disease (CKD), 58/90 (64%) had epithelial proliferation. Of these, 33 cats had hyperplasia of the collecting duct (CD) epithelium (CDH) alone, eight had hyperplasia of the urothelium covering the RC (RCUH), of which one had concurrent abaxial renal pelvic urothelial hyperplasia (UH), and eight had both CDH and RCUH. CDH or RCUH were present in five cats with marked dysplasia of the CD epithelium (CDD) and four cats with invasive carcinomas, which also had epithelial dysplasia. All nine cats with marked dysplasia or neoplasia of the RC also had substantially altered RC contours due to focal haemorrhage, papillary necrosis or fibrosis. Three of the carcinomas had a strong desmoplastic response. In control cats, both urothelial (RC and renal pelvis) and tubular (CD and distal tubular) cells were immunopositive for cytokeratin (CK; AE1/AE3), tubular epithelial cells were positive for vimentin (Vim) and aquaporin 2 (Aq2), while urothelial cells were positive for p63. PAX8 immunolabelling was difficult to validate. CD and UH labelling was similar to control tissue. While urothelial dysplasia had the same immunolabelling pattern as UH and control tissue, CDD was generally immunonegative for Aq2. As immunolabelling of the four carcinomas did not distinguish between tubular and urothelial origin, with three positive for both Vim and p63, all were broadly designated as RC carcinomas. Overall, proliferative epithelial lesions are common in cats with CKD and form a continuum from simple hyperplasia to neoplasia of the urothelium or CD of the RC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Enfermedades de los Gatos / Insuficiencia Renal Crónica / Neoplasias Renales Límite: Animals Idioma: En Revista: J Comp Pathol Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Enfermedades de los Gatos / Insuficiencia Renal Crónica / Neoplasias Renales Límite: Animals Idioma: En Revista: J Comp Pathol Año: 2021 Tipo del documento: Article
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