EENT · PANCE / PANRE

Anterior Uveitis (Iritis)

Painful red eye with photophobia, miotic pupil, and cells/flare in the anterior chamber; treat with cycloplegic and topical steroid; investigate for HLA-B27 disease.

Also known as: anterior uveitis, iritis, iridocyclitis, acute anterior uveitis, HLA-B27 uveitis

Overview

Inflammation localized primarily to the anterior segment of the uveal tract — the iris (iritis) and ciliary body (iridocyclitis). Classified by onset (acute, recurrent, chronic), laterality, and granulomatous vs nongranulomatous appearance. Most common form of uveitis (about 75% of cases).

Epidemiology

Incidence 8-12 per 100,000 per year. Peak age 20-50, slight male predominance. HLA-B27 is positive in about 50% of acute anterior uveitis cases; the lifetime risk in HLA-B27 carriers is 1-2%.

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Question 1EENTMedium
A 28-year-old man presents with a 2-day history of a painful, red right eye with photophobia and blurred vision. He reports a dull brow ache and says bright light makes the pain worse. He has had a similar episode in the same eye a year ago and notes several months of low back stiffness that improves with activity. On examination, visual acuity is mildly reduced. There is perilimbal redness with deeper vessel injection, and the pupil is small and slightly irregular. Slit-lamp examination shows cells and flare in the anterior chamber with fine keratic precipitates on the corneal endothelium. Fluorescein staining is negative. Which of the following is the most likely diagnosis?
  • AHerpes simplex keratitis
  • BAngle-closure glaucoma
  • CBacterial conjunctivitis
  • DAcute anterior uveitis
Reveal answer & full explanation
Correct answer: D — Acute anterior uveitis
  • AHerpes simplex keratitis
  • BAngle-closure glaucoma
  • CBacterial conjunctivitis
  • DAcute anterior uveitis

Why Acute anterior uveitis is correct

  • The triad of a painful red eye with photophobia, ciliary (circumlimbal) flush, and a miotic, slightly irregular pupil from ciliary spasm is the classic anterior uveitis presentation.
  • Cells and flare in the anterior chamber on slit-lamp exam are diagnostic, and fine (nongranulomatous) keratic precipitates on the corneal endothelium support the diagnosis. No cells, no uveitis.
  • Recurrent unilateral acute anterior uveitis in a young man with inflammatory low back pain that improves with activity points to HLA-B27-associated disease (ankylosing spondylitis spectrum).

Why the others are wrong

  • Angle-closure glaucoma causes severe pain with headache, nausea, and halos, a fixed mid-dilated pupil, corneal edema, and markedly elevated intraocular pressure; the small, irregular pupil and anterior-chamber cells here argue against it.
  • Herpes simplex keratitis produces a dendritic corneal lesion that stains with fluorescein and reduced corneal sensation, but fluorescein staining is negative here.
  • Bacterial conjunctivitis causes purulent discharge and a papillary conjunctival reaction with a normal pupil, no anterior-chamber cells, and no true photophobia.
Question 2EENTMedium
A 29-year-old man presents with 2 days of aching pain, redness, and light sensitivity in his right eye, along with blurred vision. He reports a similar episode in the same eye last year and has had intermittent low back pain that improves with exercise. Visual acuity is mildly reduced on the right. Examination shows perilimbal redness and a small, somewhat irregular pupil. Intraocular pressure is normal, and fluorescein staining shows no corneal epithelial defect. Which of the following additional findings is most likely on examination?
  • AA branching dendritic lesion that stains with fluorescein
  • BLeukocytes and protein layered in the anterior chamber
  • CA fixed mid-dilated pupil with elevated intraocular pressure
  • DA follicular conjunctival reaction with a watery discharge
Reveal answer & full explanation
Correct answer: B — Leukocytes and protein layered in the anterior chamber
  • AA branching dendritic lesion that stains with fluorescein
  • BLeukocytes and protein layered in the anterior chamber
  • CA fixed mid-dilated pupil with elevated intraocular pressure
  • DA follicular conjunctival reaction with a watery discharge

Why Leukocytes and protein layered in the anterior chamber is correct

  • Anterior uveitis is a clinical diagnosis confirmed on slit-lamp examination: breakdown of the blood-aqueous barrier lets leukocytes (cells) and protein (flare) leak into the anterior chamber, and this is the defining finding.
  • The recurrent, unilateral, painful red eye with ciliary (perilimbal) flush, a small irregular pupil, and inflammatory back pain that improves with exercise fits HLA-B27-associated acute anterior uveitis, which warrants HLA-B27 testing and rheumatology referral.

