myopathies Flashcards
drugs that can cause myopathy
steroids
alcohol
statins
inflammatory myopathies -
polymyositis
dermatomyositis
Inclusion body myositis
Poly+dermatomyositis: cause = F:M age of peak incidence increased\_\_\_ risk
idiopathic
F2:1M
40-50yo
malig
histology of poly+dermatomyositis
muscle fibre necrosis
degeneration
regeneration and inflammatory infliltrate
cutaneous signs in dermatomyositis
Gottrons sign (back of hands)
heliotrope rash
shawl sign
poly+dermatomyositis usually have an ___ onset
worsen over ___ and main feature = ___ - only 25-50% have ___
usually a/symmetrical? and ___ muscles
insidious months muscle weakness mild myalgia asymmetrical proximal
other organ involvement in poly+dermatomyositis
ILD10%, resp muscle weakness dysphagia myocarditis fever wt loss Raynauds nonerosive polyarthritis
malignancies ass with poly and dermatomyositis
most at risk pop group =
which is more ass with malig?
ovarian, breast, stomach, lung, bladder + colon
M >45yo
dermatomyositis
examination tests for poly/dermatomyositis
muscle wasting
rashes
confrontational test (direct power test)
isotonic testing ( repeat stand and sit for 30s - use to monitor)
endomyseal inflammation with CD8+ cells
polymyositis
perimyseal inflammation with CD4+ cells and perifascicular atrophy
dermatomyositis
Ix for poly+dermatomyositis
bloods - CK, inflam markers, electrolytes, Ca2+, PTH and TSH, ANA and Anti Jo-1
EMG
MRI
muscle biopsy (definitive)
results of blood tests in poly+dermatomyositis
CK in the 1000s (v high)
inflam markers high
ANA and anti-Jo1 maybe
results of EMG in poly+dermatomyositis
increased fibrillations
abnormal motor potentials
complex repetitive discharges
MRI results in early and late poly+dermatomyositis
early = muscle inflam and oedema late = fibrosis and muscle calcification