ant uveitis Flashcards

1
Q

Non-granulomatous

A

acute, painful, red, short, small/fine KP, PMNs, lymphoctes

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2
Q

Granulomatous

A

insidious, less pain, less red, mutton fat KP, nodular lesions, macrophages, giant cells, nodules in AC, long

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3
Q

Pathophysiology of anterior uveitis

A

Breakdown of BAB (tight junctions) due to inflammation of ciliary epithelium and iris capillaries.
Aqueous fills with macromolecules (flare) and cells.

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4
Q

Iris capillaries

A

Non-fenestrated (tight junctions) - endothelial cells

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5
Q

Ciliary body capillaries

A

Stroma- fenestrated
Inner epi - NPE (tight junctions)
Outer epi - PE (gap junctions) - controls aqueous production (uveitis –> decrease IOP)

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6
Q

Signs of acute anterior uveitis (AAU)

A
  • Hyperaemia
  • Cells in AC (= active inflammation)
  • Hypopyon
  • Flare
  • Synechiae (PAS, posterior)
  • KP
  • Miotic pupil (iris sphincter spasm - substance P)
  • Vitreous cells
  • IOP (early: decreased, later: increased - TM inflamed, poor drainage)
  • psuedo-ptosis
  • CMO
    iris atrophy
    corneal oedema
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7
Q

AAU underlying systemic disease

A

HLA-b27 +ve: Ankylosing spondilitis, Crohn’s disease, Reactive arthritis, Psoriasis
HLA-B27 -ve: sarcoid, TB, Behcet’s disease, Syphilis

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8
Q

Features of ankylosing spondylitis

A
  • Chronic spinal joint disease
    Ache/ stiffness, back ache, rigid spine
    Morning stiffness, gets better with exercise
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9
Q

Features of reactive arthritis (reiter’s syndrome)

A
  • triad: urethritis, conjunctivitis, sero-neg arthritis

- depending on source: STD: M>F, enteric: M=F

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10
Q

Features of psoriatic arthritis

A
  • hyperproliferation of epidermis
  • Small % of psoriasis px develop arthritis
  • 7% arthritic group develop AAU
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11
Q

Features of inflammatory bowel disease

A
  • Colitic arthritis = affects joints, skin
  • Crohn’s disease = bowel inflammation (SI)
  • Ulcerative colitis = inflammation of colon
  • Symptoms: pain, diarrhoea, weight loss, bloody stool
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12
Q

Features of Behcet’s disease (Adamantiades’ disease)

A

Idiopathic
young males
mouth ulcers, genital ulcers, uveitis (post and ant)
Anterior iridocyclitis (hypopyon, keratitis, vitritis, episcleritis, conjunctivitis)
Posterior - diffuse vascular leakage, retinal vasculitis, retinitis

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13
Q

Syphillis

A
  • More common in posterior uveitis

- mx: antibiotics, iv penicillin G (4 units every 4 hours)

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14
Q

Signs of chronic anterior uveitis (CAU)

A
- mild hyperaemia 
normal pupil 
KP
iris nodules 
iris atrophy
secondary cataract
band keratopathy 
CMO
IOP (high- glaucoma, low - hypotony)
Phthisis bulbi (shrivelled eye) 
Rubeosis and fibrovascular membrane
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15
Q

Systemic disease associated with CAU

A
Juvenille idiopathic arthritis (JIA)
Syphilis 
Fuch's uveitis syndrome/ Fuch's heterochromatic iridocyclitis 
Sarcoidosis 
Herpes Zoster Ophthalmicus 
TB
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16
Q

Features of juvenille idiopathic arthritis (JIA)

A
bilateral, non-granulomatous, <16yrs onset, chronic 
- 85% female 
- cells (vitreous/AC)
KP - med/small 
post. synechiae 
CMO
band keratopathy 
examine: 6 weeks of JIA dx --> 2 monthly for 6 months --> 4 monthly until 11yo
17
Q

Features of Fuch’s uveitis syndrome

A

Fuchs dystrophy = corneal endo cell death –> corneal oedema
- Unilateral, insidious onset, non-granulomatous, no hyperaemia, no post. synechiae, no CMO
- Cells and flare
KP - small, grey, stellate
VA declines later

18
Q

Features of sarcoidosis

A
  • multi-systemic inflammation
    Granulomatous, idiopathic
    involves: lungs, lymph nodes, skin, liver, eyes
    Ocular sarcoid (60% have uveitis)
  • large mutton fat KP, iris nodules, bilateral, cataract, glaucoma, phthisis risk
19
Q

Features of Herpes zoster ophthalmicus

A

iris atrophy
cornea (dendritic keratitis, stromal & exposure keratitis), large KP
Glaucoma (high IOP), phythsis
mx: topical antiviral, topical steroid, cycloplegia, glaucoma, oral acyclovir

20
Q

Features of TB

A

most likely CAU, AAU possible

HIV/aids

21
Q

Posner-Schlossman syndrome/ Glaucomato-cyclitic crisis features

A
- v high IOP w open angle during attack 
unilateral, recurrent non-granulomatous trabeculitis 
30-60yrs 
self-limiting, few KPs
55% develop OAG with age