Rheumatology Flashcards

1
Q

Difference between ESR and CRP

A

a. ESR: nonspecific indicator of inflammation

b. CRP: acute-phase reactant; levels ↑ w/ inflammation and infxn

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2
Q

Rheumatic Factor increases in what 5 conditions

A

RA

↑ in Sjogren syndrome,

sarcoidosis,

vasculitis,

chronic infxns

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3
Q

Highest specificity for dx of RA

A

Anti Citrullinated protein antibodies (ACPAs or anti-CCP): higher specificity for dx of RA
+ RF

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4
Q

PE findings of RA ; TXM

A

PE: symmetrical soft, red, tender, swelling in joints (MCP, PIP, sparing DIP)

e. Bilateral ulnar deviation at MCP, boutonniere deformity, swan-neck deformity

TXM = 1st line = METHOTREXATE DMARDs “hydroxychloroquine”

Due to —> Autoimmune Destruction of Joints

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5
Q

Pathophys of OA

A

OA is primarily a disease of cartilage

Presumably in response to this loss, chondrocytes initially proliferate and synthesize enhanced amounts of proteoglycan and collagen molecules.

As the disease progresses, however, reparative attempts are outmatched by progressive cartilage degradation.

Due to —> Wear and Tear on Joints

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6
Q

RF for SLE

A

RF: early age at menarche, OCP use, postmenopausal hormone use, family hx, smoking

Drug induced causes: Hydralazine, INH, Procainamide, Phenytoin, Sulfonamides

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7
Q

PE and Dz of SLE

A

PE: malar rash (“butterfly” rash) , discoid rash, photosensitivity, oral ulces, arthritis, serositis, renal dz, neurologic dz, hematologic d/o, immunologic abnormalities

Dx: + ANA, anti-dsDNA, anti-Smith antibodies, anti-histone antibodies

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8
Q

TXM and goals SLE

A

h. Tx
i. NSAIDs ii. Steroids: mainstay and first line for most lupus manifestations → low dose prednisone daily
iii. Biologic therapies: Belimumab iv. Hydroxychloroquine: ↓ number of dz flares

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9
Q

Scleroderma =

A

Scleroderma (systemic sclerosis): systemic autoimmune dz characterized by varying degrees of skin fibrosis, vascular damage, and organ dysfxn

a. S/Sx: fatigue, stiff joints, pain b. Pt may have tight skin on fingers, facial skin, elbows, knees etc.

Limited or Diffuse

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10
Q

CREST syndrome and assoc w?

A

CREST syndrome:

calcinosis of skin,

Raynaud’s phenomenon,

esophageal dysmotility,

sclerodactyly,

telangiectasia

ASSOC = Scleroderma

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11
Q

Dx labs for scleroderma

A

Dx: anti-Scl 70, anti-centromere antibody (specific for limited dz)

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12
Q

Scleroderma TXM

A

Tx
i. Cyclophosphamide

ii. Tocilizumab and Nintedanib for ILD and IPF

iii. Nifedipine (CCB) for Raynaud’s

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13
Q

S/Sx: low back pain that is worse in morning and improves w/ exercise c. Dx
i. XR shows multiple vertebral fusions (bamboo spine) ii. ↑ ESR

Think? TXM?

A

Ankylosing spondylitis

Tx
i. NSAIDs

ii. PT

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14
Q

Reiters syndrome often has a preceding what infxn?

A

GI or Chlamydia

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15
Q

Reiters Sxs / Dx / TXM

A

b. S/Sx: asymmetric arthritis; conjunctivitis, arthritis, uveitis

c. Dx: + HLA-B27

d. Tx: NSAIDs

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16
Q

Describe acute gouty arthritis

A

Acute gouty arthritis
1. S/Sx: pain and swelling, usually of single joint

  1. MC joints: great toe MTP joint (podagra), ankle, knee, and wrist
  2. Episodes often occur at night
  3. Severe pain
17
Q

Gout Dx

A

Dx: polarized microscopy of synovial fluid showing bright, negatively birefringent, needle-shaped crystals

18
Q

Discuss urate lowering therapy and px txm

A

a. Colchicine 0.6mg daily

b. Low-dose NSAIDs

c. Xanthine oxidase inhibitors: reduce uric acid production
i. Allopurinol ii. Febuxstat

d. Uricosurics
i. Probenecid: enhance urinary excretion of uric acid

e. Biologic therapy
i. Pegloticase

19
Q

Acute gout flares TXM

A

a. NSAIDs (indomethacin, naproxen, ibuprofen, sulindac)

b. Colchicine

c. Glucocorticoids

20
Q

Describe pseudo gout / Dx / TXM

A

b. Pseudogout
i. Caused by calcium pyrophosphate crystals

ii. MC affects knee joint

iii. Dx: joint aspiration shows rhomboid-shaped, weakly positive birefringent crystals iv. Tx: NSAIDs

21
Q

PE of myositis ; Get what?

A

e. PE
i. Malar rash ii. Heliotrope rash: purple rash on or around eyelids
iii. Gottron’s papules: erythematous or violaceous atrophic macules and plaques overlying dorsal
interphalangeal joints of hands

Get = CK (elevated)

22
Q

Myositis TXM

A

Tx
i. Glucocorticoids

ii. Azathioprine

iii. Methotrexate

23
Q

sxs and PE of Fibromyalgia

A
  1. Fibromyalgia syndrome
    a. S/Sx: widespread MSK pain for > 3 mo, nonrestorative sleep, and generalized fatigue

b. PE: tenderness to at least 9 out of 18 anatomic sites (trigger points)

24
Q

TXM Fibromyalgia

A

Tx
i. Education

ii. Antidepressants

iii. Avoid opioids

25
Q

i. S/Sx: monocular visual loss, unilateral HA, jaw claudication

ii. PE: tender, tortuous temporal artery

iii. Dx: ESR > 50

Think? TXM

A

GCA

TXM = High-dose steroids ASAP

Dx = Bx of temporal artery

26
Q

S/Sx: asx pulses or BP, HA, arm claudication, visual changes, arthralgia
Anterior Lead STE’s

A

Takayasu’s Arteritis

27
Q

S/Sx: HTN, glomerulonephritis, abd pain, testicular pain, mononeuropathy (wrist or foot drop)

A

Polyarteritis nodosa (PAN): rare, necrotizing inflammatory vasculitis

28
Q

Buerger’s disease (thromboangiitis obliterans): inflammatory vascular dz

A

Strongly assoc. w/ tobacco products iii. Dx
1. < 50 y/o

  1. Current or recent hx of tobacco use
  2. Distal extremity ischemia
  3. Typical arteriographic findings of TAO
  4. Exclusion of autoimmune dz, thrombophilia, DM, and proximal embolic sources
29
Q

Eosinophilic granulomatosis (Churg-Strauss)
Assoc with?
Sxs?

A

Assoc. w/ severe asthma and systemic eosinophilia

S/Sx: peripheral neuropathy, mononeuritis, and pulmonary and cutaneous involvement

30
Q

Abnml proteins in blood clump together at temperatures < 37C

S/Sx: arthralgia, purpura, skin ulcers, glomerulonephritis, peripheral neuropathy, clonal hematologic dz

Think? TXM?

A

Cryoglobulinemia

Tx
i. Rituximab

ii. Plasma exchange to prevent IgM flare

31
Q

Diseases assoc. w/ HLA-B27

A

PAIR:
psoriatic arthritis,

ankylosing spondylitis,

IBD,

reactive arthritis