Lecture 129 Flashcards

1
Q

MCTD is defined by

A

patients exhibit clinical findings that overlap more than one connective tissue disease

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2
Q

What serological finding is found in most MCTD patients?

A

ANA positive

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3
Q

Clinical criteria for MCTD

A
  1. Swollen hands or fingers
  2. Synovitis
  3. Myositis
  4. Raynaud’s
  5. Acrosclerosis
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4
Q

What is the peak age range for polymyositis/dermatomyositis?

A

40-60 years of age

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5
Q

What region of the body is typically spared in polymyositis?

A

No facial muslce involvement

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6
Q

Classic presentation of polymyositis

A

Bilateral proximal muscle weakness (legs before upper extremities)

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7
Q

Patients with polymyositis can have ____ due to involvement of striated muscles in the ____

A

dysphagia, esophagus

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8
Q

What is the characteristic feature of dermatomyositis?

A

Heliotrope malar rash (dark red)

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9
Q

Where is erythema often present in patients with dermatomyositis?

A

Face, shoulders, upper chest, and back

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10
Q

Gottron papules are seen in what condition?

What do they look like?

A

Dermatomyositis

Red/purple papules over knuckles and extensor surfaces

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11
Q

Patients with dermatomyositis are at a higher risk for ____

A

Malignancy

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12
Q

What syndrome involves a subset of patients with both polymyositis and dermatomyositis, plus SLE-like arthritis?

A

Antisynthetase syndrome

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13
Q

What condition displays anti-Jo-1 autoantibodies?

A

Antisynthetase syndrome (PM/DM)

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14
Q

What condition are anti-Mi-2 autoantibodies specific for?

A

Dermatomyositis

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15
Q

What condition are anti-SRP autoantibodies associated with?

A

Polymyositis

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16
Q

Anti-115/140 autoantibodies indicate an increased risk for:

A

malignancy associated myositis

17
Q

What serological criteria is used to diagnose MCTD?

A

High-titer anti-RNP

18
Q

What is the key difference between MCTD and overlap syndromes?

A

Overlap syndromes do not have anti-RNP antibodies

19
Q

Recurrent oral and genital ulcers plus uveitis is a classic presentation of:

A

Behcet’s disease

20
Q

Behcet’s disease is most common in indivudals from ____

A

the Middle East and Asia

21
Q

What HLA is associated with Behcet’s disease?

A

HLA-B51/B5

22
Q

What treatment is used for severe or refractory Behcet’s disease?

A

TNF-alpha antagonists

23
Q

Pharmacological agents used for Behcet’s disease:

A

Corticosteroids, colchicine, immunosuppressants

24
Q

Fibromyalgia requires widespread MSK pain across ____ or more regions of the body

25
How long must symptoms be present for a fibromyalgia diagnosis?
3 or more months
26
First-line treatments for fibromyalgia
Tricyclic antidepressants/SSRIs/SNRIs