nongranulomatous uveitis
Quick Summary
Nongranulomatous uveitis is a type of eye inflammation affecting the uvea, the middle layer of the eye. It is characterized by an acute onset, often causing pain and intense sensitivity to light. This condition typically has a better recovery rate compared to granulomatous uveitis.1
Nongranulomatous uveitis can be associated with certain viral infections like herpes simplex and herpes zoster, as well as Lyme disease and trauma. It may also occur in individuals with autoimmune diseases linked to human leukocyte antigen B27 (HLA B27), such as ankylosing spondylitis, inflammatory bowel disease, psoriatic arthritis, and Reiter syndrome. Chronic forms of nongranulomatous uveitis are often linked to juvenile idiopathic arthritis or Fuchs heterochromic iridocyclitis.1
Treatment for uveitis generally involves corticosteroids and pupil-dilating drugs, though other immunosuppressants may be used if corticosteroids are ineffective or cause significant side effects. Prompt examination by an eye doctor is crucial, as untreated uveitis can lead to permanent vision damage.1
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