Rheumatology Flashcards

1
Q

How are diagnosis made

A

Arthrocentesis and joint fluid analysis

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2
Q

Common sites for joint aspiration

A
Shoulder
Elbow
Wrist
Hip
Knee
Ankle
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3
Q

Characteristics of normal synovial fluid

A

Highly viscous (hyaluronic acid)
Clear
Acellular
Protein and Gluose (not specific)

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4
Q

Categories of joint effusions

A

noninflammatory
inflammatory
septic
hemorrhagic

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5
Q

What are you looking for on joint fluid analysis

A

Gross appearance
Microscopic exam
Gram stain & culture
Presence of crystals

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6
Q

Non inflammatory disease states

A

OA
Traumatic arthritis
Osteonecrosis
Charcot arthropathy

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7
Q

Inflammatory disease states

A

RA
SLE
Poly/Dermatomyositis
Systemic sclerosis

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8
Q

Septic disease states

A

Bacterial

Fungal

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9
Q

Hemorrhagic disease states

A

Traumatic tap
Trauma
Neoplasia
Coagulopathy

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10
Q

WBC

A

Normal

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11
Q

WBC

A

Non-inflammatory

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12
Q

WBC > 100000

A

Septic (until proven otherwise)

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13
Q

50000 - 100000

A

Make sure you rule out sepsis

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14
Q
A

Non inflammatory

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15
Q

Gout

A

Monosodium urate crystals
Negatively birefringent; needle shape
intra/extra cellular

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16
Q

Pseudogout

A

Calcium pyrophosphate
Positive birefringent; rhomboid shape
Intra/extracellular

17
Q

How is birefringence determined

A

Polarized light microscopy

18
Q

What is the gold standard for evaluating crystals

A

Polarized light microscopy

19
Q

What is birefringence

A

Ability to refract light rays (use compensator filters)`

20
Q

What is the down side of Rheumatoid factor

A

Poor specificity (autoimmune, rheumatic and non-rheumatic dz)

21
Q

What does a positive ANA (Anti Nuclear Antibodies) consist of

A

Titer and staining pattern (outline, speckled, homogenous, nucleolar)

22
Q

Diseases w/ positive ANA

A
RA
SLE
Scleroderma
CREST
Poly/Dermamyositis
23
Q

Anti-dsDNA

A

SLE (malar rash)

Titer decreases w/ successful therapy and increases w/ exacerbation or meds

24
Q

Anti-Smith (Anti-Sm)

A

SLE

25
Q

Anti-Ro/SSA, Anti-La/SSB

A

Sjorgen (diagnostic)

Titers decrease as it becomes less active

26
Q

Anti-scleroderma-70 aka Antitopoisomerase I antibody

A
Systemic sclerosis (Scleroderma)
Absence of antibody doesnt rule out scleroderma
27
Q

Anticentromere (ACA)

A

CREST

28
Q

ESR/CRP

A

ESR ≥ 40 (forty) diagnostic fo polymyalgia rheumatica

Elevated ESR; think Giant cell temporal arteritis and cn cause blindness

29
Q

Human Leukocyte Antigen (HLA-b27)

A

Ankylosising spondylitis

Also seen in : Reactive arthritis, psoriatic arthritis, arthritis/spondylitis associated w/ IBD

30
Q

Antiphospholipid antibodies

A

Antiphospholipid syndrome
primary condition or secondary to underlying diseases usu SLE
Female recurrent fetal loss w/ Hx of thrombosis

31
Q

Chronic symmetric polyarthritis, positive RF, +/- anti CCP

A

RA

32
Q

Polyarthritis, rash, nephritis, serositis, +ve ANA, anti-DS DNA +/- anti-Smith

A

SLE

33
Q

Acute onset of proximal myalgia, morning stiffness, >55yo, high ESR, Prompt improvement with low dose corticosteroids

A

Polymyalgia rheumatica

34
Q

Tender points, non-restorative sleep, normal test results

A

Fibromyalgia

35
Q

Sicca complex, anti-Ro/SSA, Anti-La/SSB

A

Sjorgens

36
Q

CREST syndrome, anti SCL-70, ACA

A

Systemic sclerosis (scleroderma)