Why the others are wrong

  • A fixed mid-dilated pupil with elevated intraocular pressure describes acute angle-closure glaucoma; here the pupil is small (miotic from ciliary spasm) and the intraocular pressure is normal.
  • A branching dendritic lesion that stains with fluorescein defines herpes simplex keratitis; fluorescein staining showed no epithelial defect, excluding it.
  • A follicular conjunctival reaction with a watery discharge points to viral conjunctivitis, which causes minimal pain and no true photophobia or anterior chamber cells.
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Risk factors

  • HLA-B27 positivity
  • Ankylosing spondylitis, reactive arthritis, psoriatic arthritis, IBD-associated arthritis
  • Juvenile idiopathic arthritis (especially ANA-positive oligoarticular form)
  • Sarcoidosis, tuberculosis, syphilis, herpesvirus infection (HSV, VZV, CMV)
  • Behcet disease
  • Ocular trauma, recent intraocular surgery (sterile postoperative uveitis)
  • Idiopathic (about one-third of cases)

Pathophysiology

Breakdown of the blood-aqueous barrier permits leukocyte and protein leak into the anterior chamber. Inflammatory mediators released by ciliary body and iris produce ciliary spasm (pain, miosis, photophobia), exudation of cells (cells in AC) and protein (flare), and may deposit on the corneal endothelium (keratic precipitates). Chronic or recurrent inflammation causes posterior synechiae (iris adhesions to lens) and secondary glaucoma.

Clinical presentation

Symptoms

  • Unilateral (usually) eye pain, photophobia, blurred vision, tearing
  • Headache or brow ache
  • Reduced visual acuity, often mildly to moderately impaired
  • Recurrent episodes in HLA-B27-related disease — often the SAME eye or alternating
  • Associated systemic features may include low back pain (AS), arthritis, mucosal ulcers, GI symptoms, dermatitis

Signs / physical exam

  • Circumlimbal (ciliary) flush — perilimbal redness with deeper vessel injection
  • Miotic pupil from ciliary spasm; may be irregular if posterior synechiae
  • Slit-lamp: cells and flare in the anterior chamber (graded 1+ to 4+); hypopyon in severe disease (especially Behcet, HLA-B27)
  • Keratic precipitates on the corneal endothelium — fine (nongranulomatous) or mutton-fat large/greasy (granulomatous, suggesting sarcoid, TB, syphilis)
  • IOP may be low (decreased aqueous production from ciliary body inflammation) or elevated (trabeculitis or pupillary block)
  • Posterior synechiae — iris adhesions to anterior lens capsule; pupil shape becomes irregular with dilation

Classic findings

Painful red eye with photophobia, ciliary flush, miotic pupil, and cells/flare on slit-lamp examination.

Differential diagnosis

  • Acute angle-closure glaucoma — Severe pain, headache, nausea, halos around lights; fixed mid-dilated pupil; markedly elevated IOP; corneal edema; emergency
  • Bacterial keratitis — Pain, photophobia, mucopurulent discharge, corneal infiltrate with epithelial defect; fluorescein staining; contact lens user
  • Herpes simplex keratitis — Dendritic corneal lesion on fluorescein; decreased corneal sensation; antiviral therapy
  • Conjunctivitis — Discharge, papillary or follicular reaction, no anterior chamber cells, no photophobia (or mild)
  • Episcleritis / scleritis — Sectoral redness, deep ache (scleritis); scleritis often associated with systemic disease and threatens vision
  • Endophthalmitis — Acute severe pain and vision loss after surgery or trauma; hypopyon, vitritis; emergency
  • Posterior uveitis or panuveitis — Floaters, decreased vision; cells in vitreous; chorioretinal lesions on fundus exam

Diagnostic workup

Diagnostic criteria

Clinical diagnosis by slit-lamp findings (cells and flare in the anterior chamber). Standardization of Uveitis Nomenclature (SUN) grading is used for cell and flare quantification.

