Rheumatology Flashcards

Revise Important Concepts and Information for Rheumatology Year III MBBS Monash University.

1
Q

What are the 5 causes of symmetrical deformity polyarthropathy of the hands?

A
  1. Gout
  2. OA
  3. ## Psoriatic arthritisAutoimmune:
  4. Lupus (SLE)
  5. RA
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2
Q

What are the 5 signs of active synovitis in the hand?

A
  1. Joint line tenderness
  2. Ulnar styloid tenderness
  3. Stress tenderness
  4. Effusion
  5. Bogginess
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3
Q

What are the key findings in X-Ray of a hand of a person with RA?

A
  1. EROSION
  2. DIP is spared
  3. Joint space narrowing
  4. Peri-articular osteopaenia
  5. Concentric
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4
Q

4 Main findings in an X-Ray of a hand of a pt. with OA?

A
  1. Joint space narrowing
  2. Osteophyte
  3. Subchondral sclerosis
  4. Cysts
  5. DIP Not spared
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5
Q

A pt came with widespread joint pain. What do ask in Hx taking?

A
  1. STIFFNESS
  2. Swelling
  3. Worse in the morning/evening? For how long?
  4. Is it better or worse with movement?
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6
Q

If a pt. came with widespread joint pain, after taking Hx, what Ix would you order?

A
  1. FBE: ?anaemia, ?CRP
  2. autoantibodies: ANA. anti-CCP, RhF
  3. U & E, serum uric acid
  4. ESR & CRP
  5. Plain XR: ?OA, ?Psoriatic arthritis
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7
Q

What test is considered ‘the gateway for detecting autoimmune disease’?

What are the percentages of +ve in each one of these:

a. SLE
b. Systemic sclerosis
c. Autoimmune hepatitis
d. RA
e. Sjogren’s syndrome
f. Normal person

A

Anti-nuclear antibody (ANA): +ve by immunofluorescence in:

a. SLE: >95%
b. Systemic sclerosis: 64%
c. Autoimmune hepatitis: 75%
d. RA: 30%
e. Sjogren’s syndrome: 68%
f. Normal person: 0 -2%

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8
Q

In ANA, what pattern of staining is consistent with:

a. SLE
b. mixed connective tissue disease
c. Systemic sclerosis
d. Limited systemic sclerosis

A

a. Homogenous
b. Speckled
c. Nucleolar
d. Centromere

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9
Q

What is the specific test:

a. to detect RA?

b. to detect conn. tissue diseases?
PM
DM
SLE
RA
Systemic sclerosis
Sjogren's syndrome
A

a. anti-cyclic citrullinated peptide Ab (anti-CCP, ~96% specificity)

b.
PM & DM - anti-Jo-1 (esp. for PM) & anti Mi-2

SLE 
dsDNA (~60% sensitivity, highly specific)
anti-La (15%)
anti-SM ( 20-30%)
anti RNP

RA: RhF

Systemic sclerosis: anti-Scl70

Sjogren’s syndrome:???

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10
Q

What does each of this test for?

a. anti-dsDNA
b. anti Jo-1
c. anti Ro
d. anti La (SSB)
e. anti scl70
f. anti-SM

A

a. anti-dsDNA: SLE
b. anti Jo-1: Polymyocitis
c. anti Ro: SLE, Sjogren’s syndrome, systemic sclerosis
d. anti La (SSB): Sjogren’s syndrome [SLE - 15%]
e. anti scl70: diffuse systemic sclerosis
f. anti-SM: SLE; need to check for vasculitis, p-ANCA (?microscopic polymyositis)

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11
Q

What blood test would you do to confirm polymyocitis?

A

anti Jo-1; possibly CK

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12
Q

In a lupus-suspected patient, what questions would you ask? Name four.

A

The American College of Rheumatology: from 11 Diagnostic Criteria

  1. Malar rash
  2. Photosensitivity
  3. Discoid rash
  4. Reynaud’s phenomenon (white, blue, red)
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13
Q

What are the organs commonly affected in SLE?

A

Everything! e.g. mouth, skin joints, brain, kidney, heart.

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14
Q

What are the 11 diagnostic criteria to diagnose SLE?

A
  1. Malar rash
  2. Discoid rash
  3. Serositis: pleurisy or pericarditis
  4. Oral ulcers
  5. Arthritis
  6. Photosensitivity
  7. Blood - haem. disorder
  8. Renal disorder
  9. ANA +ve
  10. +ve ds-DNA
  11. Neurological disorder: seizure, psychosis
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15
Q

The presence of anti Jo-1 autoantibodies is most specific for:

a) polymyositis
b) ankylosing spondylitis
c) SLE
d) CREST Syndrome
e) Sjogren’s syndrome

A

a) Polymyositis

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16
Q

What is the gold standard Ix of osteoporosis?

What is the T-score for osteoporosis Dx?

A

Gold standard: DEXA Bone scan
T- score: 0: better than reference
0 to -1: BMD - Top 84% (no osteoporosis evidence)
-1 to -2.5: Osteopenia
< -2.5: osteoporosis (repeat DEXA in 2 years)

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17
Q

In osteoporosis screening, what is/are the test(s) that should be included in Ix?

A
  1. Vit. D
  2. Ca2+
  3. PTH
  4. Thyroid f(x)
  5. ESR, CRP
  6. U & E (?renal failure)
18
Q

What are the four classes of drugs used to treat osteoporosis?

