Rheumatoid Arthritis Clinical Features

Clinical Features

  • Typically insidious onset
  • Most commonly presents with
    • Morning stiffness
    • Malaise
    • Fatigue
    • Fever
    • Weight loss
    • Symptoms pain & swelling in hands/ wrists/ feet
  • 10% have abrupt onset with systemic signs
    • Fever
    • Chills
    • Rash
    • Adenopathy
    • Splenomegaly
    • Visceral involvement
    • Stills Disease
  • May precede the articular manifestations
  • Hands/ wrists, elbows, shoulders, knees, ankles & neck often involved
  • hip & DIPJ rarely involved
  • Four Presentations
    • Slowly Progressive Polyarthritis
      • Gradually worse over months
      • Involves one then another joint
    • Episodic Polyarthritis
      • Acute swelling of one joint
      • Resolves with asymptomatic interval
      • Intervals shorter until polyarthritis develops
    • Monoarticular or Oligoarticular Arthritis
      • Swollen large joint
      • Polyarthritis develops later
    • Fulminating Polyarthritis
      • More common in elderly
      • Acute onset with widespread joint involvement
      • Marked systemic signs
  • Four Outcomes
    • Short-lived
      • 25%
      • No disability
    • Mild
      • 25%
      • Mild disability
    • Progressive
      • 40%
      • Variable progressive deformity
    • Severe
      • 10%
      • Gross deformity
      • Severe disability
      • Rapid progressive
  • Really 2 subgroups » those that…
    • Do well
    • Do REALLY BADLY
  • Early Features
    • Symptoms
      • Early morning joint stiffness
      • Stiff after rest
      • Joint swelling
        • Especially hands
      • Polyarthralgia
        • Initially fingers
        • Then wrists, feet, knees & GHJ
      • Systemic symptoms
        • Weight loss
        • Fever
        • Malaise
    • Signs
      • Symmetrical joint swelling & pain
        • Especially MCPJ/ PIPJ/ wrist
        • Joint tenderness on deep palpation
        • Limited ROM
      • Tenosynovitis
        • Flexor tendon sheaths of fingers
        • Extensor compartments of wrists
      • Autonomic dysfunction
        • Hyperhidrosis
        • Palmar Erythema
      • Nerve entrapment
        • CTS
      • Telangiectasia
      • Eye involvement

Articular Disease

  • Hands
    • Early see PIPJ swelling from synovitis
    • Bilateral MCPJ symmetrical swelling
    • Fingers ulnar deviate & MCPJ sublux
    • Swan Neck & Boutonierre deformities
    • Z deformity of the thumb
    • Extensor tendon rupture
    • Causes of dropped fingers in rheumatoid include
      • MCPJ subluxation
      • Ulnar subluxation of tendons
      • Extensor rupture
      • PIN palsy
      • Trigger finger
  • Wrists
    • Active extensor synovitis
    • CTS secondary to flexor synovitis
    • DRUJ involvement with Caput Ulnae syndrome
    • Wrist ankylosis & loss of function
  • Elbows
    • FFD common even early
    • Radial head disease & synovitis common problem
    • Can see Ulnar N entrapment
  • Shoulders
    • G-H & the A-C joints involved
    • Rotator cuff disease common
  • Hips
    • Less common, later development
    • May see Protrusio or AVN from steroids
  • Knees
    • One of most commonly affected
    • Synovitis common
    • FFD & valgus angular deformity common (although most are varus deformities)
    • Bakers cyst common
  • Feet & Ankles
    • Subtalar joint more often affected than the ankle joint
    • Subsequent planovalgus deformity seen
    • Posterior tibial & peroneal tendonitis
    • Can see plantar fasciitis or tendo achilles bursitis
    • Mortons Neuroma seen
    • Forefoot disease with
      • Hallux valgus
      • Lateral deviation of the lesser toes
      • Clawing of toes
      • MTPJ subluxation & distal progression of the fat pad
  • Cervical Spine
    • Intermittent neck stiffness & pain common
    • Neurological symptoms rare
    • Atlanto-axial instability & Basilar invagination of the odontoid can be seen
    • Subaxial vertebrae may also demonstrate instability

Extra-Articular Involvement

  • Nodules
    • Occur in 25% of patients
    • Pathognomonic
    • Associated with IgM RF
    • Most commonly occur on subcutaneous surface of forearms
    • Also found in other areas of pressure
      • Around knee
      • Back of skull
      • Bridge of nose with glasses
      • Sacrum
      • Flexor tendons with triggering
      • Pleura & Lung
      • Pericardium & Myocardium
      • Larynx
      • Sclera
    • Differentiate from
      • Gouty tophi
      • BCC
      • Xanthomata
      • Sebaceous cyst
  • Vasculitis
    • Obliterative Endarteritis
      • Digital vessels
      • Nailfold lesions
      • Cutaneous lesions of pulps
Raynaud’s
  • Inflammatory Vasculitis
    • Polyneuritis
    • Skin infarction & ulceration
  • Neuropathy
    • Spares the CNS but PNS often affected
    • Mononeuritis Monoplex
      • Related to vasculitis
    • Symmetrical distal polyneuropathy
      • NOT related to vasculitis
        • Sensory Polyneuropathy
        • OR
        • Motor & Sensory Polyneuropathy
      • More common in Seropositive men with chronic disease
    • Entrapment Neuropathies
      • CTS
      • Ulnar Tunnel Syndrome
      • Cubital Tunnel Syndrome
      • Supinator Syndrome
      • Tarsal Tunnel Syndrome
  • Cervical Myelopathy
    • Cord compression due to Atlantoaxial instability
  • Myopathy
    • Due to
      • Myositis from vasculitis
      • Steroids or Anti-malarial treatment
  • Other manifestations
    • Ocular
      • All present with Red eye
      • Include
        • Episcleritis
        • Keratoconjunctivitis Sicca/ Sjogren’s Syndrome
        • Scleromalacia perforans
      • Gold & Chloroquine treatment can cause ocular side effects
  • Pulmonary
    • Pleural effusions
    • Intrapulmonary rheumatoid nodules
    • Pneumoconiosis » Caplan’s Syndrome
      • Pleurisy
      • Diffuse Interstitial Fibrosis
    • Pulmonary HT from vasculitis
  • Cardiac
    • Pericarditis
    • Nodules causing
      • Valvular insufficiency
      • Conduction defects
  • Lymphadenopathy
    • Nodes draining affected joints
    • Nodes at a distance
    • Due to hyperactivity of RES
  • Anaemia of Chronic Disease
    • Normocytic normochromic
    • Low Serum Iron
    • Worst if iron loss due to NSAID
  • Felty’s Syndrome
    • Chronic RA & splenomegaly/ lymphadenopathy
    • May also see skin pigmentation, leg ulcers, anaemia, thrombocytopaenia
    • Gram positive infections common