Uveitis

Anterior uveitis

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75-90% of all cases of uveitis

All patients must have a dilated fundus examination

Idiopathic AAU

  • 50% of AAU occurs in isolation
  • Biphasic: ages 30 and 60
  • M=F
  • Typically unilateral

Clinical features

  • Pain
  • Photophobia
  • Circumlimbal injection
  • KPs
  • AC flare/cells
  • Posterior synechiae
  • Spillover anterior vitreous cells

Management

  • Frequent topical corticosteroids
  • Mydriasis: acutely to break PS
  • Consideration of oral steroid if not responding within 48 hours

HLA-associated AAU

  • 55% of AAU patients are HLA-B27 positive (8% of general population) rising to 70% of those with recurrent episodes

    • However, only 1% of HLA-B27 positive patients develops AAU
    • 84% of HLA-B27 positive patients with AAU have other systemic disease
  • M>F

  • Peaks age 30

  • Associated with positive family history

  • Associated with

    • Reiter’s disease
    • Ankylosing spondylitis
    • Psoriatic arthritis
    • IBD:
      • IBD patients with sclerouveitis are more likely to be HLA-B27 negative and more likely to have RA-pattern arthritis rather than sacroilitis
  • Anterior segment inflammation typically more severe than idiopathic AAU

    • Fibrin is a more common feature
    • Hypopyon and PS more common
    • Late CMO may develop
    • Recurrence is more likely
  • Management is as for AAU

Seronegative spondyloarthropathies

  • Inflammatory arthritides affecting the synovium and extra-articular sites
  • Typically an asymmetrical arthritis
  • Strongly associated with HLA-B27
  • Ankylosing spondylitis
    • Affects the spine and sacro-iliac joints
    • M>F
    • 25% develop anterior uveitis
    • anti-TNF drugs may reduce recurrences
    • 9% develop intractable uveitis
    • Alternating/’flip-flopping’ uveitis

Psoriatic arthritis

  • 10% develop ophthalmic disease: conjunctivitis (self-limiting), keratitis (peripheral corneal infiltrates), uveitis (which is atypical in that it may present bilaterally)
  • Psoriatic arthritis is usually benign mut a minority develop arthritis mutilans which is destructive
  • IBD-related: 5% develop anterior uveitis. Rarely epi/scleritis or retinal vasculitis
  • Reiter’s syndrome: reactive arthritis, urethritis and conjunctivitis
    • Associated with non-gonococcal STI: chlamydia, yersinia, salmonella, shigella
    • 70% are HLA-B27 positive
    • Bilateral mucopurulent conjunctivitis (self-limiting)
    • Punctate corneal epitheliopathy
    • AAU (12%)
    • Aortic incompetence is a rare life-threatening complication

Anterior uveitis syndromes

Fuch’s heterochromic cyclitis

  • Chronic non-granulomatous anterior uveitis
  • Unknown cause: may be associated with rubella
  • F=M
  • Unilateral in 90%
  • Clinical features
    • White eye
    • Floaters
    • Glare
    • Asymptomatic
    • Iris atrophy: moth-eaten, transillumination defects, abnormal iris vessels, iris heterochromia, iris nodules (Koeppe > Busacca)
    • No PS
    • PSCO
    • Vitreous opacities
    • Raised IOP: rarely secondary glaucoma
    • Gonioscopy: open angles, twig-like vessels in the angle (occasionally cause hyphaema on paracentesis)

Tubulo-interstitial nephritis and uveitis (TINU)

  • Typically affects young females

  • Bilateral nongranulomatous anterior uveitis

  • Associated with HLA-DQ and HLA-DR14

  • Idiopathic or associated with medication or infection

    • NSAIDs, penicillin, furosemide
    • Strep and staph infections
  • Acute renal failure: typically recovers but occasionally some chronic impairment

  • Associated systemic illness

    • Creatinine and ESR are raised
    • Increased beta-2 microglobulin in urine
  • Renal biopsy is indicated: oedema in the renal interstitium with mononuclear infiltrate

  • Most patients recover normal renal function and VA with treatment (systemic steroid)

IgA-nephropathy

  • Micro- or macroscopic haematuria associated with respiratory tract infections

Kawasaki’s disease

  • Acute vasculitis in children

  • >5 days of fever with

    • Conjunctival injection
    • Rash
    • Desquamation of the extremities
    • Cervical lymphadenopathy
    • Mucosal changes (pharyngeal injection, cracked red lips, strawberry tongue)
  • AAU develops in the first week of illness

  • Coronary artery aneurysms develop in 20%

Others

  • Posner Schlossman syndrome: see also Glaucoma section
  • Anterior segment ischaemia
    • May be associated with OIS (look for irregular/attenuated retinal vessels)
  • Schwartz-matsuo syndrome: see Glaucoma section
    • Associated with large, mac-off detachments

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