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RA Flashcards

1
Q

Three stages of synovial membrane in RA?

A
  1. Exudative phase
  2. Infiltrative phase
  3. Synovial stage
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2
Q

Exudative stage of synovial membrane?

A

acute synovitis (congestion and edema of the synovial membrane) + capillary proliferation and permeability (exudate in joint).

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3
Q

Infiltrative phase/stage of synovial membrane?

A

accumulation of RBC (phagocytosed of these cells  deposition of hemosiderin), PMN, leukocytes, small lymphocytes (predominant cell), distinct multinucleated giant cells (not specific for RA), produce small nodular aggregates superficially called Allison-Ghormley nodules

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4
Q

Synovial stage of synovial membrane?

A

synovial cells enlarge and multiply producing papillary-like fronds, can get metaplasia of connective tissue to fibrocartilage, hyaline cartilage, and even bone (not the same as cartilaginous/osseous debris found in later stages of RA)

  • Increased amounts of turbid yellow-green synovial fluid of decreased viscosity is produced -> increased amounts of globulins (A: G ratio N=2:1, becomes 1:1),
  • Capsular distension, soft tissue swelling and hyperemia
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5
Q

4 early radiographic signs of RA?

A
  1. ST swelling
  2. Hyperemia (periarticular osteoporosis)
  3. Bilat symmetric narrowing
  4. Marginal erosions
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6
Q

RA of the robust reaction type?

A

develop large radiolucent cystic areas in RA patients who maintain high level of physical activity -> physical stress which elevates intra-articular pressure increases rate at which synovial fluid and or pannus is forced into the bone

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7
Q
  • Mechanisms of joint decompression?
A

(1) Formation of synovial cysts
(2) Formation of subchondral cysts
(3) Fistulae/sinus tracts between articulation and skin

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8
Q

sinus tract/fistulous rheumatism mechanism?

A

necrotic bone fragments occurring in rheumatoid joints, if numerous and large, may be extruded through the skin.

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9
Q

Bursal involvement in RA

A
  • Involved because they have a synovial lining, bursa usually communicate with joint which allows spread
  • 5% get bursal involvement, M/C in popliteal region and olecranon, also subacromial (subdeltoid), retrocalcaneal, and in wrist and foot
    posterosuperior calcaneus, olecranon, inferior surface of acromion and distal clavicle, outer aspect of distal ulna from extensor carpi ulnaris tenosynovitis
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10
Q

Cause of edema in RA?

A

causative factors include anemia, fluid retention, hypoalbuniemia, venous or lymphatic obstruction, increased capillary permeability

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11
Q

calcification in RA?

A

– rare, consider overlap with mixed CT disorder or collagen vascular syndromes

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12
Q

Diagnostic Criteria for RA? (7)

A

(1) Morning stiffness in/around joints lasting at least 1 hr before maximum improvement.
(2) Soft tissue swelling (arthritis) of 3+ joint areas observed by physician
(3) Swelling (arthritis) of PIP, MCP, or wrist joints
(4) Symmetric arthritis
(5) Rheumatoid nodules
(6) RF +ve
(7) Radiographic evidence of erosions &/or periarticular osteopenia in hands &/or wrists

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13
Q

Diagnostic criteria must be present how long?

A

Classic RA: >7 criteria with swelling > 6 months
definite = >5 criteria with continuous joint Sx >6 wks
probable = >3 criteria with joint Sx 4-6 wks
probable = at least 2 criteria with joint Sx at least 3 wks

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14
Q

Clinical presentation of RA? (age, sex, sx, etc)

A
  • 2-3x M/C female, 25-55 yoa, onset typically insidious but may follow physical or psychic stress
  • Prodromal Signs – fatigue, anorexia, weight loss, malaise, muscle pain and stiffness
  • Acute arthritic attacks are sudden onset, persist for hrs-days, subside without residual disability
  • A paralyzed limb will notably not develop rheumatoid arthritis.
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15
Q

RA is typically symmetric, when is this not true?

A

symmetry may be absent early in disease as 5-20% have monoarthritis which can last several months
asymmetric or unilateral in pts with neuro deficit, where RA is contralateral to side of paralysis
(RA may be more severe in dominant hand and overused joints)
symmetry is less common in males

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16
Q

Neuropathies in RA?

A

encephalopathy, myelopathy (do to vasculitis, vertebral subluxation, rheumatoid nodules), peripheral neuropathy (stocking distribution of sensory impairment, wrist and foot drop)

17
Q

Felty’s syndrome?

A

RA, splenomegaly, leukopenia, weight loss, anemia, lymphadenopathy, chronic leg ulceration, abnormal skin pigmentation, recurrent infections, M/C female.

18
Q

Sjogren’s syndrome in RA?

A

keratoconjunctivitis sicca, xerostomia (dry mouth), connective tissue disease (60-70% of pts, may be identical to RA)

19
Q

Caplans syndrome?

