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Acquired nephrogenic diabetes insipidus in a dog with leptospirosis

A 5 year old male neutered Cairn Terrier was evaluated for signs of polyuria and polydipsia. Initial hematology and chemistry panels were unremarkable and urinalysis showed a persistent hyposthenuria. Eleven days later, the dog became lethargic, inappetent and had developed acute renal failure. The...

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Autores principales: Etish, Jamie L, Chapman, Peter S, Klag, Alan R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005616/
https://www.ncbi.nlm.nih.gov/pubmed/24739820
http://dx.doi.org/10.1186/2046-0481-67-7
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author Etish, Jamie L
Chapman, Peter S
Klag, Alan R
author_facet Etish, Jamie L
Chapman, Peter S
Klag, Alan R
author_sort Etish, Jamie L
collection PubMed
description A 5 year old male neutered Cairn Terrier was evaluated for signs of polyuria and polydipsia. Initial hematology and chemistry panels were unremarkable and urinalysis showed a persistent hyposthenuria. Eleven days later, the dog became lethargic, inappetent and had developed acute renal failure. The dog was ultimately euthanized due to a poor response to treatment. Microscopic agglutination titres were consistent with a diagnosis of leptospirosis. The initial hyposthenuria in this case was consistent with acquired nephrogenic diabetes insipidus. This is an uncommon presentation of leptospirosis that has not previously been described to progress to acute renal failure. Leptospirosis should be considered as a differential diagnosis in any dog presenting with polyuria and polydipsia and these patients should be treated as a zoonotic risk.
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spelling pubmed-40056162014-05-01 Acquired nephrogenic diabetes insipidus in a dog with leptospirosis Etish, Jamie L Chapman, Peter S Klag, Alan R Ir Vet J Case Report A 5 year old male neutered Cairn Terrier was evaluated for signs of polyuria and polydipsia. Initial hematology and chemistry panels were unremarkable and urinalysis showed a persistent hyposthenuria. Eleven days later, the dog became lethargic, inappetent and had developed acute renal failure. The dog was ultimately euthanized due to a poor response to treatment. Microscopic agglutination titres were consistent with a diagnosis of leptospirosis. The initial hyposthenuria in this case was consistent with acquired nephrogenic diabetes insipidus. This is an uncommon presentation of leptospirosis that has not previously been described to progress to acute renal failure. Leptospirosis should be considered as a differential diagnosis in any dog presenting with polyuria and polydipsia and these patients should be treated as a zoonotic risk. BioMed Central 2014-04-17 /pmc/articles/PMC4005616/ /pubmed/24739820 http://dx.doi.org/10.1186/2046-0481-67-7 Text en Copyright © 2014 Etish et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Etish, Jamie L
Chapman, Peter S
Klag, Alan R
Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title_full Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title_fullStr Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title_full_unstemmed Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title_short Acquired nephrogenic diabetes insipidus in a dog with leptospirosis
title_sort acquired nephrogenic diabetes insipidus in a dog with leptospirosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005616/
https://www.ncbi.nlm.nih.gov/pubmed/24739820
http://dx.doi.org/10.1186/2046-0481-67-7
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