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1 Fuchs Endothelial Dystrophy

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126 Herpes Simplex Keratitis and Related Syndromes<br />

7<br />

Fig. 7.4 Geographic ulcer. Note large corneal ulcer stained with fluorescein that is<br />

geographic in shape (Reprinted with permission from [80])<br />

Patientswithmarginalorlimbalherpeticulcers<br />

are often more symptomatic and less responsive to<br />

treatment [139, 206]. Although epithelial disease<br />

usually resolves, sequelae may ensue such as a<br />

punctate epithelial keratopathy, recurrent corneal<br />

erosions or epithelial granularity. Some degree of<br />

anterior stromal reaction is common underlying<br />

the epithelial lesions and probably represents<br />

an immune response to the epithelial disease<br />

rather than stromal viral invasion. Herpetic<br />

ulcers may become secondarily infected with<br />

bacteria with associated features. A decrease<br />

in corneal sensation is more common than<br />

has previously been realized and neurotrophic<br />

keratopathy may occur as a result of impaired<br />

corneal innervation. This may manifest as loss<br />

of corneal luster and irregularity of the corneal<br />

surface. Punctate epithelial erosions may develop<br />

and progress to a persistent epithelial or<br />

metaherpetic ulcer, also known as an indolent<br />

or trophic ulcer. The ulcer is oval, shallow,<br />

with smooth borders of grey, elevated, thickened<br />

and rolled epithelium [17, 69, 100].<br />

7.5.7 Stromal Keratitis<br />

Herpetic stromal disease accounts for 2% of initial<br />

presentations and 20–48% of recurrent her-<br />

petic disease [42, 99, 128]. It results from viral<br />

invasion of the stroma, either from reactivation<br />

of latent virus in the supplying sensory nerves or<br />

from within the cornea itself.<br />

The associated immune response contributes<br />

to the type of stromal disease seen. There may be<br />

no history of previous infectious epithelial keratitis<br />

and the epithelium is usually intact. The main<br />

characteristic is stromal inflammation, which<br />

may be focal, multifocal or diffuse and may be associated<br />

with anterior uveitis [205]. The inflammation<br />

may be chronic, recurrent or recrudescent<br />

leading to stromal scarring, thinning, neovascularization,<br />

and lipid deposition (Fig. 7.5).<br />

Occasionally, a partial or complete immune<br />

ring, similar to a Wessely ring, is seen in the central<br />

or paracentral mid-stroma [115]. As with<br />

epithelial disease, marginal keratitis or limbitis<br />

tends to be associated with a greater inflammatory<br />

or immune response. Stromal neovascularization<br />

can be sectoral or diffuse and frequently<br />

occurs in several layers of the cornea, a condition<br />

described as “interstitial stromal HSV keratitis”<br />

[100]. Necrotizing stromal keratitis may occur.<br />

There is necrosis, ulceration, and dense infiltration<br />

of the stroma, usually with an overlying<br />

epithelial defect. Grayish white homogeneous<br />

abscesses with edema, keratic precipitates, and<br />

iridocyclitis are seen.

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