Corneal diseases represent a significant proportion of feline ophthalmic conditions encountered in clinical practice. The feline cornea has unique characteristics that predispose cats to specific pathologies not commonly seen in other species.
Overview and Clinical Importance
Corneal diseases represent a significant proportion of feline ophthalmic conditions encountered in clinical practice. The feline cornea has unique characteristics that predispose cats to specific pathologies not commonly seen in other species. Understanding these conditions is essential for the NAVLE, as corneal diseases directly affect vision, comfort, and quality of life in affected patients.
Unlike dogs, cats have primary conjunctival and corneal pathogens, particularly feline herpesvirus-1 (FHV-1), which causes approximately 80-90% of infectious keratitis cases. This virus is ubiquitous in the cat population, with an estimated 80-95% of cats being latently infected. Understanding the relationship between FHV-1 and corneal disease is fundamental to feline ophthalmology.
| Layer |
Structure |
Clinical Significance |
| Epithelium |
5-7 cell layers; lipophilic; complete turnover in 7 days; heals within 48-72 hours |
Barrier to hydrophilic fluorescein; FHV-1 primarily infects this layer |
| Stroma |
90% of corneal thickness; collagen fibrils and keratocytes; hydrophilic |
Takes up fluorescein; heals slowly with scarring; sequestrum forms here |
| Descemet's Membrane |
Basement membrane of endothelium; elastic; thickens with age |
Lipophilic - does NOT take up fluorescein; descemetocele appears clear |
| Endothelium |
Single cell layer; minimal regenerative capacity; contains Na+/K+-ATPase pumps |
Maintains corneal dehydration; damage causes edema; bullous keratopathy |
Feline Corneal Anatomy
The feline cornea is an avascular, transparent structure composed of four main layers: epithelium, stroma, Descemet's membrane, and endothelium. Understanding corneal layer anatomy is critical for assessing ulcer depth and determining appropriate treatment.
Corneal Layer Characteristics
High-YieldA descemetocele is a deep corneal ulcer that extends to Descemet's membrane. On fluorescein staining, the walls of the ulcer stain green (exposed stroma), but the floor remains clear because Descemet's membrane is lipophilic and does NOT take up fluorescein. This is a surgical emergency as perforation is imminent.
| Clinical Feature |
Description |
| Dendritic Ulcers |
PATHOGNOMONIC for FHV-1; linear, branching, tree-like pattern; best visualized with Rose Bengal stain |
| Geographic Ulcers |
Larger, map-like, irregular erosions; result from coalescence of dendritic ulcers; loose epithelial edges |
| Stromal Keratitis |
Non-ulcerative; immune-mediated; corneal opacity, neovascularization, pigmentation, scarring |
| Symblepharon |
Adhesion of conjunctiva to cornea or itself; common sequela in kittens; can cause blindness |
| Conjunctivitis |
Hyperemia, chemosis, serous to mucopurulent discharge; often bilateral in primary infection |
Feline Herpesvirus-1 Keratitis
Pathophysiology
Feline herpesvirus-1 (FHV-1) is an alphaherpesvirus with worldwide distribution. Following primary infection (usually in kittens 2-6 weeks old), the virus establishes lifelong latency in the trigeminal ganglion. Approximately 80% of infected cats become latent carriers, and 40-50% experience recrudescent disease triggered by stress, immunosuppression, or corticosteroid administration.
FHV-1 keratitis can manifest as: ulcerative keratitis (direct viral cytopathic effect) or stromal keratitis (immune-mediated response to viral antigen). Clinical signs develop 2-6 days after infection, with corneal epithelial damage from viral replication causing cell lysis.
Clinical Signs and Diagnosis
NAVLE Tip"DENDRITIC = DEFINITIVE" - If you see a dendritic (branching) corneal ulcer on the NAVLE, the diagnosis is FHV-1 keratitis. No other confirmatory testing is required because dendritic ulcers are PATHOGNOMONIC for herpesvirus infection in cats.
