4. Arthritis Flashcards

1
Q

Types of arthritis

A
  1. Osteoarthritis
  2. Rheumatoid arthritis
  3. Seronegative arthritis
  4. Crystalline joint disorders
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2
Q

Definition of osteoarthritis

A

Also known as degenerative joint disease; involves progressive erosion of articular cartilage of joints

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3
Q

Causes of osteoarthritis

A

i. Primary osteoarthritis (95% of cases, idiopathic)

ii. Secondary osteoarthritis (5% of cases)
1. Underlying joint disorders
- Previous septic arthritis
- Congenital dislocations
- Inflammatory arthritis
- Intra-articular fracture

  1. Abnormal stresses
    - Malaligned joints
    - Neuropathic joints (lack of sensation)
  2. Metabolic/endocrine causes
    - Gout
    - Hemachromatosis
    - Diabetes mellitus
    - Marked obesity
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4
Q

Site of osteoarthritis

A
  1. Primary arthritis
    - Typically a generalized process
    - Involves distal & proximal interphalangeal joints of the hand (gives Heberden nodes, prominent osteophytes at the DIP, especially in women)
  2. Secondary arthritis
    - Typically a localized process
    - Involves single large joints, typically knee or hip
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5
Q

Morphology of osteoarthritis

A

Grossly:
1. Alteration in shape & damage to articular cartilage

  1. Eburnation
    - Smoothening of surface of subchondral bone plate exposed due to focal areas of complete loss of articular cartilage
  2. Thickening of subchondral bone
  3. Subchondral cyst formation
    - Cystic lesions representing intraosseous accumulation of synovial fluid leaked through gaps in exposed subchondral bone
  4. Osteophyte formation
    - Mushroom-shaped bony outgrowths at the margins of the articular surface
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6
Q

Clinical features of osteoarthritis

A
  1. Presentation:
    - Deep achy pain that worsens with use
    - Morning stiffness, limited range of movement
    - Impingement of osteophytes on spinal foramina (in the case of osteoarthritis of intervertebral joints) may cause nerve root compressions, leading to pain, spasms & muscle atrophy
  2. Xray findings:
    - Narrowing of joint space
    - Increased thickness of subchondral bone
    - Subchondral cyst formation
    - Osteophyte formation (large peripheral growths of bone & cartilage)
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7
Q

Definition of rheumatoid arthritis

A

Chronic systemic inflammatory disease that frequently involves the synovial lining of peripheral joints

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8
Q

Epidemiology & associations with rheumatoid arthritis

A
  1. Male : female= 1 : 3
  2. Often occurs in 4th to 6th decades of life
  3. Complex mode of inheritance under polygenic regulation
    - Class II MHC molecules play an important role
    - Strong association with HLA-DR4
  4. Rheumatoid factor (one of the many autoantibodies produced in rheumatoid arthritis)
    - Not specific for rheumatoid arthritis though
    - Seen in a number of no rheumatic diseases as well as
    in healthy individuals
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9
Q

Pathogenesis of rheumatoid arthritis

A
  1. Inappropriate activation of CD4+ T-helper cells results in the activation of several inflammatory pathways:
    - B cell activation to produce autoantibodies (rheumatoid factor) which results in immune complex deposition in synovial joint
    - Macrophage activation which releases cytokines promoting fibroblast, chondrocytes & synovial cells to release collagenase, stromalysin, elastase etc
    - Endothelial activation which upregulates adhesion molecule expression, promoting the recruitment of leukocytes & subsequent inflammation
  2. These pathways converge upon a pannus formation
    - Pannus = hypertrophied inflamed synovium which extends over the articular surface & destroys the underlying cartilage & bone
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10
Q

Morphology of rheumatoid arthritis

A

Histologically:
1. Synovial hyperplasia

  1. Accumulation of chronic inflammatory cells (plasma cells, lymphocytes, macrophages, giant cells)
  2. Subcutaneous rheumatoid nodules (seen in 25% of cases, irregularly shaped with a central zone of necrotic fibrinoid material surrounded by a palisade of histiocytes & some chronic inflammatory cells)
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11
Q

Clinical features of rheumatoid arthritis

A

Presentation:

