Muscle Diseases Flashcards

1
Q

What is the pathophysiology of polymyositis?

A

T cell mediated destruction of muscle

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2
Q

What are the clinical features of polymyositis?

A
Symmetrical muscle weakness in PROXIMAL upper and lower limbs --> difficulty climbing stairs, brushing hair etc
Insidious onset
Dysphagia in 1/3 (poor prognosis)
Interstitial lung disease (5-30%)
Increased risk of malignancy
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3
Q

What are the clinical features of dermatomyositis?

A

Same as polymyositis + cutaneous features:

  • heliotrope rash (around eyes)
  • Gottron’s papules on hands (over knuckles)
  • V-shaped rash over chest, ‘shawl sign’ rash over upper back
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4
Q

Which investigations should be done for poly/dermatomyositis? Which is definitive?

A

Bloods
EMG (abnormal in 90%)
Muscle biopsy –> definitive diagnosis
MRI

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5
Q

Which blood tests should be done for poly/dermatomyositis? What would they show?

A

Inflammatory markers –> raised
CK –> raised
Autoantibodies:
- anti-Jo-1, anti-SRP –> specific for myositis
- ANA, anti-RNP –> seen in other conditions

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6
Q

What would be seen on muscle biopsy in myositis?

A

Perivascular inflammation + muscle necrosis

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7
Q

What is the management of myositis?

A
Corticosteroids --> prednisolone
Immunosuppression:
- azathioprine 
- methotrexate
- ciclosporin
- IV Ig
- rituximab
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8
Q

Patients with myositis are at an increased risk of which malignancies?

A
Breast
Ovarian
Lung
Colon
Oesophagus
Bladder
--> screen at time of diagnosis
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9
Q

What are the clinical features of fibromyalgia?

A

Persistent (> 3 months) widespread pain/tenderness
–> both sides of body, above + below waist, including axial spine
Fatigue
Disrupted + unrefreshing sleep
Cognitive difficulties
Other unexplained symptoms e.g. anxiety, depression, functional impairment

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10
Q

Which other conditions is fibromyalgia associated with?

A

Depression
IBS
Migraine

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11
Q

How is fibromyalgia diagnosed?

A

Clinically

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12
Q

How is fibromyalgia managed?

A
Patient education + validation
Graded exercise programme
CBT
Alternative therapies e.g. acupuncture
Atypical analgesics e.g. amitriptyline, pregabalin, gabapentin
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13
Q

What are the clinical features of polymyalgia rheumatica?

A

Proximal myalgia of hip and shoulder girdles
–> muscle strength normal
+ morning stiffness > 1 hour
Tend to improve throughout the day + with movement

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14
Q

Who gets polymyalgia rheumatica?

A

Elderly, very rare < 50 yrs

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15
Q

Which other condition in polymyalgia rheumatica strongly associated with?

A

Giant cell/temporal arteritis

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16
Q

How is polymyalgia rheumatica diagnosed?

A

No specific diagnostic test but

CRP +PV/ESR almost always raised

17
Q

What is the treatment and prognosis for polymyalgia rheumatica?

A

Responds dramatically to low dose steroids (sometimes used as diagnostic tool)
–> prednisolone 15mg daily
Dose gradually reduced over about 18 months
Condition usually resolved by end of this period