Diagnosis → Ophthalmology

Iridocyclitis

Inflammation of the anterior chamber involving the iris and ciliary body.

Also known as: AAU, Acute anterior uveitis, Anterior cyclitis, Anterior uveitis, Iritis

Etiology

Cause [nce][tdb][fvd]

Pathophysiology [nce][fvd][qho]

  1. Trigger and loss of ocular immune privilege

    • Infection

    • Autoimmunity

    • Immune-modulating drugs disrupt ocular immune privilege mechanisms (e.g., local immunosuppressive milieu in aqueous humor)

  2. Breakdown of the blood–aqueous barrier

    • Increased vascular permeability in iris/ciliary body → protein exudation and leukocyte trafficking

  3. Anterior chamber inflammatory cascade

    • Inflammatory cells/protein in aqueous humor → pain, photophobia, redness, hypopyon

  4. Structural sequelae from ongoing/recurrent/chronic inflammation

    • Synechiae

    • Cataract

    • Secondary glaucoma/ocular hypertension

    • Macular edema

Risk factors [nce][tdb][fvd]

Complications [nce][fvd]

Epidemiology

Incidence per 100.000 [6sm][9vk]

Default

Epidemiology chart for Incidence

Symptoms & findings

Symptoms

Blurred vision, Keratic precipitates, Lacrimation, Miosis, Photophobia, Red eye, Synechia, Vitreous opacities

Clinical findings

ANA, Elevated CRP, Elevated Sedimentation Rate, HLA-B27, Hypopyon

Anamneses

None listed.

Localized findings

Pain
Radiates
EyesRegio orbitalis
Onset
Acute (minutes)Subacute (hours)Gradual (days)
Pattern
Constant
Quality
Aching
Severity
Mild (1-3)Moderate (4-7)

Approach

Approach [nce][tdb][fvd]

Treatment

  1. Topical corticosteroid: Prednisolone 1% (taper over weeks guided by AC cells) [nce]

  2. Cycloplegic Atropine 1%: Dilate the pupil, pain control, prevent/break synechiae

  3. Intraocular pressure management

  4. Refractory or high-risk disease: if inadequate control with topical therapy

    • Periocular/intraocular corticosteroid if complications

    • Systemic corticosteroids or vitreous implants for severe, bilateral, recurrent, or posterior spillover disease

    • Steroid-sparing systemic immunomodulatory therapy

  5. HLA-B27–associated (SpA-associated)

    • If frequent recurrences/severe disease --> biologic DMARDs (anti-TNF, IL-6)

  6. Viral anterior uveitis (HSV/VZV/CMV)

    • Add systemic antiviral therapy

  7. Immune checkpoint inhibitor–associated anterior uveitis

    • Severe cases may require systemic corticosteroids and prompt discontinuing ICI per oncology guidance

    • Methotrexate can be considered if poor response to systemic steroids

Differential diagnoses

Conjunctivitis, Corneal abrasion, Corneal ulcer, Endophthalmitis, Episcleritis, Foreign body, Glaucoma, Keratitis, Lymphoma, Retinitis, Scleritis, Subconjunctival hemorrhage, Trauma


References

[1] Gurnani B, Kim J, Tripathy K, et al. Iritis. [Updated 2023 Aug 25]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK430909/

[2] Chang EL, et al. Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitors. J Immunother Cancer. 2025.

[3] Maghsoudlou P, Epps SJ, Guly CM, Dick AD. Uveitis in Adults. JAMA. 2025. . 11.3 Gelfman S, et al. A large meta-analysis identifies genes associated with anterior uveitis. Nat Commun. 2023.

[4] Pan S, et al. Beyond the joints: mechanistic insights and multidisciplinary strategies for spondyloarthritis-associated uveitis. Front Immunol. 2025.

[5] Xu, T. T., Reynolds, M. M., Hodge, D., & Smith, W. (2021). Epidemiology of Uveitis in Olmsted County, Minnesota: A Population-Based Follow-Up Study. Ocular immunology and inflammation, 31, 112 - 118.

[6] Acharya NR, Tham VM, Esterberg E, et al. Incidence and Prevalence of Uveitis: Results From the Pacific Ocular Inflammation Study. JAMA Ophthalmol. 2013;131(11):1405–1412.

Scroll to top