muscle disease Flashcards

1
Q

what is the difference between polymyositis and dermatomyositis?

A

same condition, dermatomyositis involves skin too

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the presentation of polymyositis?

A

slow onset, symmetrical, proximal muscle weakness
girdle muscles - hip and shoulders
mild myalgia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is Gotton’s sign?

A

scaly, red/purple papule on PIP and MCP joints

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what is heliotrope rash?

A

lilac rash over eyes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is shawl’s sign?

A

macular rash over back and shoulders

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what systemic features are seen with polymyositis?

A
interstitial lung disease (SOB)
dysphagia 
myocarditis 
fever
weight loss 
raynauds
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what does polymyositis increase your risk of?

A

malignancy

increased risk of breast, ovarian, lung, bladder and bowel

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what test are done to diagnose polymyositis? what are the findings?

A

confrontational testings
isotonic testing (30 secs sit to stand)
muscle power reduced

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is seen on bloods in polymyositis?

A

very elevated CK

anti-jo1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what test is diagnostic in polymyositis?

A

muscle biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what other rest can be done in polymyositis?

A

EMG - increased fibrillations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the management for polymyositis?

A

malignancy screening
steroids - then reduced
DMARDS - methotrexate/azathioprine (take 4-6 weeks to start working)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

if not responding to treatment, what should you consider?

A

inclusion body myositis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what differences are seen in inclusion body myositis?

A

more common in men >50
asymmetrical weakness affecting distal muscles
inclusion bodies on biopsy
CK elevated but not as high as in polymyositis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the symptoms of polymyalgia rheumatia?

A

muscle pain and stiffness
quick onset - few weeks
usually symmetrical
muscle pain in shoulders and hips, not weakness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what does PR have an association with? how does it present?

A
giant cell arteritis 
unilateral headache 
scalp tenderness (sore to brush hair)
TMJ claudication
tender, enlarged temporal artery
visual loss
17
Q

what is seen on bloods in PR?

A

raised inflammatory markers - CRP and ESR

CK normal

18
Q

what other tests can be done for PR?

A

temporal artery biopsy if GCA suspected

19
Q

what is the management for PR?

A

15mg ( low dose) prednisolone
(big response in few days)
temporal arteritis without visual loss 40mg pred
temporal arteritis with vision loss 60mg pred

20
Q

how long is the steroid treatment for PR?

A

18 months - 2 years

gradual reduction