Herpes Simplex Epithelial Keratitis
Herpes simplex virus (HSV) is a very common, lifelong infection that often is asymptomatic. In the 2015-2016 National Health and Nutrition Examination Survey, the prevalence of HSV type 1 (HSV-1) was 47.8% and HSV type 2 (HSV-2) was 11.9%.  Globally, the incidence of HSV keratitis is 1.5 million yearly, including 40,000 new cases that result in severe visual impairment.  In the United States, approximately 500,000 people have afflicted with ocular HSV. Ocular manifestations of HSV- I and HSV- II include blepharoconjunctivitis, epithelial keratitis, stromal keratitis (necrotizing or non-necrotizing), iridocyclitis, and/or acute retinal necrosis.
This EyeWiki article will focus on the corneal epithelial manifestations of HSV. Descriptions of the HSV stromal and endothelial manifestations can be found here.
Herpetic keratitis can be unilateral or, more rarely, bilateral. The latter being more common in patients with atopy due to proposed immune dysregulation increasing susceptibility to viral infections. Age, geographic location, and socioeconomic status appear to affect the prevalence of disease. HSV can affect all layers of the cornea, and may be accompanied by a blepharoconjunctivitis, which may result in lesions of the eyelids and a follicular response of the conjunctiva. Characteristically, HSV epithelial keratitis presents with classic dendritic lesions with terminal bulbs. Recurrent activations within the sensory ganglion can result in cornea scarring, necrosis, and decreased sensation (neurotrophic cornea).
HSV keratitis is caused by the herpes simplex virus, a double- stranded DNA virus made up of an icosahedral shaped capsid surrounding a core of DNA and phosphoproteins of viral chromatin. HSV- I and HSV- II are differentiated by virus specific antigens. HSV- I typically affects the orofacial region whereas HSV- II usually causes genital infections, though studies have shown that both viruses may affect either location.
Risk factors for development of primary HSV involve direct contact with infected secretions or lesions.
- Trigeminal nerve manipulation
- Infectious disease and immunocompromised states.
- COVID-19 infection
- COVID-19 vaccination
Corneal scrapings of HSV keratitis prepared with Giemsa stain may reveal the presence of intranuclear viral inclusion bodies. Multinucleated giant cells may also be found. With complete stromal inflammation, a granulomatous reaction may be seen, usually at the level of Descemet's membrane.
Ocular herpetic disease is more frequently caused by HSV- I, which is presumed to gain access to the cornea via the trigeminal nerve from an oral infection or direct contact of infected secretions. Initial infection typically remains asymptomatic, but patients may present with an acute follicular conjunctivitis and an upper respiratory infection. After the primary infection, the virus travels via sensory nerve axons to establish a latent infection in the trigeminal ganglion where it resides permanently. The virus is then capable of reactivation along any branch of the trigeminal nerve to cause ocular morbidity.
Prevention of herpetic infection includes avoidance of direct contact with lesions and secretions of a patient with active HSV.
Key aspects to inquire about in the history of patients with suspected HSV include past infections (history of recurrent "red eye", particularly unilateral), underlying systemic diseases, immunosuppression or immunocompromised state, history of eyelid lesions, and history of oral and genital ulcers.
In addition to a standard biomicroscopy, special attention should be paid to the presence of a preauricular lymph node, vesicular lesions on the lids or adnexa, bulbar follicles, decreased corneal sensation, and most notably the presence of epithelial dendrites on the cornea.
For primary HSV keratitis, it is more common for patients to present with a blepharoconjunctivitis than with cornea involvement. However, diffuse punctate keratopathy or corneal microcysts may be visible.
Recurrent HSV keratitis can present as epithelial keratitis. The earliest sign of epithelial disease include raised clear vesicles that later coalesce to form the classic dendritic lesion. The dendritic ulcer, the dichotomous branching cornea lesion, can be stained with fluorescein and is the hallmark of HSV epithelial keratitis. These epithelial lesions represent active replicating virus. As the dendritic ulcer may evolve into a geographic ulceration of the cornea, especially in patients with compromised immunity or on topical steroids.
The hallmark of HSV keratitis is the presence of multiple small branching epithelial dendrites on the surface of the cornea, although often times it first presents as a coarse, punctuate epithelial keratitis, which may be mistaken for a viral keratitis. The HSV dendrite possesses terminal bulbs that distinguish it from the herpes zoster pseudodendrite and follows the nerve pattern of the cornea.