Labs

  • First episode of unilateral acute anterior uveitis without systemic features may need NO workup
  • If recurrent, bilateral, granulomatous, or with systemic features: CBC, ESR, CRP, ACE, lysozyme, HLA-B27, RPR/treponemal, QuantiFERON-TB, ANA, urinalysis, Lyme serology if exposure
  • Chest X-ray or CT chest for sarcoid and TB screening
  • Sacroiliac imaging or MRI if back pain to assess for ankylosing spondylitis
  • Anterior chamber tap with PCR (HSV, VZV, CMV) for atypical or chronic cases

Imaging

  • Slit-lamp examination — primary diagnostic modality; documents cells, flare, KPs, synechiae
  • Dilated fundoscopy to assess posterior involvement
  • Anterior segment OCT for monitoring inflammation in select cases
  • Goldmann tonometry — important to monitor for steroid-induced or inflammatory IOP elevation

Diagnostic algorithm

FeatureAnterior uveitisAcute angle-closure glaucomaConjunctivitisBacterial keratitis
PainModerate, deepSevere + headache/nauseaMild grittySevere + photophobia
PupilMiotic / irregularMid-dilated, fixedNormalNormal
CorneaClear ± KPsHazy edematousClearInfiltrate ± epithelial defect
IOPLow, normal, or highMarkedly elevatedNormalNormal
AC cellsPresentMay be presentAbsentMay be present
DischargeNone (tearing)NoneMucoid/purulentMucopurulent
First stepSlit lamp + cycloplegic + topical steroid + ophthoLower IOP + ophthalmology emergencyHygiene ± topical antibioticTopical fluoroquinolone + ophtho
Quick differentiation of the painful red eye.

Treatment

First-line

  • Topical cycloplegic — cyclopentolate 1%, homatropine 5%, or atropine 1% — to relieve ciliary spasm and prevent posterior synechiae
  • Topical corticosteroid — prednisolone acetate 1% every 1-2 hours initially, tapered over weeks; difluprednate 0.05% is an alternative potent steroid
  • Treat underlying cause if identified (antivirals for HSV/VZV uveitis, antibiotics for syphilis, anti-TB for tuberculosis)
  • Urgent ophthalmology referral within 24 hours
  • Monitor IOP at every visit — both inflammatory glaucoma and steroid-induced ocular hypertension can occur

Second-line / adjunct

  • Periocular or intravitreal corticosteroid injection (triamcinolone, dexamethasone implant) for severe or non-responsive disease
  • Systemic corticosteroid for bilateral severe or sight-threatening inflammation
  • Immunomodulatory therapy (methotrexate, azathioprine, mycophenolate, cyclosporine) for chronic recurrent disease
  • TNF-alpha inhibitors (adalimumab is FDA-approved for noninfectious uveitis; infliximab off-label) for HLA-B27-related, JIA-associated, or Behcet uveitis
  • Laser or surgical synechiolysis for refractory synechiae

Complications

  • Posterior synechiae with pupillary block and secondary angle-closure glaucoma
  • Cataract (from inflammation and from chronic steroid use)
  • Glaucoma (inflammatory, steroid-induced, or angle-closure)
  • Cystoid macular edema
  • Band keratopathy in chronic disease
  • Hypotony with phthisis in chronic uncontrolled inflammation
  • Vision loss

PANCE pearls

  • Cells in the anterior chamber on slit-lamp examination clinch the diagnosis — no cells, no uveitis.
  • Always dilate the pupil with a cycloplegic — both for synechiae prevention and to allow posterior segment examination.
  • Recurrent acute anterior uveitis, especially in young men with low back pain, should prompt HLA-B27 testing and rheumatology referral.
  • Granulomatous (mutton-fat) keratic precipitates suggest sarcoid, TB, or syphilis — workup mandatory.
  • Monitor intraocular pressure at every visit; both the inflammation and the steroids can drive glaucoma.
  • Never give topical steroids for a red eye unless cornea has been examined with fluorescein to exclude dendritic HSV keratitis.

References

  • AAO PPP — American Academy of Ophthalmology Preferred Practice Pattern: Uveitis
  • SUN — Standardization of Uveitis Nomenclature (SUN) Working Group recommendations (Jabs et al., Am J Ophthalmol 2005)
  • AUSCON / FOSTER — Foster CS, Kothari S, Anesi SD et al. The Ocular Immunology and Uveitis Foundation preferred practice patterns of uveitis management

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