Lupus and other CT disorders Flashcards

1
Q

How many diagnostic criteria do you have meet to classify SLE?

A

4/11 criteria needs to be met

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2
Q

how do you distinguish the butterfly (malar) rash from rosacea?

A

butterfly rash has a nasolabial food

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3
Q

what are some symptoms of lupus?

A
  • butterfly rash
  • alopecia
  • painless mucosal ulceration
  • Jaccoud’s arthropathy
  • CNS involvement
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4
Q

what is the most devastating manifestation of lupus?

A

renal disease- lupus nephritis

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5
Q

what is ANA testing useful for?

A

ANA has high sensitivity (100%) but low specificity

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6
Q

what does (-) ANA tell you?

A

you do not have SLE

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7
Q

what does (+) ANA tell you?

A

many causes for (+)ANA

  • malignancies
  • infections
  • other autoimmune dz
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8
Q

which test is SPECIFIC for SLE?

A

anti ds-DNA

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9
Q

what is significant about (+)anti ds-DNA?

A

often associated with renal involvement (so it has poor prognosis)
-and it waxes and wanes with disease activity

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10
Q

what other marker is quite specific for SLE?

A

anti-Smith

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11
Q

which factors increase risk for avascular necrosis?

A
  • steroid use
  • antiphospholipid antibody positvity
  • hyperlipidemia
  • Raynaud’s phenomenon
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12
Q

what is the hallmark of inflammatory myopathies?

A

painless proximal muscle weakness

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13
Q

do children mostly have dermatomyositis or polymyositis?

A

children- dermatomyositis

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14
Q

in adults, which inflammatory myopathy is more common?

A

polymyositis- most common

dermatomyositis may indicate paraneoiplastic syndrome

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15
Q

what is Gottron’s papules?

A

rash around knucles indicative of dermatomyositis

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16
Q

how many criteria do you need to fill for polymyositis?

A

4 out of 5 criteria

17
Q

how many criteria do yo uneed to fill for dermatoymyositis?

A

3 out of 4 criteria

18
Q

Name the 5 criteria for inflammatory myopathies.

A
  • symmetric proximal muscle weakness
  • elevated muscle enzymes
  • myopathic EMG abnormalities
  • typical changes on muscle biopsy
  • typical rash of dermatomyositis
19
Q

which autoantibody is commonly seen in inflammatory myopathies?

A

anti-Jo1

20
Q

describe the involved skin in limited scleroderma.

A

distal extremities & face are involved (but trunk is spared)

21
Q

what does CREST stand for? CREST is a limited cutaneous system sclerosis.

A
Calcinosis
Raynaud's
Esopheal dysmotility
Sclerodactyly
Telangiectasias
22
Q

describe the color changes seen in Raynaud’s.

A

1st white- vasospasm
2nd blue- cyanosis
3rd red- reperfusion hyperemia

23
Q

which antibody is seen in limited scleroderma?

A

anti-centromere

24
Q

which antibody is seen in diffuse scleroderma?

A

anti-Scl-70

25
Q

describe treatment for scleroderma.

A

treatment is very frustrating-steroid use is limited; only symptomatic treatment

26
Q

what disease must be present for scleroderma?

A

Raynaud’s