Typically, patients with acute HSV keratitis present with blurred vision, photophobia, pain, redness, and/or tearing.
The clinical diagnosis of HSV may be suggested by the presence of the multiple arborizing dendritic epithelial ulcers with terminal bulbs. The bed of the ulcer stains with fluorescein, while the swollen corneal epithelium at the edge of the ulcer typically stains with rose bengal. Several dendrites may also coalesce to form a geographic epithelial ulcer. In addition, there may be mild conjunctival injection, ciliary flush, mild stromal edema and subepithelial white blood cell infiltration. Following resolution of the primary infection, a "ghost dendrite" may be visible just beneath the prior area of epithelial ulceration.
The diagnosis of HSV is often made clinically, however, laboratory tests are available to confirm the diagnosis in difficult cases (and in all cases of neonatal herpetic infection). Serologic testing may be performed but is usually not helpful in recurrent disease as most adults are laterally infected with HSV. However, conjunctival scrapings, impression cytology specimens, and scrapings from vesicular lesions on the skin may be tested by cytology, culture, or polymerase chain reaction (PCR) for the presence of HSV. Fluorescent antibody (FAB) testing involving impression cytology using nitrocellulose membrane or a cornea smear. A Tzanck smear can reveal multinucleated giant cells and intranuclear eosinophilic inclusion bodies. Serum antibody testing is typically of limited use.
See Diagnostic Procedures
The differential diagnoses of HSV include herpes zoster ophthalmicus, viral keratitis (usually adenovirus), neurotrophic keratopathy, epithelial regeneration line, iatrogenic (topical drops such as antivirals), acanthamoeba keratitis, soft contact lens overwear, microbial keratitis, staphylococcal marginal keratitis, and Thygeson’s superficial punctuate keratitis.
Primary HSV epithelial keratitis usually resolves spontaneously, however, treatment with antiviral medication does indeed shorten the course of the disease and may therefore reduce the long- term complications of HSV.
The mainstay of therapy is antiviral treatment either in the form of oral administration of acyclovir or valacyclovir or famciclovir for 10 to 14 days or topical antiviral medications. Topical ganciclovir 0.15% can also be utilized and is approved by the FDA for the treatment of acute herpetic keratitis since 2009. It is typically dosed five times a day until the cornea ulcer heals, and then three times a day for another week. Topical therapy with trifluridine 1% eight to nine times a day can also be prescribed, but care must be taken to ensure antiviral drops are discontinued within 10-14 days due to significant corneal toxicity. Topical acyclovir is not approved by the FDA, but used commonly outside the United States for the treatment of HSV epithelial keratitis. Topical steroids are contraindicated in the presence of active epithelial disease, although cycloplegia drops and topical antibiotics may be added.
Epithelial debridement of the dendrites may also be utilized in conjunction with antiviral therapy to help reduce viral load. Amniotic membrane may promote epithelial healing and reduce scar formation in conjunction with antivirals. According to the Herpetic Eye Disease Study (HEDS), long- term prophylaxis with oral antivirals may decrease the risk of recurrent HSV keratitis.
Medical follow up
The patient should be closely monitored and if no response to treatment occurs after one week of therapy, the possibility of resistance to antiviral therapy, antiviral toxicity, neurotrophic disease, poor compliance with medication and/or an alternative diagnosis should be considered.
If there is visually significant stromal scarring, a penetrating keratoplasty may be performed once the disease is quiescent. Depending on the location and size of the scar, a lamellar keratoplasty may also be used to clear the visual axis. Of note, in eyes that are unable to sustain a clear graft, a Boston keratoprosthesis may be a viable option.
Surgical follow up
Follow-up should be performed as standard of practice for penetrating keratoplasty. Special attention should be paid to signs of recurrence of herpetic disease. Oral antiviral therapy may improve the rate of graft survival by decreasing the number of recurrences.
Corneal complications of herpetic eye disease range from epitheliopathy to frank neurotrophic or metaherpetic ulcers. Long standing disciform keratitis may also result in bullous keratopathy. Late complications of deep vascular stromal scarring include secondary lipid keratopathy. Finally, stromal inflammation may lead to visually significant corneal scarring and irregular astigmatism.
Prognosis is usually good, but greatly varies depending on severity and number of recurrences of the disease.
Region Specific Information (from the AAO's Global Ophthalmology Guide):
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