pathophys Flashcards

(29 cards)

1
Q

what 5 joints does OA usually effect? gender predilection?

A
  • hands, PIP and DIP, CMC of thumb (women)
  • knees (women)
  • hips (men)
  • feet (MTP 1)
  • spine
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2
Q

what joints does OA secondary to DM neuropathy affect?

A

MTPs 2-5 also

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3
Q

what two genetic alleles predispose to RA?

A

HLA-DRB1

PTPN22

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4
Q

what antibodies are most specific to RA? what other antibodies are associated with RA?

A

anti-CCP

rheumatoid factor

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5
Q

what immune response is implicated in RA?

A

TH1 and TH17

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6
Q

which joints in the hand does RA affect? what joints may it affect that aren’t usually affected in OA?

A

MCP and PIP, not DIP

shoulder and ankle

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7
Q

what is different between the spinal involvement of OA and RA?

A

RA: only cervical spine with risk of spinal cord compression

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8
Q

what confers genetic predisposition to SLE?

A

HLA-DR2
HLA-DR3 weakly
C1q, C2 or C4 complement deficiency

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9
Q

which antibodies are specific to SLE and what are they associated with?

A

anti-dsDNA: nephritis
anti-SM: none
antiphospholipids: clotting, spontaneous abortions

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10
Q

what resembles RA but shows no erosions, deformities are reducible?

A

Jaccoud’s-like arthropathy: arthritis in SLE with history of rheumatic fever

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11
Q

what T cell response is seen in scleroderma?

A

TH2: alternative macrophage activation and collagen deposition

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12
Q

what suggests autoimmune etiology with Raynaud’s?

A

widened capillary loops in nail-bed

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13
Q

what antibodies are associated with diffuse SSc, limited SSc, and scleroderma renal crisis?

A

diffuse SSc: anti-topoisomerase 1 (anti-Scl70)
limited SSc: anti-centromere
renal crisis: anti-RNA polymerase III

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14
Q

what antibody is associated with overlap syndrome (SLE, scleroderma, MCTD)?

A

anti-U1-RNP

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15
Q

what is the most common cause of death in diffuse SSc?

A

interstitial lung disease, PAH

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16
Q

what is the clinical presentation of limited SSc

A
CREST
calcinosis
Raynaud
esophageal dysmotility
sclerodactyly
telangiectasia
17
Q

what disease characteristics are seen in MCTD? what is the most common cause of death?

A

lupus, scleroderma, myositis

PAH

18
Q

what antibodies are somehwat sensitive but not specific to Sjogren’s? which are specific?

A

ANA and rheumatoid factor

anti-Ro (SSA) and -La (SSB)

19
Q

what is the negative predisposition for spondyloarthropathies?

20
Q

how does reactive arthritis present? what is the genetic predisposition?

A

HLA-B27

  1. arthritis
  2. urethritis
  3. conjuncitivitis
21
Q

which specific cytokine is increased in psoriatic arthritis?

22
Q

what disease is anti-Jo-1 antibody associated with?

A

polymyositis and dermatomyositis with arthritis

23
Q

what other organ is infected in 70% of inflammatory myopathies?

A

interstitial lung disease

24
Q

what should be tested for following diagnosis of inflammatory myositis, esp. dermatomyositis?

A

malignancy in 12%

25
what inflammatory cells are implicated in DM vs PM/IBM?
DM: CD4, macros, dendritic cells | PM/IBM: CD8 and macros
26
with arthritis, what differentiates the rashes of dermatomyositis and SLE?
DM rash affects knuckles, SLE spares knuckles and affects phalanges DM doesn't spare nasolabial folds
27
what is cracking hyperkeratosis of skin over fingers with arthritis of those small joints a sign of?
dermatomyositis or polymyositis
28
how can polymyositis be clinically differentiated from inclusion body myositis?
IBM is resistant to glucocorticoid treatment
29
how can inflammatory myopathies and polymyalgia rheumatica be differentiated in lab?
myopathies: increased CPK polymyalgia: elevated ESR