Rheumatology Flashcards

1
Q

Sxs of SLE

A

Symmetric polyarthritis
Pleuritic chest pain
Malar rash
Raynauds

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2
Q

ACR criteria to diagnose SLE

A
Malar rash
Photosensitvity
Polyarthritis
Renal disorders (proteinuria, casts)
Heme disorders (anemia etc)
Anti-DNA, Anti-sm, anti-phospholipid ab
Discoid rash
Mucosal ulcers
Serositis (pleuritis or pericarditis)
Neuro sxs
\+ ANA
(usually need 4+)
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3
Q

General labs used in SLE

A
CBC
Creatinine
U/A
LFTs
ESR/CRP
C3 and C4
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4
Q

What do low complement levels indicate with SLE?

A

Active lupus

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5
Q

Cardinal feature of SLE

A

ANA (but not specific)

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6
Q

How is ANA reported?

A
Titer of antibodies with serial dilution (1:40)
Staining pattern (homogenous, speckled, nucleolar or centromere-loosely associated with underlying autoimmune disease)
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7
Q

Some other things to think about with +ANA

A

RA
Malignancy
Thyroid Probs

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8
Q

ANA subtypes

A

Anti-dsDNA
Anti-Sm
Anti-phospholipid
Only do these if index of suspicion is higher for the diagnosis

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9
Q

What is the anti-dsDNA antibody?

A

Useful to distinguish SLE cause it is rarely seen in other disorders
Often fluctuates with disease activity

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10
Q

What is the anti-smith antibody?

A

Detected in only about half of pts with SLE

Generally remains positive in the pts even with remission

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11
Q

Subtypes of antiphospholipid antibodies

A

Anticardiolipin Ab, beta 2 glycoprotein, lupus anticoagulant
Present in pts with antiphospholipid syndrome
Primary condition or in setting of underlying disease (SLE)

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12
Q

What medical issues are associated with antiphospholipid syndrome?

A

Arterial or venous thromboembolic events

Recurrent fetal loss

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13
Q

Sxs of rheumatoid arthritis

A

Morning stiffness longer than 30 min (inflammatory)- hands, fingers, knees
Redness and swelling of PIP and MCPs (DIPs spared)
Ulnar deviation at MCPs

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14
Q

What is rheumatoid factor?

A

Moderate specificity for RA
But associated with several autoimmune/rheum and nonrheumatic disease
Should also order anti-CCP with it

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15
Q

Rheumatic diseases associated with RF

A

RA, Sjogrens, Mixed connective tissue disease, SLE, polymyositis

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16
Q

Nonrheumatic diseases associated with RF

A

Bacterial endocarditis, hep B/C, TB, sarcoidosis, malignancy, primary biliary cholangitis

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17
Q

What is anti-CCP?

A

Antibodies to citrullinated peptides (ACPA) used when suspicious for RA–antibodies against them are most commonly used b/c specificity is high

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18
Q

Sxs of Sjogrens

A
Fatigue
Dry mouth and dry eyes (sicca complex)
Cavities
Diffuse joint aches
\+ Schermers
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19
Q

Antibodies in Sjogrens

A

Anti-Ro and Anti-La/SSB

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20
Q

Sxs of polymyalgia rheumatica

A

Aching pain in arms, low back, hips and thighs
Acute onset of morning stiffness and stiff with long car rides
Gel phenomenon
Shoulder ROM decreased
(Proximal aching and stiffness)

21
Q

Characteristic lab finding with PMR

A

Increased ESR and CRP (inflammatory markers)

22
Q

What is PMR associated with?

A

Giant cell temporal arteritis

use low dose corticosteroids for this

23
Q

Sxs of fibromyalgia

A

Myalgias and arthralgias
Mind feels foggy
Always tired
May have multiple tender points

24
Q

What do you expect to see on labs fibromyalgia?

A

All normal (CBC, ANA, RF, CRP, ESR)

25
Sxs of ankylosing spondylitis
Low back pain and progressive stiffness (worse in morning) Better with exercise and worse with rest Hx of plantar fasciitis (enthesitis) Bamboo spine, sacroiliitis
26
What lab test is associated with ankylosing spondylitis?
HLA-B27
27
What might you also see HLA B27 with?
Reactive arthritis, psoriatic arthritis or IBD
28
Sxs of systemic sclerosis
``` CREST Calcinosis Raynauds Esophageal involvement Sclerodactyly (tightening of skin on hands and face) Telangiectasias ```
29
What lab supports the diagnosis for limited systemic sclerosis?
Anticentromere antibodies (also have ANA)
30
Lab associated with diffuse cutaneous systemic sclerosis
Anti-scl-70 antibody/antitopoisomerase I (scleroderma)- 70x worse b/c this one is worse
31
What is diffuse cutaneous systemic sclerosis associated with?
Severe interstitial lung disease
32
Normal joint fluid
Viscous, egg white consistency, acellular | Reduce friction b/w articular cartilage of synovial joints
33
Use of arthrocentesis
When sign of effusion of inflammation in joint - For diagnosis - To relieve pressure - To give meds (glucocorticoid, anesthetic etc)
34
Indications for arthrocentesis
New onset acute monoarthritis Suspected crystal induced arthritis Suspected infection/septic arthritis Inflammatory vs noninflammatory arthritides Unexplained joint, bursa or tendon sheath swelling
35
Common aspiration sites
Shoulder, elbow, hip, knee, wrist, ankle
36
Most feared concerns related to arthrocentesis
Septic joint
37
Concerns of glucocorticoid injection
Tendon rupture Nerve damage Osteonecrosis (rare)
38
What else might happen after arthrocentesis?
Skin atrophy or hypopigmentation
39
Categories of joint effusions
Noninflammatory Inflammatory Septic Hemorrhagic
40
Difference in classification of synoial fluid b/w inflammatory and noninflammatory
Inflammatory is >2000 WBCs | Noninflammatory is <2000
41
What is 100,00 WBC until proven otherwise?
Septic
42
Neutrophils (PMNs) in synovial fluid
<25% is noninflammatory | >75% is septic
43
Diagnostic test for septic arthritis
ID of bacteria in synovial fluid
44
Sxs of gout
Severe onset of pain (maybe big toe)
45
What crystals are in gout?
``` Monosodium urate (MSU) Negatively birefringent and needle shaped ```
46
Sxs of pseudogout
See pain in knww etc | Chondrocalcinosis on xray
47
What crystals are in pseudogout?
Calcium pyrophosphate dihydrate (CPPD) | Positively birefringent, rhomboid shape
48
What is birefringent
Material's ability to refract light rays