Uveitis: Causes and symptoms

The causes of uveitis are not fully understood, but they can be a result of trauma, allergy, or a response to a systemic or ocular disease. Uveitis may be a type of immune-response mechanism. In people with impaired immune systems, uveitis may be due to an infection.

Chronic uveitis is often associated with systemic disorders (e.g., Lyme disease, sarcoidosis, or juvenile rheumatoid arthritis).

The so-called classic symptoms of anterior uveitis— severe pain; redness, particularly around the edge of the iris; and extreme sensitivity to light (photophobia)— occur mostly in acute uveitis. In anterior uveitis, the doctor will see a so-called "flare and cell" pattern when looking into the watery fluid (aqueous humor) between the cornea and the lens of the patient's eye. The iris may adhere to the lens, thus increasing the intraocular pressure. There may be nodules on the iris. There may be tearing and the pupil may be constricted and nonreactive. In severe cases of anterior uveitis, there may be hypopyon (a small amount of pus or collection of white cells) visible when the doctor examines the eye.

GRANULOMATOUS UVEITIS. In granulomatous uveitis, there will be large yellowish-white cells visible on the back of the cornea, and possibly some small nodules on the iris. Granulomatous uveitis is usually less acute than the nongranulomatous form; the eye is only mildly inflamed and the patient's vision is somewhat blurred.

Granulomatous uveitis can be produced by syphilis, toxoplasmosis, cytomegalovirus, sarcoidosis, tuberculosis, or Vogt-Koyonagi-Harada syndrome (VKH). VKH is marked by severe uveitis associated with hair loss, hearing loss, loss of pigment in the eyelashes and brows, and headaches. It occurs most commonly in Asians.

NONGRANULOMATOUS UVEITIS. In nongranulomatous uveitis, the cells visible on the cornea are smaller, and there are no masses on the iris. This type of anterior uveitis is, however, more painful. The eye is red and the patient experiences both photophobia and loss of vision.

Systemic diseases that can cause nongranulomatous uveitis include ankylosing spondylitis, Reiter's syndrome, psoriasis, ulcerative colitis, Behcet's syndrome, Lyme disease, and Crohn's disease. Children— especially girls—with anterior uveitis should be screened for juvenile rheumatoid arthritis (JRA).

The symptoms of posterior uveitis are sometimes subtle. The patient may notice blurred or hazy vision, or floating black spots before the eyes. There may be pain and photophobia. The iris may attach to the lens in the eye thus increasing intraocular pressure.

Posterior uveitis may be acute or chronic. It is more likely to involve both eyes. When the doctor examines the eye, cells may be seen in the vitreous humor, which is the normally transparent gel that fills the eyeball behind the lens. There will be yellowish or dark areas of inflammation on the choroid and the retina. The blood vessels in the retina develop a sheath or covering of inflammatory tissue. In severe cases, the vitreous humor is so cloudy that the doctor cannot see the retina at the back of the eye.

PARS PLANITIS. Pars planitis is an inflammation of the pars plana, which is a part of the ciliary body. Pars planitis usually occurs in older children or young adults, and can develop into posterior uveitis.

The diseases that cause granulomatous uveitis may also cause posterior uveitis.

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