Peer-reviewed veterinary case report
Eye changes in dogs with distemper virus dry eye disease
By de Almeida, Denize E et al.·Published in Veterinary ophthalmology·2009·Department of Internal Medicine, United States·View original on PubMed →
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Original publication title: Conjunctival effects of canine distemper virus-induced keratoconjunctivitis sicca.
- Species:
- dog
Plain-English summary
A group of dogs with eye problems was studied to understand the effects of canine distemper virus (CDV) on a condition called keratoconjunctivitis sicca (KCS), which causes dry eyes. The dogs showed symptoms like low tear production, red eyes, and discharge. Both CDV-induced and non-infectious KCS had similar changes in the eye tissues, indicating that they may have similar causes related to inflammation and lack of tears. The study suggests that treatment for both types of KCS could be similar, focusing on managing inflammation and improving tear production.
People also search for: dog eye discharge treatment · canine distemper virus symptoms · dry eyes in dogs treatment
Abstract
OBJECTIVE: This study compared the histopathology of canine distemper virus (CDV)-induced keratoconjunctivitis sicca (KCS) to non-infectious KCS in conjunctival tissues. ANIMALS STUDIED: Forty mongrel dogs were assigned to three distinct groups: (i) non-infectious KCS (G1, n = 10), (ii) CDV-induced KCS (G2, n = 20), and (iii) healthy animals without any ocular alterations (G3, n = 10). PROCEDURE: IgG titers and physical and ophthalmic examinations (e.g. Schirmer tear test [STT], tonometry, biomicroscopy, indirect biomicroscopy, and fluorescein test) were performed on all dogs. Conjunctival biopsies were collected and examined microscopically. RESULTS: Non-infectious and CDV-induced KCS demonstrated similar histopathological changes. Both types of KCS correlated with low STT, conjunctival hyperemia, mucopurulent ocular discharge, predominant lymphoplasmacytic infiltration, and acantholysis and keratinization of the ocular surface. G1 had lower conjunctival goblet cell counts than G3. Inclusion bodies were sporadically found in conjunctival samples of dogs from G2. The severity of ocular lesions in G1 and G2 did not correlate with the histopathological findings. CONCLUSIONS: Dogs with non-infectious and CDV-induced KCS had very similar conjunctival histopathology. Our findings suggest that the pathophysiology of CDV-induced KCS is likely to be the same as non-infectious KCS, that is, a result of lacrimal deficiency and inflammation of the ocular surface.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19604335/