Muscle Diseases Flashcards

1
Q

how do muscle diseases present

A

myalgia (muscle pain)
muscle weakness/tiredness
stiffness
abnormal blood tests

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2
Q

what type of myopathy are polymyositis and dermatomyositis

A

idiopathic inflammatory myopathies

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3
Q

who is more likely to get polymyositis and dermatomyositis

A

females 2 : males 1

40-50 years

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4
Q

what there an increased incidence of in patients with polymositis and dermatomyositis

A

malignancy

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5
Q

what is seen histologically in polymyositis and dermatomyositis

A

muscle biopsy: muscle fibre necrosis, degeneration, regeneration and an inflammatory cell infiltrate.
perivascular necrosis

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6
Q

what are the clinical features of idiopathic inflammatory myopathy (polymyositis and dermatomyositis)

A

MUSCLE WEAKNESS

insidious onset, worsening over months
usually symmetrical, proximal muscles

myalgia in 25-50%

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7
Q

what extra features distinguish the clinical presentation of dermatomyositis from polymyositis

A

cutaneous signs

  • gottrons sign
  • heliotrope rash
  • shawl sign
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8
Q

what other organs can be involved in inflammatory myositis

A

lung (ILD, resp muscle weakness)

oesophagus (dysphagia

cardiac (myocarditis)

also:
fever, weight loss, raynauds, non-erosive polyarthritis)

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9
Q

what cancers are associated with inflammatory myositis

A

ovarian, breast, stomach, lung, bladder and colon cancer

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10
Q

in a history of a patient with an inflammatory myositis, what are other common medical problems

A

Dermatomyositis, thyroid disease, raynauds

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11
Q

what is isotonic testing

A

30 second sit to stand test

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12
Q

what tests can be included to test muscle function

A

confrontational testing- tests direct power

isotonic testing

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13
Q

what blood tests can be done into inflammatory myositis

A

muscle enzymes- creatine kinase (CK)
inflammatory markers
electrolytes, calcium, PTH, TSH (to exclude other causes)
autoantibodies (ANA, Anti-Jo-1)

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14
Q

what is seen in electromyography in inflammatory myositis

A

increased fibrillations
abnormal motor potentials
complex repetitive discharges

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15
Q

what is the definitive test for inflammatory myositis

A

muscle biopsy

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16
Q

what is seen in biopsy of inflammatory myositis

A

muscle inflammation,
oedema,
fibrosis,
calcification

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17
Q

what is the treatment for idiopathic inflammatory myosisitis (polymyositis and dermatomyositis)

A
glucocorticoids
azathioprine 
methotrexate
ciclosporin 
IV immunoglobulin 
rituximab
18
Q

what medication might cause a similar presentation to myositis

A

atorvastatin

19
Q

what is polymyalgia rheumatica

A

idiopathic inflammatory condition associated with temporal arteritis/ giant cell arteritis

20
Q

who gets polymyalgia rheumatica

21
Q

what is the clinical presentation of polymyalgia rheumatica

A

ache in shoulder and hip girdle

morning stiffness

usually symmetrical

fatigue, anorexia, weight loss, fever

reduced movement of shoulders, neck and hips

22
Q

what is muscle strength like in polymyalgia rheumatica

23
Q

what is temporal arteritis/ giant cell artheritis

A

granulomatous arteritis of large vessels

24
Q

what are the symptoms of temporal arteritis/ giant cell arteritis

A

headache, scalp tenderness, jaw claudication, visual loss, tender, enlarged, non pulsatile temporal arteries

25
how do you diagnose temporal arteritis/ (GCA)
raised ESR, plama viscosity, CRP temporal artery biopsy
26
how do you treat temporal arteritis/ GCA
steroids (prednisolone 40mg, 60mg if visual impairment)- gradually reduced over around 18 months to 2 years steroids as a diagnostic tool- Symptoms respond very dramatically to low dose steroids (prednisolone 15mg daily)
27
what is fibromyalgia
idiopathic chronic (MSK) pain disorder
28
is fibromyalgia associated with inflammation
no
29
who gets fibromyalgia
females 6 : males 1 | 22-50 y/o
30
when does fibromyalgia pain sometimes begin
after emotional or physical trauma
31
what is the pathology of fibromyalgia
dorsal horn neurones become hyperresponsive to nociceptive and nonnociceptive somatic senation due to extracellular Ca+ and nitric acid diffusing into neurones resulting in exaggerated release of sustance P and glutamate = hyperalgesia
32
what are the clinical manifestations of fibromyalgia
pain; neck, shoulders, lower back, chest wall diffuse and chronic, varies in intensity symptoms worse with exertion, fatigue and stress sensation of swelling, fatigue, poor, unrefreshing sleep pins and needles/ tingling, headaches, depression, abdominal pain (IBS), poor concentration and memory
33
what are the clinical findings in fibromyalgia
excessive tenderness on palpation of soft tissues 11/18 tender points no abnormalities of MSK system
34
what is the treatment for fibromyalgia
education exercise programme congitive behavioural therapy complemetary medicine (acupuncture) anti depressants (tricylics- amitriptyline) analgesia gabapentin and pregabalin
35
does morphine help in fibromyalgia
no
36
what is pain of the shoulder and hips without weakness in in 70s
polymyalgia rheumatica
37
what condition commonly co exists with PMR
giant cell vacsulitis
38
what responds rapidly to steroids
PMR
39
what is CK raised in
polymyositis only (and dermomyositis
40
what anti body for polymyositis
anti jo 1
41
what palpation can show firbomyalgia
excessive tenderness of palpation of soft tissue in 11 out of 18 sites
42
what is difficulty climbing the stairs a sign of
polymyositis