Rheumatoid arthritis Flashcards

1
Q

What is the pathogenesis for bony erosion in RA?

A

RANKL (in synovial fibroblasts and T-cells) binds RANK on osteoclasts

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2
Q

What is pathogenesis of RA?

A
  • self-reactive CD4+ T-cells produced Th1 and Th17 cytokines—> cascade of inflammation
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3
Q

In RA, ___ and ____ form immune complexes inside joints–>activation of complement

A
  • RF and anti-CCP antibodies
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4
Q

What causes the Majority of cutaneous findings in RA?

A
  • neutrophil-mediated damage (as a result of complement activation)
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5
Q

Gene affected in RA?

A
  • PTPN22
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6
Q

HLA assocation in RA:

A

HLA-DRB1

(patients with RA cant participate in the home run DRB1)

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7
Q

What is the diagnostic criteria for RA called?

A
  • ACR/EULAR (see pg 116 for criteria)
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8
Q

rheumatoid nodules occur more commonly in RA patients with high _____ titers.

A

RF

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9
Q

How do rheumatoid nodules present clinically?

A
  • firm, non-tender papules or nodules over bony prominences
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10
Q

What is rheumatoid nodulosis?

A

this is a variant of RA with:

  • high RF

- multiple ulcerative rheumatoid nodules

-ABSENCE of active joint disease

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11
Q

Who gets therapy-induced rheumatoid nodulosis? How does it present?

A
  • patients w/ preexisting RA following initiation of MTX or TNF-alpha inhibitor therapy
  • Acute onset of numerous symmetrically grouped rheuymatoid nodules that are often PAINFUL (unlike normal rheumatoid nodules which are painless)
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12
Q

Rheumatoid vasculitis management:

A
  • refer to rheum for aggressive therapy (high mortality up to 40%)
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13
Q

In what setting will you see Rheumatoid vasculitis?

A
  • long standing history of erosive RA with high RF titer
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14
Q

What are Bywater’s lesions?

A

Purpuric papules usually on digital pulp seen in RA

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15
Q

If you see numerous atrophic, shiny, telangiectatic, yellow plaques w/ red-brown edges resembling NLD w/ ulceration on the lower extremities in RA patient, this is_____

A

superficial ulcerating necrobiosis (aka rheumatoid necrobiosis)

- occurs in severe RA w/ high RF titer

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16
Q

What neutrophilic dermatoses are seen in RA patients?

A
  • Swets
  • Erythema elevatum diutinum
  • PG
  • MTX-induced papular eruption
  • Palisaded neutrophilic granulomatous dermatitis
  • Interstitial granulomatous dermatitis
17
Q

How does rheumatoid neutrophilic dermatitis present?

A

persistent urticarial red papules/plaques symmetrically distributed on extensor forearms and hands

  • these may represent earliest face of rheumatoid nodules
18
Q

How does interstitial granulomatous dermatitis w/ arthritis present?

A
  • Annular red-violaceous plaques on trunk and intertriginous areas, sometimes with “rope sign” (red-flesh colored cords extending down flanks or back)

- seen in patients with RA (if without arthritis is simply IGD)

19
Q

Histopath of rheumatoid nodules, early and late:

A

early: interstitial granulomatous or neutrophilic infiltrate
late: large palisading granulomas surrounding degenerated eosinophilic connective tissue (“necrobiosis”) and Fibrin

20
Q

Tx for acute flare of RA?

A

steroids (as a bridge to DMARD)

21
Q

First line long term therapy for RA? Second line?

A

MTX (also can use sulfasalzine, hydroxychloroquine, and leflunomide) + NSAIDS

  • second line is biologics (TNF-AI)
22
Q

How to treat rheumatoid nodules?

A
  • can try intralesional CS or excision (recurrence common)

do not respond to treatment of arthritis

23
Q

Prognosis of RA?

A
  • chronic progressive disease activity that waxes and wanes over time
24
Q

Mortality rate compared to general population in RA patients? Most common cause of death in RA?

A
  • two times higher mortality than general population

Ischemic heart disease

25
Q

What is Felty syndrome?

A

RA w/:

- neutropenia

- splenomegaly

- refractory leg ulcers (resembling PG)