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. 2020 Aug 20;68(9):1764–1773. doi: 10.4103/ijo.IJO_928_20

Table 1.

Comparison of the clinical features between the common viral anterior uveitis aetiologies

Variables Herpes simplex virus (HSV) Varicella-zoster virus (VZV) Cytomegalovirus (CMV) Rubella virus (RV) Rubella associated FUS

Acute (Posner Schlossman like syndrome) Chronic

Chronic CMV anterior uveitis CMV-associated Fuchs uveitis syndrome (FUS)
Age 40-50 years >60 years Immuncompromised patients (any age) 30-50 years 40-70 years 40-70 years 20-40 years (Mean: 35±12 years)
Gender No predilection No predilection Males (65%) Males Males (80%) No predilection
Race All All Predominantly Asian population Western population Predominantly Asian population Western population
Laterality Mostly unilateral (bilateral in 18%) Unilateral Unilateral Mostlty unilateral (bilateral in 7%) Mostly unilateral (bilateral in 7%) Mostly unilateral (bilateral in 14%)
Course Acute, recurrent Acute, recurrent Acute, recurrent Chronic Chronic Chronic
Intraocular pressure Acute spikes (38-90%) Acute spikes (40-75%) Very high (up to 50 mmHg) during acute episodes (100%) Very high (43.5±9.8 mmHg); persistently elevated Very high (43.5±9.8 mmHg); persistently elevated (73.3%) Persistent elevation (25%)
Dermal manifestations h/o fever or blisters/grouped vesicles occurring at the border of the eyelids with diffuse edema Vesicular rash involving the ophthalmic division of the trigeminal nerve None None None None
Conjunctival injection Moderate to severe Moderate to severe Mild Mild Mild None
Corneal sensation May be reduced May be reduced (more profound and diffuse hypoaesthesia than HSV) Intact Intact Intact Intact
Epithelial keratitis Dendritic ulcers (usually branching, with well-developed terminal bulb) Pseudodendritic ulcers (less regular branching, few terminal dilatations) None None None None
Stromal keratitis Disciform keratitis; Interstitial keratitis; Immune ring keratitis Nummular keratitis; Limbal keratitis; Immune ring keratitis Immune ring keratitis None
Corneal scars Present (33%) Present (25%) Rare None
Endotheliitis May be present May be present May be present May be present Nodular endothelial lesions surrounded by a translucent halo and occasional pigmentation None
Keratic precipitates
Size Small to medium Small to medium Medium to large (39%) Small Fine and stellate (44%) Fine, may be stellate
Distribution Central, paracentral, diffuse, may be in Arlt’s triangle or in the same distribution as inflamed cornea Central, paracentral, diffuse, may be in Arlt’s triangle or in the same distribution as inflamed cornea Single or few, distributed centrally or in peripheral cornea; may have coin like lesions May have a coin like lesions Diffusely distributed; may have a coin like lesions (ring or linear pattern) Diffuse
Colour White, may be pigmented White, may be pigmented White or gray White or gray, may be brown White or gray, may have pigmentation White, never pigmented
Endothelial cell count Normal Normal Reduced Reduced Reduced Normal
Anterior chamber inflammation Moderate to severe Severe. Usually more than HSV Mild Mild Mild Mild
Iris
Iridoplegia May be present during acute phase causing pupil flattening or D shaped pupil May be present during acute phase causing pupil flattening or D shaped pupil Absent Absent Absent Absent
Iris atrophy Sectoral or patchy atrophy with transillumination defects, spiral iris atrophy Sectoral atrophy with transillumination defects, rarely massive iris atrophy with gross sphincter damage Mostly absent, rarely diffuse stromal iris atrophy Rarely sectoral, stromal iris atrophy, no transillumination defects Diffuse stromal iris atrophy, no transillumination defects Diffuse atrophy, fine iris transillumination defects
Posterior synechiae May be present May be present Absent Absent Absent Absent
Pupil shape May be irregular May be irregular Round Round Round Round
Elevated IOP Elevated (38-90%) Elevated (40-75%) Elevated (100%) Elevated (69%) Elevated (25%)
Cataract Present in 28-35%, later in onset Present in 27-30%, later in onset 23%, later in onset 75%, later in onset At the time of presentation (47%)
Glaucoma Present in 18-54% Present in 30-40% 23% 36%
Vitritis 43% 83% 0% 9% Very rare Always present