Treatment of FHV-1 Keratitis
High-YieldNEVER use acyclovir or valacyclovir in cats - they cause severe bone marrow suppression, hepatotoxicity, and nephrotoxicity that can be fatal. Famciclovir is the ONLY safe systemic antiviral for cats.
| Antiviral |
Route/Form |
Dosing |
Notes |
| Famciclovir |
Oral (systemic) |
40-90 mg/kg PO q8-12h |
Preferred systemic; converted to penciclovir; SAFE in cats |
| Cidofovir 0.5% |
Topical (compounded) |
1 drop q12h |
Long half-life; convenient dosing; expensive |
| Idoxuridine 0.1% |
Topical (compounded) |
1 drop q4-6h |
Well-tolerated; cost-effective; frequent dosing required |
| Trifluridine 1% |
Topical (Viroptic) |
1 drop q4-6h |
Most potent in vitro; often causes ocular irritation in cats |
Feline Corneal Sequestrum
Pathophysiology and Etiology
Corneal sequestrum (corneal mummification, corneal nigrum) is a condition UNIQUE to cats characterized by focal necrosis and brown-black pigmentation of the corneal stroma. The sequestrum represents devitalized corneal tissue that is gradually rejected by surrounding healthy cornea, acting as a foreign body and inducing inflammation.
Predisposing Factors
NAVLE TipGrid keratotomy is CONTRAINDICATED in cats! Unlike dogs with spontaneous chronic corneal epithelial defects (SCCEDs), cats do not develop true indolent ulcers. Performing grid keratotomy on a feline "non-healing" ulcer often induces sequestrum formation. If you see a question about treating a non-healing corneal ulcer in a cat, grid keratotomy is WRONG.
Clinical Signs and Diagnosis
The clinical appearance is pathognomonic: a focal, tan to dark brown-black plaque in the central or paracentral cornea. The lesion color ranges from translucent amber (early) to opaque black (advanced). Surrounding corneal vascularization and loose epithelial edges are common. The condition is typically extremely painful due to chronic epithelial erosion.
Diagnostic approach: Visual examination is typically sufficient for diagnosis. Fluorescein uptake may occur at the lesion periphery where epithelium is eroded. Schirmer tear test and tear break-up time should be performed to assess tear film. Corneal cytology can rule out concurrent bacterial infection.
Treatment Options
Exam Focus - Sequestrum Memory Aid: "PERSIAN PROBLEMS"
P = Persian/brachycephalic predisposition
E = Entropion/eyelid abnormalities
R = Recurring ulceration
S = Stromal necrosis with pigmentation
I = Irritation from chronic exposure
A = Antiviral therapy for FHV-1 component
N = No grid keratotomy in cats!
| Factor |
Mechanism/Notes |
| Brachycephalic Breeds |
Persian (71.5%), Himalayan, Exotic Shorthair, Burmese; exophthalmos, lagophthalmos, central corneal exposure |
| FHV-1 Infection |
55% of sequestra are FHV-1 positive; chronic ulceration predisposes to sequestrum formation |
| Entropion/Trichiasis |
Chronic mechanical irritation from eyelid or hair contact; 37% concurrent with entropion in one study |
| Grid Keratotomy |
CONTRAINDICATED in cats; 31% develop sequestrum after grid keratotomy for non-healing ulcers |
| Tear Film Abnormalities |
Qualitative or quantitative tear deficiency; corneal desiccation |
Feline Eosinophilic Keratitis
Pathophysiology
Eosinophilic keratitis (EK) is a chronic, progressive, inflammatory corneal disease characterized by infiltration of eosinophils into the corneal stroma. The exact etiology is unknown, but it is believed to be an immune-mediated hypersensitivity reaction. Up to 75% of affected cats test positive for FHV-1, suggesting a possible link, though the causal mechanism remains unclear.
Clinical Signs and Diagnosis
The clinical appearance is nearly pathognomonic: raised, white to pinkish plaques with corneal vascularization, typically starting at the superotemporal limbus (76.8% of cases). A white, friable, gritty exudate often adheres to the surface. The condition is usually unilateral initially (75.6%), though bilateral involvement can occur.
Definitive diagnosis requires corneal cytology: Use a cytobrush, Kimura spatula, or blunt scalpel blade to collect samples from the plaque after topical anesthesia. The presence of even ONE eosinophil is considered diagnostic, as eosinophils are not normally present on healthy feline corneas.
