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Feline dry eye syndrome of presumed neurogenic origin: a case report

CASE SUMMARY: A 14-year-old female spayed Abyssinian cat, which about 1 year previously underwent thoracic limb amputation, radiotherapy and chemotherapy for an incompletely excised vaccine-related fibrosarcoma, was presented for evaluation of corneal opacity in the left eye (OS). The ocular surface...

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Autores principales: Sebbag, Lionel, Pesavento, Patricia A, Carrasco, Sebastian E, Reilly, Christopher M, Maggs, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753927/
https://www.ncbi.nlm.nih.gov/pubmed/29318025
http://dx.doi.org/10.1177/2055116917746786
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author Sebbag, Lionel
Pesavento, Patricia A
Carrasco, Sebastian E
Reilly, Christopher M
Maggs, David J
author_facet Sebbag, Lionel
Pesavento, Patricia A
Carrasco, Sebastian E
Reilly, Christopher M
Maggs, David J
author_sort Sebbag, Lionel
collection PubMed
description CASE SUMMARY: A 14-year-old female spayed Abyssinian cat, which about 1 year previously underwent thoracic limb amputation, radiotherapy and chemotherapy for an incompletely excised vaccine-related fibrosarcoma, was presented for evaluation of corneal opacity in the left eye (OS). The ocular surface of both eyes (OU) had a lackluster appearance and there was a stromal corneal ulcer OS. Results of corneal aesthesiometry, Schirmer tear test-1 (STT-1) and tear film breakup time revealed corneal hypoesthesia, and quantitative and qualitative tear film deficiency OU. Noxious olfactory stimulation caused increased lacrimation relative to standard STT-1 values suggesting an intact nasolacrimal reflex. Various lacrimostimulants were administered in succession; namely, 1% pilocarpine administered topically (15 days) or orally (19 days), and topically applied 0.03% tacrolimus (47 days). Pilocarpine, especially when given orally, was associated with notable increases in STT-1 values, but corneal ulceration remained/recurred regardless of administration route, and oral pilocarpine resulted in gastrointestinal upset. Tacrolimus was not effective. After 93 days, the cat became weak and lame and a low thyroxine concentration was detected in serum. The cat was euthanized and a necropsy performed. Both lacrimal glands were histologically normal, but chronic neutrophilic keratitis and reduced conjunctival goblet cell density were noted OU. RELEVANCE AND NOVEL INFORMATION: The final diagnosis was dry eye syndrome (DES) of presumed neurogenic origin, associated with corneal hypoesthesia. This report reinforces the importance of conducting tearfilm testing in cats with ocular surface disease, as clinical signs of DES were different from those described in dogs.
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spelling pubmed-57539272018-01-09 Feline dry eye syndrome of presumed neurogenic origin: a case report Sebbag, Lionel Pesavento, Patricia A Carrasco, Sebastian E Reilly, Christopher M Maggs, David J JFMS Open Rep Case Report CASE SUMMARY: A 14-year-old female spayed Abyssinian cat, which about 1 year previously underwent thoracic limb amputation, radiotherapy and chemotherapy for an incompletely excised vaccine-related fibrosarcoma, was presented for evaluation of corneal opacity in the left eye (OS). The ocular surface of both eyes (OU) had a lackluster appearance and there was a stromal corneal ulcer OS. Results of corneal aesthesiometry, Schirmer tear test-1 (STT-1) and tear film breakup time revealed corneal hypoesthesia, and quantitative and qualitative tear film deficiency OU. Noxious olfactory stimulation caused increased lacrimation relative to standard STT-1 values suggesting an intact nasolacrimal reflex. Various lacrimostimulants were administered in succession; namely, 1% pilocarpine administered topically (15 days) or orally (19 days), and topically applied 0.03% tacrolimus (47 days). Pilocarpine, especially when given orally, was associated with notable increases in STT-1 values, but corneal ulceration remained/recurred regardless of administration route, and oral pilocarpine resulted in gastrointestinal upset. Tacrolimus was not effective. After 93 days, the cat became weak and lame and a low thyroxine concentration was detected in serum. The cat was euthanized and a necropsy performed. Both lacrimal glands were histologically normal, but chronic neutrophilic keratitis and reduced conjunctival goblet cell density were noted OU. RELEVANCE AND NOVEL INFORMATION: The final diagnosis was dry eye syndrome (DES) of presumed neurogenic origin, associated with corneal hypoesthesia. This report reinforces the importance of conducting tearfilm testing in cats with ocular surface disease, as clinical signs of DES were different from those described in dogs. SAGE Publications 2018-01-02 /pmc/articles/PMC5753927/ /pubmed/29318025 http://dx.doi.org/10.1177/2055116917746786 Text en © The Author(s) 2017 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Sebbag, Lionel
Pesavento, Patricia A
Carrasco, Sebastian E
Reilly, Christopher M
Maggs, David J
Feline dry eye syndrome of presumed neurogenic origin: a case report
title Feline dry eye syndrome of presumed neurogenic origin: a case report
title_full Feline dry eye syndrome of presumed neurogenic origin: a case report
title_fullStr Feline dry eye syndrome of presumed neurogenic origin: a case report
title_full_unstemmed Feline dry eye syndrome of presumed neurogenic origin: a case report
title_short Feline dry eye syndrome of presumed neurogenic origin: a case report
title_sort feline dry eye syndrome of presumed neurogenic origin: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753927/
https://www.ncbi.nlm.nih.gov/pubmed/29318025
http://dx.doi.org/10.1177/2055116917746786
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