Pars planitis is a rare inflammatory condition that affects the eye, specifically the pars plana region of the eye's ciliary body. This condition primarily affects young adults and is characterized by inflammation in the gel-like substance (vitreous) that fills the eye.
Symptoms: Individuals with pars planitis may experience floaters, blurred vision, light sensitivity, and eye pain. In some cases, inflammation can spread to other parts of the eye, leading to complications such as cataracts, glaucoma, or retinal detachment.
Causes: The exact cause of pars planitis is unknown, but it is believed to be an autoimmune disorder where the body's immune system mistakenly attacks the eye tissues. It may also have a genetic component.
Diagnosis and Treatment: Diagnosis of pars planitis involves a comprehensive eye examination, including an assessment of the vitreous and retina. Treatment aims to reduce inflammation and manage symptoms. This may involve the use of corticosteroid eye drops, oral medications, or immunosuppressive drugs. In severe cases, surgical intervention may be necessary.
Prognosis: Pars planitis is a chronic condition that can have varying outcomes. While some individuals may experience mild symptoms that improve over time, others may require ongoing treatment to manage inflammation and prevent complications.