Infection induced systemic illness characterised primarily by an inflammatory synovitis from which viable microorganisms cannot be cultured
Aetiology
- Most common preceding infections are urogenital (e.g. chlamydia, neisseria) and enterogenic (e.g. salmonella, campylobacter)
Pathophysiology
- Occurs in response to an infection in another part of the body
- Large joints e.g. the knee become inflamed around 1‐3 weeks following the infection
- The infection triggers an autoimmune arthropathy
Clinical presentation
Symptoms
- Present 1-4 weeks after infection
- General symptoms - fever, fatigue, malaise
- Asymmetrical monoarthritis or oligoarthritis
Signs
- Mucocutaneous lesions
- Keratodema blenorrhagica
- Circinate balanitis
- Painless oral ulcers
- Hyperkeratotic nails
- Ocular lesions (uni or bilateral) - conjuntivitis, iritis
- Vissceral manifestations - mild renal disease, carditis
- Reiter's syndrome: triad of urethritis, conjuctivitis/uveitis/iritis and arthritis
Investigations
- Bloods - ↑ inflammatory markers, FBC, U+Es, LFTs, HLA B27 (rarely necessary)
- Cultures - blood, urine, stool
- Joint fluid analysis - rule out infection (aspirate should be negative)
Management
- Treatment is aimed at the underlying infectious cause and symptomatic relief, including IA or IM steroid injections
- Most cases self-limiting - 90% resolve spontaneously within 6 months
- Remaining 10% - chronic progressive erosive disease, requiring DMARDs