Treatment
High-YieldEK requires LIFELONG or long-term treatment. Recurrence rates are 64% or higher when treatment is stopped. The goal is to achieve clinical remission and then find the lowest effective maintenance dose. If concurrent ulceration exists, treat the ulcer first before initiating corticosteroids.
| Treatment |
Indications |
Considerations |
| Medical Management |
Superficial lesions; comfortable patient; financial constraints; anesthetic risk |
Sloughing takes weeks to months; risk of deepening; lubricants, antibiotics, antivirals |
| Keratectomy |
GOLD STANDARD; all depths; painful patients; complete excision |
Requires operating microscope; incomplete resection leads to 25% recurrence |
| Conjunctival Graft |
Deep keratectomy (greater than 50% stromal depth); provides tectonic support |
Pedicle or island graft; brings blood supply for healing; reduces recurrence |
| Corneoconjunctival Transposition |
Central lesions requiring clear cornea for vision |
Slides peripheral cornea into central defect; superior visual outcomes |
Feline Corneal Ulceration
Ulcer Classification and Assessment
In feline patients, superficial corneal ulceration should be presumed to result from FHV-1 until proven otherwise. Other causes (trauma, eyelid abnormalities, tear film deficiencies) are less common in cats compared to dogs. Corneal ulcers are classified by depth, which determines treatment approach.
NAVLE TipWhen evaluating a corneal ulcer, always assess four key factors: (1) ETIOLOGY - The most important factor! If the underlying cause is not addressed, the ulcer will not heal. (2) DEPTH - Determines treatment urgency and approach. (3) COMPLICATING FACTORS - Infection or matrix metalloproteinase (MMP) activity causing "melting." (4) PROGRESSION - Is it deepening? How quickly?
| Medication |
Dosing |
Notes |
| Topical Corticosteroids |
Prednisolone 1% or Dexamethasone 0.1% q6-12h, taper |
First-line treatment; CONTRAINDICATED if ulcer present; may reactivate FHV-1 |
| Topical Cyclosporine 1.5% |
q12h |
88.6% response rate; safe with ulcers; may cause blepharitis |
| Topical Megestrol Acetate 0.5% |
q8-12h, taper |
Excellent results; safe even with concurrent ulcers; minimal systemic effects |
| Concurrent Antiviral |
Cidofovir q12h or Famciclovir PO |
Always consider with corticosteroid use due to FHV-1 association |
Feline Acute Bullous Keratopathy
Feline acute bullous keratopathy (acute corneal hydrops) is a unique feline condition characterized by sudden onset of focal or diffuse stromal edema with corneal protrusion. The edema is caused by acute Descemet's membrane rupture, allowing aqueous humor to flood the stroma.
Clinical features: Acute onset; marked corneal edema and bulging visible from lateral view; may be focal, geographic, or complete. Unlike endothelial disease, bullous keratopathy often resolves spontaneously with supportive care. There is a reported association with systemic cyclosporine administration. Left untreated, corneal rupture and loss of the eye can occur.
| Ulcer Type |
Characteristics |
Treatment Approach |
| Superficial |
Epithelial loss only; diffuse fluorescein uptake; most common in cats |
Antivirals, topical antibiotics, lubricants; should heal in 5-7 days |
| Stromal |
Loss of epithelium plus stroma; visible crater or divot |
Antivirals, antibiotics, atropine; monitor for deepening; consider referral |
| Descemetocele |
Full stromal loss; Descemet's membrane exposed; walls stain, floor clear |
SURGICAL EMERGENCY; conjunctival graft or corneal transplant needed |
| Perforated |
Full-thickness; aqueous leakage; iris may plug hole; shallow anterior chamber |
SURGICAL EMERGENCY; immediate referral; E-collar; systemic antibiotics |
Summary: Differential Diagnosis of Feline Corneal Diseases
| Disease |
Key Clinical Finding |
Breed Predisposition |
Primary Treatment |
| FHV-1 Keratitis |
Dendritic ulcers (PATHOGNOMONIC) |
Any breed |
Antivirals (famciclovir, cidofovir) |
| Corneal Sequestrum |
Brown-black corneal plaque |
Persian, Himalayan, Burmese, Siamese |
Keratectomy with grafting |
| Eosinophilic Keratitis |
White-pink plaques at dorsotemporal limbus |
Any breed; median age 5 years |
Topical corticosteroids or cyclosporine |
| Bullous Keratopathy |
Acute corneal edema and bulging |
Any breed |
Supportive; often self-resolving |