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Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy

BACKGROUND: Little is known about the spectrum of underlying disorders in dogs with unilateral masticatory muscle (MM) atrophy. OBJECTIVES: To evaluate the clinical presentation, magnetic resonance imaging (MRI) findings, and outcome of dogs with unilateral MM atrophy. ANIMALS: Sixty‐three client‐ow...

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Autores principales: Milodowski, Emily Jayne, Amengual‐Batle, Pablo, Beltran, Elsa, Gutierrez‐Quintana, Rodrigo, De Decker, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430959/
https://www.ncbi.nlm.nih.gov/pubmed/30556930
http://dx.doi.org/10.1111/jvim.15373
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author Milodowski, Emily Jayne
Amengual‐Batle, Pablo
Beltran, Elsa
Gutierrez‐Quintana, Rodrigo
De Decker, Steven
author_facet Milodowski, Emily Jayne
Amengual‐Batle, Pablo
Beltran, Elsa
Gutierrez‐Quintana, Rodrigo
De Decker, Steven
author_sort Milodowski, Emily Jayne
collection PubMed
description BACKGROUND: Little is known about the spectrum of underlying disorders in dogs with unilateral masticatory muscle (MM) atrophy. OBJECTIVES: To evaluate the clinical presentation, magnetic resonance imaging (MRI) findings, and outcome of dogs with unilateral MM atrophy. ANIMALS: Sixty‐three client‐owned dogs. METHODS: The medical database was retrospectively reviewed for dogs that underwent MRI for evaluation of unilateral MM atrophy. Imaging studies were reviewed and follow‐up information was obtained from telephone interviews. RESULTS: Presumptive trigeminal nerve sheath tumor (pTNST) was diagnosed in 30 dogs (47.6%); survival time varied from 1 day to 21 months (median, 5 months). Other extra‐axial mass lesions were observed in 13 dogs (20.6%); survival time varied from 6 days to 25 months (median, 2.5 months). In 18 dogs (28.6%), no abnormalities were observed on MRI; neurological signs only progressed in 1 dog. Diagnosis had a significant influence on the type of neurological abnormalities, with additional neurological deficits observed in most dogs with pTNST and in all dogs with other extra‐axial mass lesions. Diagnosis had a significant effect on euthanasia at the time of diagnosis and likelihood of neurological deterioration. Dogs with mass lesions were more likely to be euthanized or experience neurological deterioration, whereas these outcomes occurred less often in dogs in which no causative lesion could be identified. CONCLUSIONS AND CLINICAL IMPORTANCE: Trigeminal nerve sheath tumors should not be considered the only cause of unilateral MM atrophy. Our results illustrate the importance of performing a neurological examination and MRI when evaluating dogs with unilateral MM atrophy.
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spelling pubmed-64309592019-04-04 Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy Milodowski, Emily Jayne Amengual‐Batle, Pablo Beltran, Elsa Gutierrez‐Quintana, Rodrigo De Decker, Steven J Vet Intern Med SMALL ANIMAL BACKGROUND: Little is known about the spectrum of underlying disorders in dogs with unilateral masticatory muscle (MM) atrophy. OBJECTIVES: To evaluate the clinical presentation, magnetic resonance imaging (MRI) findings, and outcome of dogs with unilateral MM atrophy. ANIMALS: Sixty‐three client‐owned dogs. METHODS: The medical database was retrospectively reviewed for dogs that underwent MRI for evaluation of unilateral MM atrophy. Imaging studies were reviewed and follow‐up information was obtained from telephone interviews. RESULTS: Presumptive trigeminal nerve sheath tumor (pTNST) was diagnosed in 30 dogs (47.6%); survival time varied from 1 day to 21 months (median, 5 months). Other extra‐axial mass lesions were observed in 13 dogs (20.6%); survival time varied from 6 days to 25 months (median, 2.5 months). In 18 dogs (28.6%), no abnormalities were observed on MRI; neurological signs only progressed in 1 dog. Diagnosis had a significant influence on the type of neurological abnormalities, with additional neurological deficits observed in most dogs with pTNST and in all dogs with other extra‐axial mass lesions. Diagnosis had a significant effect on euthanasia at the time of diagnosis and likelihood of neurological deterioration. Dogs with mass lesions were more likely to be euthanized or experience neurological deterioration, whereas these outcomes occurred less often in dogs in which no causative lesion could be identified. CONCLUSIONS AND CLINICAL IMPORTANCE: Trigeminal nerve sheath tumors should not be considered the only cause of unilateral MM atrophy. Our results illustrate the importance of performing a neurological examination and MRI when evaluating dogs with unilateral MM atrophy. John Wiley & Sons, Inc. 2018-12-17 2019 /pmc/articles/PMC6430959/ /pubmed/30556930 http://dx.doi.org/10.1111/jvim.15373 Text en © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
Milodowski, Emily Jayne
Amengual‐Batle, Pablo
Beltran, Elsa
Gutierrez‐Quintana, Rodrigo
De Decker, Steven
Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title_full Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title_fullStr Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title_full_unstemmed Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title_short Clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
title_sort clinical findings and outcome of dogs with unilateral masticatory muscle atrophy
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430959/
https://www.ncbi.nlm.nih.gov/pubmed/30556930
http://dx.doi.org/10.1111/jvim.15373
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