A
  1. Biphosphonate [1st line: alendronate]
  2. SERM [raloxifene]
  3. strontium renalated
  4. Recomb. PTH/ HRT] e.g. Teriparatide
19
Q

Amy is a 66 years old female, with a Hx of osteoporosis, fracture, and thrombosis (DVT) complicated by pumnonary embolism.

Which of the following drugs is best used in her case?

a) PTH
b) HRT
c) Biphosphonate
d) SERM
e) Strontium

A

b) Hormone replacement therapy (HRT)

20
Q

What are the patterns of joints involvement in gout?

A

All!

Monoarthropathy (Podagra)
Oligoarthropathy
Polyarthropathy

21
Q

Amary is 18 years old, female, with swollen right knee.

Based on your differentials, which Ix would you do?

A
  • Always remember that we need to exclude septic artritis!
    • as age is 18 y/o, unlikely OA, RA, etc.
  1. Fine needle aspiration (need to exclude septic arthritis!)
  2. CRP, ESR
  3. FBE

Extra: if suspect septic arthritis, give fluclox or vancomycin.

22
Q

What are the 5 indications to lower uric acid (a.k.a to undergo uric acid lowering therapy)

A
  1. Multiple episodes of acute gout attack/year
  2. Tophi (or chronic arthritis on exam)
  3. Nephropathy (e.g. kidney/renal stones)
  4. Polyarticualr gout
  5. Extremely high levels of serum uric acid (>12 mg/dl), constantly.
23
Q

What are the drugs used to treat the Sx of gout?

A
  1. NSAIDs (strong): diclofenac 5mg tid
  2. if CI (e.g. peptic ulcer), use colchicine 0.5mg qid
  3. Steroid: to be used if patient has renal impairment.
24
Q

What does these means (on prescription)?

b.i.d
q.d.
t.i.d
q.i.d
q_h

A

b. i.d - bis in die (latin): 2x/day
q. d. - quaque die (latin): 1x/day
t. i.d - ter in die (latin): 3x/day
q. i.d - quarter in die (latin): 4x/day

q_h - q= quaque. h = hours
e.g. 2 caps q4h = 2 capsules every 4 hours

25
Q

What are the drugs used to lower uric acid?

A
  1. Allupurinol
  2. Probenacid (not to be used in acute setting, no effect)
  3. Febuxostate - new kid on the block
26
Q

What are the extra-articular manifest of ankylosing spondylitis?

A
  1. enthesis
  2. acute iritis
  3. aortic regurgitation
27
Q

In ankylosing spondylitis, what is.are the blood test(s) that can be done?

What will be the expected result(s)?

A
  1. FBE (normocytic anaemia)
  2. Increased ESR
  3. Increased CRP
  4. +ve HLA B27
28
Q

Name 6 systemic Comx of steroids.

A
acute:
Acute:
PVD
Psychosis
hyperglycaemia
insomnia
HTN
Skin changes
myopathy
"rebound" inflammation

acute and chronic: immunosuppression (poor wound healing)

Chronic:
Cushing’s syndrome
Osteoporosis
[Diatebes]

29
Q

Mr. A is currently on methotrexate. Name 3 tests you could order to monitor this drug.

A
  1. FBE
    - ?bone marrow over suppression
  2. LFTs
    - can irritate liver (methotrexate SE)
  3. U&E {& GFR):
    - check for methotrexate build up in body fluid {mathotrexate does NOT affect kidney!}
30
Q

How dies inflammation causes osteoporosis?

A

In all inflammation (chronic) –activates–> increase in cytokines (IL-1, IL-6, etc.) - very important link! –activates–> RANK ligand –activates–> oeteoclast (bone eater) –activates–> systemic osteoporosis

31
Q

What are the contraindications of HRT?

A

Divide into 1. CVD, 2. DVT & PE, 3. Malignancy

  1. CVD:
    - cerebrovascular disease
    - Previous: stroke, PVD, AMI
  2. DVT & PE:
    - RF: FHX, T2DM, HTN, Clotting Hx
  3. Malignancy:
    - uterine + cervical cancer
32
Q

Pain
Weakness
Stiffness
Tenderness

a) Match
i) polymyalgia,
ii) polymyositis rheumatica
iii) fibromyalgia, to above description.

b) What abnormality will the blood test shows in each of this condition?

A

1) PMR: STIFFNESS, increased ESR and CRP.
2) PMC: WEAKNESS, increased CK
3) FML: TENDERNESS & PAIN, all normal blood test

33
Q

What are the three drugs used to control gout Sx (a.k.a. acute gout)?

A
  1. NSAIDs (diclofenac)
  2. Colchicine
  3. Steroids
34
Q

Where do gout usually affect?

In a pt. with gout, what does the polarised light microscopy of synovial fluid show?

A
  1. Joints, kidneys, skin

2. Negative birefringence urate crystals.

35
Q

What does +ve p-ANCA and c-ANCA means?

A

p-ANCA: microscopic polyangiitis

c-ANCA: Wegener’s granulomatosis

36
Q

What test is to be done to confirm the Dx of Lupus?

37
Q

Anti-centromere Ab - what does the +ve finding means?

A

Limited systemic sclerosis

38
Q

What is the CREST Syndrome?

A
C - calcinosis (subcut. tissue)
R - Reyanud's
E - Oesophageal + gut dysmotility
S - Sclerodactyly 
T - Telangiactasia
39
Q

In what condition is the CREST Syndrome found?

A

Limited systemic sclerosis

40
Q

What I can be done to confirm limited systemic sclerosis?

A

anti-centromere Ab.