A

combination of pneumoconiosis and rheumatoid arthritis

20
Q

Other conditions that are RF+?

A

syphillis and SLE.

21
Q

RA Labs?

A
  • Moderate normo/hypochromic anemia, elevated ESR and parallels disease activity, elevated C-reactive protein in active disease state, RF (sheep agglutination test for group of macroglobulins), LE phenomenon (8-27%)
22
Q

Term for multiple marginal erosions seen throughout the carpals

A

spotty carpal sign

Also seen in: gout, tuberculous arthritis and sudecks atrophy

23
Q

Term for radial rotation of proximal row of carpals (70%), and ulnar deviation of MCP joints?

A

zig-zag deformity

24
Q

What is - Caput ulnae syndrome ?

A

pain, limited motion, dorsal prominence of distal ulna do to diastasis at the radioulnar joint with possible dorsal displacement of the ulna causing extensor tendon rupture.

25
Q

% of RA patients with forefoot involvement?

A
  • 80-90% of RA pts, initial manifestation in 10-20%, M/C MTP joints of lateral digits
    Morton’s metatarsalgia due to intermetatarsal bursitis
26
Q

Pattern of hip involvement in RA?

A

soft tissue swelling over greater trochanter (15%)
– concentric loss of joint space with axial migration of femoral head, may result in protrusio acetabuli (15%, a.k.a. Otto’s pelvis, RA is M/C/C of bilateral protrusio), subchondral cysts, osseous collapse of acetabular roof and femoral head, osteoporosis, erosions (begin near femoral neck), sclerosis and osteophytes (overlying DJD?)

27
Q

% of pt’s with C/S involvement?

A

60-80%

28
Q

C/S changes in RA?

A
  • Vertical C1/2 subluxation/cranial settling/atlantoaxial impaction/basilar invagination (may reduce neck length up to 50% called summation effect)
  • Lateral subluxation – lateral masses of atlas displaced >2mm on the axis
  • Subaxial subluxation and dislocation – 9%, M/C C3/4 and C4/5, multilevel subluxations produce a doorstep/stepladder appearance, usually anterior subluxation
29
Q

Septic arthritis and RA?

A
  • Up to 12% of RA pts have suppurative arthritis, up to 50% of pts with suppurative arthritis have RA (MC predisposing factor?)
  • Usually polyarticular, knee is M/C site
  • Infection is M/C/C of death in pts with RA
30
Q

viral etiology of RA?

A
  • Epstein-Barr virus may be precipitating factor by causing formation of the Ag-Ab complexes, enhance RF production, or increase Ab production
31
Q

JRA RF+ %, sex, age?

A
  • 5-10% of children with JCA, M/C females, M/C after 10 yoa
32
Q

JRA RF+ specific findings?

A
  • Periosteal bone formation can involve large segments of the metaphyses of phalanges, metacarpals, and metatarsals. It is the frequency and the severity of periostitis that constitute a fundamental difference between juvenile-onset and adult-onset disease.
33
Q

Stills disease overview?

A
  • Seronegative and no rheumatoid nodules, 70% of JCA, usually <16 yoa
34
Q

Stills - Classic systemic disease?

A

presents under 5 yoa, Represents about 20% of cases of JCA.
associated with severe extra-articular clinical manifestations.
- Onset of acute high remitting fever +/- arthritis, 80-90% have a rash with fever
- can mimic leukemia or lymphoma

35
Q

Stills - Polyarticular disease?

A
  • M/C form of JRA (50%), 2x M/C in females
  • May occur during onset of Still’s disease or later
  • 20% of pts with JCA, poor prognosis
  • Bony ankylosis common in wrist and foot, premature epiphyseal fusion resulting in growth defects
  • Hip involved in 40%, may develop joint abnormalities including protrusio
  • C/S abnormalities may be a presenting feature in 2%, facet erosions and ankylosis, especially upper C/S (C2/3 M/C), hypoplasis of Vertebral Bodies and IVD’s
36
Q

Stills - Pauciarticular/monoarticular disease

A
  • 30-70% of JCA cases, 3x M/C female.
  • Confined to large joints  M/C knees (M/C monoarticular location), ankles, elbows, wrists
  • Monoarticular onset may develop iridocyclitis which may cause blindness
  • Lymphadenopathy, splenomegaly, fever, rash
37
Q

Similar findings between JCA and Hemophilia?

A

osteoporosis, soft tissue swelling, ballooning of distal femoral and proximal tibial epiphyses, flattening of the femoral condyles, widened intercondylar notch, joint space narrowing, erosions, squaring of patella
may develop tibiotalar slant
– radial head may be enlarged

38
Q

JCA facial findings?

A
  • 10-20% micrognathia with bite and TMJ abnormal, bird face (10-30%) do to arrested mandibular growth with normal growth of other facial features

RA (2 decks)

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