inflamm myopathies Flashcards

(18 cards)

1
Q

what are the types of inflammatory myopathies ?

A

dermatomyositis
polymyositis
inclusion body myositis

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2
Q

common and important risk factor for dermatomyositis ?

A

UV rays

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3
Q

clinical picture of dermatomyositis and polymyositis ?

A

develop over weeks to months
fever and weight loss
non-erosive inflammatory polyarthritis
raynaud’s phenomenon
calcifications in childhood DM

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4
Q

what are the patterns of muscle weakness in PM and DM

A

proximal muscle weakness of the upper limb - unable to comb their hair, can’t take things from a height
proximal muscle weakness of the lower limbs - difficulty getting up from a chair, difficulty climbing up the stairs
pharyngeal and respiratory muscle weakness - dysphagia, breathing problems

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5
Q

what are the skin manifestations of dermatomyositis ?

A

heliotrope rash on eyelids
rash on thee face, neck and chest ( V sign, diffuse and photosensitive )
rash on the back ( shawl sign )
Gottron’s papules - papules and rashes on MCP and IP joints
rough cracked hands - mechanic’s hand
dilated nail bed capillary loops

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6
Q

what is pathognomonic for DM ?

A

gottron’s papules

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7
Q

difference between dermatomyositis and polymyositis ?

A

polymyositis exhibits proximal muscle weakness but no skin manifestations , and is also commonly associated with AV conduction defects and interstitial Lung disease

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8
Q

what malignancies are commonly associated with dermatomyositis ?

A

lung
breast
ovaries
GI
Non-hodgkins

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9
Q

polymyositis may show features of what 2 diseases ?

A

scleroderma and mixed connective tissue disease
so a diagnosis of exclusion

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10
Q

most important method of diagnosis of DM and PM ?

A

muscle biopsy

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11
Q

what are the steps or algorithm that a patient must go for a diagnosis of DDM or PM ?

A

patient presented with proximal muscle weakness
heliotrope rash , v sign, shawl sign ( in DM)
perform CK , AST , ALT LDH , aldolase
abnormal EMG

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12
Q

treatment for PM and DM ?

A

prednisone 0.5-1 mg/kg
- muscle enzymes may improve but muscle strength takes longer
give biphosphonates

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13
Q

patient diagnosed with PM or DM , but not responding to steroids and has developed distal muscle weakness as well as proximal - what is the most likely diagnosis ?

A

inclusion body myositis

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14
Q

in what group of patients in inclusion body myositis seen in ?

A

males abovee thee age of 50

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15
Q

what is the pattern of muscle weakness in inclusion body myositis ?

A

bilateral
asymmetrical distal and proximal muscle weakness

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16
Q

what aree thee medicatioins that can cause muscle weakness ?

A

amiodarone
antithyroid agents
antiretroviral - HIV patients

17
Q

which patients should we think twice in before diagnosing an inflammatory myopathy ?

A

thyroid patients
patients with arrythmia
HIV positive patients

18
Q

what are the differential metabolic causes of muscle weakness ?

A

glycogen and lipid storage disease
mitochondrial disease
hypokalaemia
hypercalcaemia