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1.
Vet Res Commun ; 47(4): 1845-1859, 2023 Dec.
Article de Anglais | MEDLINE | ID: mdl-37133704

RÉSUMÉ

The aim of this study was to evaluate routinely used tests to diagnose cats in early stages of chronic kidney disease (CKD) and to describe a model for evaluating these variables simultaneously. Apparently healthy cats were screened using serum creatinine (sCr), point-of-care symmetric dimethylarginine (POC SDMA), urinalysis, urine protein/creatinine ratio (UPC) and imaging evaluation. Those parameters were compared to glomerular filtration rate (GFR) assessed by renal scintigraphy. Forty-four cats were included and consisted of 14 (31.8%) healthy cats (absence of abnormalities in renal morphology and sCr less than 1.6 mg/dL), 20 (45.5%) cats classified as CKD I (presence of abnormalities in renal morphology and sCr less than 1.6 mg/dL) and ten (22.7%) as CKD II (sCr equal to or greater than 1.6 mg/dL, with or without abnormalities in renal morphology). A large number (40.9%) of apparently healthy cats presented reduction in GFR, which included half of CKD I patients. Point-of-care SDMA was not a good predictor for decreased GFR, nor was it correlated with the variables GFR and sCr. Glomerular filtration rate was significantly lower in CKD I and II groups in comparison with healthy cats, but there was no significant difference between the CKD I and II groups. Multivariate logistic regression model identified three variables that affected the odds of a cat having decreased GFR (< 2.5 mL/min/kg): sCr (OR = 18.3; p = 0.019; CI = 1.6-207.2), and the ultrasonographic findings 'reduced corticomedullary definition' (OR = 19.9; p = 0.022; CI = 1.6-254.0) and 'irregular contour' (OR = 65.6; p = 0.003; CI = 4.2-1038.2). Renal ultrasonography evaluation should always be considered for screening early CKD in apparently healthy cats.


Sujet(s)
Maladies des chats , Insuffisance rénale chronique , Chats , Animaux , Débit de filtration glomérulaire/médecine vétérinaire , Créatinine , Systèmes automatisés lit malade , Marqueurs biologiques , Rein/imagerie diagnostique , Arginine , Insuffisance rénale chronique/imagerie diagnostique , Insuffisance rénale chronique/médecine vétérinaire , Scintigraphie , Maladies des chats/imagerie diagnostique
2.
Ci. Rural ; 47(5)2017.
Article de Anglais | VETINDEX | ID: vti-710088

RÉSUMÉ

ABSTRACT: Neuroblastic tumors can originate from the central neuraxis, olfactory epithelium, adrenal medullary region or autonomous system. Ganglioneuroblastoma are a type of neuroblastic tumor, with very few case descriptions in animals. Diagnosis of facial nerve ganglioneuroblastoma was made in a feline leukemia virus-positive 11-month-old cat. The cat had hyporexia, left head tilt, depressed mental state, horizontal nystagmus, inability to retract the pinched left lip, anisocoria, ptosis, and absence of the menace reflex. Gross necropsy showed a mass at the left facial nerve root region. Histological examination of this mass showed neoplastic proliferation of neuroblasts arranged in a cohesive pattern and mature ganglion cells. Ganglion cells were positive for neurofilament, neuron-specific enolase, S100, and glial fibrillary acidic protein by immunohistochemistry, while neuroblasts were positive for vimentin, S100, neuron-specific enolase and feline leukemia virus.


RESUMO: Tumores neuroblásticos podem se originar do neuraxis central, do epitélio olfativo, região medular da adrenal ou do sistema autônomo. O ganglioneuroblastoma é um tipo desses tumores, com raras descrições em animais. O diagnóstico de ganglioneuroblastoma de nervo facial foi feito em um gato de 11 meses de idade, sorologicamente positivo para o vírus da leucemia felina. O gato tinha hiporexia, inclinação de cabeça para o lado esquerdo, estado mental deprimido, nistagmo horizontal, incapacidade em retrair o lábio esquerdo quando pinçado, anisocoria, ptose e ausência do reflexo de ameaça. Na necropsia visualizou-se uma massa na região da raiz do nervo facial esquerdo. O exame histológico mostrou proliferação neoplásica de neuroblastos arranjados de maneira coesa, e células ganglionares maduras. As células ganglionares foram imunorreativas na imuno-histoquímica para neurofilamento, enolase neurônio específica, S-100 e proteína ácida glial fibrilar. Enquanto os neuroblastos foram positivos para vimentina, S-100, enolase neurônio específica e vírus da leucemia felina.

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