HIV-related
eye disease can be classified as
retinal HIV microangiopathy,
opportunistic infections, neuro-ophthalmic manifestations and unusual
malignancies. There is a 52-100% lifetime accumulative risk of HIV patients developing eye problems. Seventy-seven per cent of patients with ocular manifestations of HIV had CD4 counts < 200 cells/μL. Cytomegalovirus (CMV) is the most prevalent
opportunistic infection, however, Africa has a low incidence of this, and more commonly
squamous cell carcinoma, compared to the western hemisphere. Due to
highly active antiretroviral therapy (
HAART), the anti-CMV
therapy may be discontinued if the CD4+ T cell count is > 100 cells/μL for a minimum of three months. Despite
HAART, patients with a CD4 count < 50 cells/μL have a similar risk of developing CMV
retinitis as compared to the pre-
HAART era.
Opportunistic infections include CMV, herpetic retinopathy (progressive outer
retinal necrosis - PORN), less commonly
toxoplasmosis, pneumocystis and cryptococcus.
Malignancies associated with HIV include
Kaposi's sarcoma and conjunctival
squamous cell carcinoma.
Cranial nerve palsies, optic disc swelling and
atrophy are characteristic neuro-ophthalmic features. They usually occur secondary to
meningitis/
encephalitis (from cryptococcus and
tuberculosis). With the advent of
HAART, new complications have developed in CMV
retinitis: immune recovery
uveitis (IRU) and cystoid macula oedema (CMO). Immune recovery
uveitis occurs in 71% of patients if
HAART is started before the induction of the anti-CMV treatment. However, this is reduced to 31% if
HAART is started after the induction treatment.
Molluscum contagiosum and
Kaposi's sarcoma can spontaneously resolve on
HAART. Highly active anti-retroviral
therapy has reduced the frequencies of
opportunistic infections and improved the remission duration in HIV patients.