  1. Generally symmetrical involvement of joints, progressing from small to large joints
    - Hands & feet first, followed by elbows, knees, wrists, ankles, hips, spine & temporomandibular articulations
    - Swan-neck/boutonniere fingers: characteristic radial deviation of wrist & ulnar deviation of fingers + flexion-hyperextension of fingers (due to damaged tendons, ligaments & joint capsule)
  2. Involved joints are swollen, warm, painful & particularly stiff following inactivity & sleep
  3. Alleviation of symptoms occur with use of joint
  4. Extra-articular multisystemic manifestations:
    - CVS: ischemic heart disease, atherosclerosis, vasculitis
    - Rheumatoid nodules in soft tissue, lungs & viscera
    - Lungs (interstitial lung fibrosis)
    - Serosal inflammation (pericarditis, pleurisy)
    - Microcytic hypochromic anemia
    - Felty’s syndrome (less than 1% of patients develop splenomegaly & leucopenia)
    - Ocular disease (keratoconjunctivitis sicca, scleritis, perforation of the globe)

Treatment:

  1. Methotrexate (first line treatment)
  2. Corticosteroids
  3. NSAIDs
  4. Anti-TNF agents
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12
Q

Definition of seronegative arthritis

A

Group of disease that develop in genetically predisposed individuals, initiated by ubiquitous environmental factors such as infectious agents; typically negative for rheumatoid factor, associated with HLA-B27 & display a predilection for young men

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13
Q

Types of seronegative arthritis

A
  1. Ankylosing spondylitis
  2. Reiter syndrome
  3. Psoriatic arthropathy
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14
Q

Ankylosing spondylitis

A
  1. Aka rheumatoid spondylitis or Marie-Strumpell disease
  2. Chronic synovitis that causes destruction of articular cartilage with resultant bony ankylosis
    - Involves vertebral column & sacroiliac joints of young patients
    - Eventual squaring & fusion of vertebral bodies & production of bony outgrowths result in severe spinal immobility
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15
Q

Complications & associated pathologies of ankylosing spondylitis

A
  1. Spine fracture

2. Aortitis, uveitis, amyloidosis

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16
Q

Reiter syndrome

A
  1. Aka reactive arthritis
  2. Usually follows an episode of venereal disease & other infections:
    - Salmonella, Shigella, Yersinia, Campylobacter, Chlamydia
17
Q

Symptoms of Reiter syndrome

A

Characteristic clinical triad of symptoms:
“cannot see, cannot pee, cannot bend your knees”
1. Conjunctivitis
2. Urethritis
3. Seronegative polyarthritis
- Usually asymmetrical involvement of joints
- Most often affects ankles, knees & feet

18
Q

Complications & associated pathologies of Reiter syndrome

A
  1. Aortic regurgitation

2. Cardiac contraction abnormalities

19
Q

Psoriatic arthropathy

A
  1. Involves 10% of patients with psoriasis
  2. Typically asymmetrical involvement of joints
    - DIP joints of hands, feet, knees, hips, ankles
    - May involve spine & sacroiliac joints
20
Q

Definition of crystalline joint disorders

A

Gout & pseudogout; important to recognize as they may clinically mimic septic arthritis or inflammatory arthritis; investigation modalities include polarized microscopy of joint fluid for crystals (either fresh or in alcohol as crystals dissolve in water based solutions like formalin) & culture + gram stain of joint fluid for organisms

21
Q

Types of crystalline joint disorders

A
  1. Gout

2. Pseudogout

22
Q

Gout

A

Group of diseases characterized by increased uric acid levels with deposition of urate crystals in joints & kidneys

  1. Most cases due to impaired uric acid excretion by kidneys
  2. Sodium urate crystals precipitate from saturated body fluids
  3. Attempted phagocytosis of urate crystals leads to the activation of an inflammatory response
23
Q

Polarized microscopy for gout

A

Classic birefringent needle shaped crystals (negatively birefringent)

24
Q

Complications of gout

A
  1. Gouty tophi (deposition of crystals in joints or soft tissues forming tophus)
  2. Joint deformities & destruction
  3. Kidney disease: uric acid stones, urinary tract obstruction, infection
25
Q

Pseudogout

A

Also known as calcium deposition disease (CPPD)

  1. Involves deposition of calcium pyrophosphate dihydrate in synovial membranes
  2. Idiopathic, associated with trauma
26
Q

Polarized microscopy for pseudogout

A

Weakly birefringent rhomboid shaped crystals (weakly positively birefringent)