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Uveitis (Intraocular Inflammation)

Inflammation of the uveal tract (iris, ciliary body, choroid) classified anatomically as anterior, intermediate, posterior, or panuveitis, with infectious (HSV, VZV, toxoplasmosis, tuberculosis) and non-infectious (HLA-B27 spondyloarthritis, sarcoidosis, Behçet, juvenile idiopathic arthritis) etiologies; managed with topical/oral/intraocular steroids, immunomodulators, biologics (adalimumab), and treatment of the underlying cause to prevent vision-threatening complications.

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Written by: Saygı Hospital Health Guide Editorial Board
Last updated:

This content has been compiled by the Saygı Hospital Health Guide Editorial Board and is periodically reviewed by a specialist physician.

References (5)

This content is for informational purposes only and does not constitute medical advice. You can book an appointment at our Göz Hastalıkları department. Book Appointment →

What is Uveitis (Intraocular Inflammation)?

Uveitis denotes inflammation of the uveal tract—iris, ciliary body, and choroid—and adjacent structures (retina, vitreous, sclera). Standardization of Uveitis Nomenclature (SUN) classifies uveitis anatomically: anterior uveitis (iris/ciliary body, ~60%), intermediate uveitis (vitreous), posterior uveitis (retina/choroid), and panuveitis (all segments). Etiologies include infectious (herpetic HSV/VZV/CMV, toxoplasmosis, tuberculosis, syphilis, Lyme), immune-mediated systemic disease (HLA-B27 spondyloarthritis, sarcoidosis, Behçet disease, juvenile idiopathic arthritis, multiple sclerosis, Vogt-Koyanagi-Harada, sympathetic ophthalmia), and idiopathic (~30-50%). Uveitis accounts for 10-15% of legal blindness in working-age adults globally.

Clinical presentation varies: acute anterior uveitis (HLA-B27, idiopathic) presents with painful red eye, photophobia, and blurred vision with classic 'cells and flare' on slit lamp examination, keratic precipitates, posterior synechiae, and possibly hypopyon (Behçet). Intermediate uveitis presents with floaters and decreased vision from vitritis, vitreous snowballs, and pars plana snowbanking. Posterior uveitis manifests as floaters, scotoma, and decreased vision with retinal/choroidal lesions on fundoscopy and OCT. Workup is etiology-driven: laboratory (CBC, ACE, lysozyme, ANA, HLA-B27, RPR/FTA-ABS, QuantiFERON, Lyme), imaging (chest CT for sarcoid/TB, MRI for MS), and ocular tests (OCT for macular edema, fluorescein angiography, ultrasound).

Treatment is etiology- and severity-driven. Anterior uveitis: topical corticosteroids (prednisolone acetate 1% q1-2h tapered), cycloplegic (cyclopentolate, atropine) for pain and synechiae prevention; for severe cases, periocular triamcinolone or systemic steroids. Intermediate/posterior/panuveitis: systemic corticosteroids (oral prednisone, IV methylprednisolone for severe); steroid-sparing immunomodulators (methotrexate, mycophenolate mofetil, azathioprine, cyclosporine) for chronic disease or steroid-dependent cases; biologics (adalimumab approved for non-infectious uveitis, infliximab for Behçet); intraocular dexamethasone (Ozurdex) or fluocinolone (Yutiq, Iluvien) implants. Infectious uveitis requires specific antimicrobial therapy (acyclovir/valacyclovir for herpetic, pyrimethamine-sulfadiazine for toxoplasmosis, RIPE for TB, penicillin for syphilis). Complications—cataract, glaucoma, macular edema, posterior synechiae, band keratopathy, retinal detachment—require coordinated management.

Symptoms

Eye pain, redness, and photophobia (anterior)
Blurred vision and floaters (intermediate/posterior)
Decreased vision and scotoma
Hypopyon (severe anterior uveitis, classic in Behçet)
Cells and flare on slit lamp examination
Keratic precipitates and posterior synechiae
Retinal/choroidal lesions on fundoscopy

Risk Factors

HLA-B27 positivity (ankylosing spondylitis, reactive arthritis)
Sarcoidosis, Behçet disease, juvenile idiopathic arthritis
Tuberculosis, syphilis, herpetic infection exposure
Multiple sclerosis (intermediate uveitis)
Toxoplasmosis (congenital or acquired)
Recent ocular trauma or surgery (sympathetic ophthalmia)
Family history of autoimmune disease

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Painful red eye with photophobia
  • Sudden floaters or vision decrease
  • Persistent or recurrent eye redness with vision changes
  • Known systemic autoimmune disease with eye symptoms
  • Recent infection with ocular involvement
  • Failure of response to topical steroids
  • Suspected uveitis complications (cataract, glaucoma, macular edema)

Treatment Methods

01
Topical corticosteroids (prednisolone acetate 1%) for anterior uveitis
02
Cycloplegics for pain and synechiae prevention
03
Systemic corticosteroids for intermediate/posterior/panuveitis
04
Steroid-sparing immunomodulators (methotrexate, mycophenolate)
05
Biologics (adalimumab, infliximab) for refractory non-infectious cases
06
Intraocular dexamethasone (Ozurdex) or fluocinolone implants
07
Etiology-specific antimicrobial therapy for infectious uveitis

Which Department to Visit?

You can visit our Göz Hastalıkları department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

Learn About Göz Hastalıkları Department

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