Muscle Disease Flashcards

1
Q

What does “Myalgia” mean?

A

Muscle Pain

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2
Q

What does “My arms feel heavy and tired, i struggle to do things” imply about the muscle?

A

Muscle Weakness

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3
Q

What does “My muscle are stiff when i first wake up and then get a bit better when I’ve walked about for a bit” imply about the muscle?

A

Inflammation

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4
Q

Which muscle disease(s) have an increased risk of malignancy associated?

A

Myositis

especially dermatomyositis

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5
Q

What type of disease are Polymyositis and Dermatomyositis?

A

Idiopathic Inflammatory Myopathies

Autoimmune

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6
Q

Who’s more like to get polymyositis? (male/female) (ages 10-20/ 20-30/30-40/40-50/50-60/60-70/65+)

A

Females (2:1)

40-50 years peak

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7
Q

What is seen on biopsy of Polymyosits?

A

Muscle fibre necrosis
Degeneration
Regeneration
An inflammatory cell infiltrate

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8
Q

What is the most common presenting complaint of a patient with polymyosits?

A

Muscle weakness

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9
Q

List some clinical features of Myositis:

A

Muscle weakness
Insidious onset, worsening over months.
Usually symmetrical, proximal muscles
Mild myalgia in some patients (25-50%)

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10
Q

Was cutaneous signs are seen in dermatomyositis?

A
Gottron's sign (hands)
Heliotrope rash (face/eyes) (purple/pink discoloration and swelling)
Shawl Sign (Back)
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11
Q

Which drugs are known to cause proximal muscle weakness?

A

Steroids

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12
Q

What other presentations can be important to pick up in a history of tired muscles and functional difficulty?

A
Raynauds Phenomenon
Weight loss
Cough
Breathlessness
Dysphagia
Fever
Non-erosive Polyarthritis
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13
Q

What is the difference between Confrontational Testing and Isotonic Testing?

A
Confrontational = Direct testing of power (pushing)
Isotonic = Repeated movement (e.g. 30 second sit to stand)
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14
Q

Which is a better test of muscle power? (Confrontational, Isotonic)

A

Isotonic testing

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15
Q

Why are Creatine Kinase enzymes raised in Myositis?

A

Muscle inflammtion and breakdown of muscle causes release of muscle enzymes during break down. Creatine Kinase is a muscle enzyme so levels of this rise (up into thousands) in myositis

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16
Q

What is a specific antibody of polymyositis and drmatomyositis?

A

Anti-Jo-1

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17
Q

What is an EMG?

A

Electromyography

Shows pattern of how muscle conducts electricity

18
Q

What is seen on an EMG of a patient with polymyositis?

A

Increased fibrillations, abnormal motor potentials, complex repetitive discharges

19
Q

Treatment for Myositis:

A

Prednisolone daily - decrease dose over time
Use immunosuppression at same time as steroid
(steroids - short term)

20
Q

What is typical of Inclusion body myositis?

A

Distal muscle weakness
Weakness wrist and finger flexors in upper limbs and quadriceps and anterior tibial muscles in legs
Weakness often asymmetrical
Patients >50

CK levels lower than polymyositis
Muscle biopsy shows inclusion bodies
Responds poorly to therapy

21
Q

How high are the CK levels in IBM and PM?

A

High
(Not up into thousands in IBM)
(Into thousands in PM, much higher)

22
Q

What is the best test for myositis?

23
Q

What are the main symptom of myositis?

A

Muscle Weakness

24
Q

Which drugs may cause a presentation similar to myositis?

25
Who gets Polymyalgia Rheumatica? (age) (Almost exclusively)
Over 50 year olds
26
What condition is associated with Polymyalgia Rheumatica?
Temporal Arteritis/ Giant Cell Arteritis (15%)
27
What are the clinical manifestations of Polymyalgia Rheumatica?
Ache in shoulder and hip girdle Morning stiffness Usually symmetrical Fatigue, anorexia, weight loss and fever may occur Reduced movement of shoulders, neck and hips due to pain and stiffness Comes on quite quickly (within a few weeks) Worst first thing in the mornign Struggle to get out of bed Better after walking about a bit MUSCLE STRENGTH NORMAL
28
Whats "the fear" with GCA (temporal arteritis)?
Blindness
29
What would be raised in polymyalgia rheumatica?
ESR, plasma viscosity, CRP
30
Is polymyalgia rheumatica autoimmune?
NO | INFLAMMATORY CONDITION
31
Treatment for polymyalgia rheumatica: | no temporal arteritis
15mg Prednisolone | feel dramatically better
32
Treatment for polymyalgia rheumatica: | WITH temporal arteritis
40-60mg Prednisolone | to prevent visual loss
33
Is fibromyalgia an inflammatory or non-inflammatory problem?
Non-inflammatory
34
Main symptoms of Fibromyalgia:
Pain Extreme fatigue Poor sleep pattern
35
Does exercise make symptoms of fibromyalgia better or worse?
Worse
36
Where is the pain in fibromyalgia?
Neck Shoulder Lower back Chest wall
37
What is fibromyalgia pain like?
``` Diffuse Chronic Varies in intensity Worse with exertion, fatigue, stress Sensation of swelling ```
38
How many tender points need to be present to make a diagnosis of fibromyalgia?
11 out of 18
39
Are the inflammatory markers raised in fibromyalgia?
No They are normal It is a non-inflammatory
40
Treatment for Fibromyalgia:
Better to not give medication initially Try to minimise drugs Use non-drug therapies, e.g. CBT, graded exercise Start with Paracetamol, then Amitrptyline