Muscle Diseases Flashcards

1
Q

What are two signs of polymyalgia rheumatic?

A

Pain and stiffness.

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

Where does polymyalgia rheumatica present?

A

Shoulder and hip girdles.

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

How long does morning stiffness present for in polymyalgia rheumatic?

A

Lasts for over an hour.

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

What condition is strongly associated with polymylagia rheumatic?

A

Giant Cell Arteritis

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

What is base line treatment for PMR with no giant cell arteritis?

A

15mg prednisolone daily

responds very rapidly <24 hours

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

PMR What is the length of the prednisolone course.

A

18 months and the dosage is gradually reduced over that period.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Giant cell arteritis pathology

A

Inflammation of vessel walls with immune infiltration.

Thickening results I luminal narrowing and subsequent distal ischaemia.

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

Giant Cell Arteritis

Presentation

A
Unilateral acute temporal headaches.
Scalp tenderness
Visual disturbances
Jaw claudication
Prominent non pulsatile temporal artery.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Main risk of GCA

A

Blindness due to ischaemia of optic nerve.

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

What artery results in jaw claudication?

A

Maxillary Artery

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

GCA Diagnosis

A

Raised plasma viscosity and CRP
MR/CT angiogram
Temporal artery biopsy is gold standard.

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

What cells on biopsy are seen to have infiltrated the vessel walls.

A

Lymphocytes macrophages and multinucleate giant cells

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

Treatment for GCA with no visual impairment?

A

40mg of prednisolone

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

Treatment of GCA with visual impairment?

A

60mg of prednisolone

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

Period of prednisolone treatment in GCA?

A

Over 2 years gradually decreasing.

Treatment started as soon as diagnosis suspected DON’T wait for biopsy result.

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

Muscle tone is polymyalgia reumatica?

A

Reduced muscle movement but strength is normal.

17
Q

In polymyalgia rheumatica what is commonly used as a diagnostic tool?

A

15mg dose of prednisolone due to rapid response.

18
Q

Other symptoms related to polymyalgia rheumatic?

A

Systemic

Fatigue, anorexia, weight loss and fever

19
Q

What is Polymyositis?

A

Idiopathic inflammatory myopathy.

2:1 F:M 40-50 years usually

20
Q

What is dermatopolymyositis?

A

Clinically very similar to polymyositis but with skin involvement.

21
Q

Pathogenesis behind polymyositis?

A

T-cell mediated necrosis of muscle fibres.

22
Q

What antibodies are associated with polymyositis?

A

anti-Jo-1

anti-SRP

23
Q

Presentation of polymyositis

A

Symmetrical and proximal gradual muscle weakness.
Often described by inability to perform actions which were once easy.
Up to half of patients will have myalgia.

24
Q

Systemic symptoms of polymyositis

A

Lung- Interstitial lung disease, generally pulmonary fibrosis
- respiratory muscle weakness
Oesophageal- dysphagia
Cardiac- Myocarditis
Systemic - Fever weight loss, raynauds, inflammatory arthritis.

25
Q

What is there an increased risk of in dermatomyositis?

A

Malignancy specifically ovarian breast and bowel.

26
Q

Who are at most risk of malignancy in dermatomyositis?

A

Men over 50 years old.

27
Q

Investigations for polymyositis

A

MRI- shows oedema and scarring
FBC
Electromyograph- abnormal finding low voltage short duration.
Biopsy- gold standard
- shows varying degrees of inflammation and necrosis

28
Q

Full blood count and immunology findings in polymyositis?

A

Raised CRP and plasma viscosity.
Serum creatinine kinase levels increased showing muscle breakdown.
ANA, anti-JO-1 and anti-SRP

29
Q

Polymyositis treatment

A

Prednisolone usually 40mg combined with methotrexate azathioprine etc

30
Q

What other features are typical of dermatomyositis?

A

Shawl sign - V-shaped rash over chest
Gottrons papules- rash over MCP joints and back of hands.
Heliotrope Rash- Rash around the eyes.

31
Q

Fibromyalgia

A

Chronic widespread muscle pain and fatigue. Common in young and middle aged women.

32
Q

Name some triggers for fibromyalgia

A

IBS emotional or physical trauma , lights sounds heat etc

33
Q

Pathogenesis of fibromyalgia

A

Unknow, but thought to be an abnormality in pain processing and sensitivity due to biochemical metabolic or immunological reasons.

34
Q

What conditions are often linked to fibromyalgia?

A

Systemic Lupus Erythematosis

Rheumatoid arthritis

35
Q

Presentation of fibromyalgia

A

Persistant and widespread pain >3 months.
Fatigue with disrupted and unrefreshing sleep.
Cognitive impairment ‘fuzzy brain’
Anxiety depression

36
Q

Are there any investigations in fibromyalgia?

A

No its based entirely of clinical bases however tests must be conducted to outrule clinically similar conditions.

37
Q

What conditions can present like fibromyalgia?

A

Hypothyroidism, rheumatoid arthritis, systemic lupus erythematosus.

38
Q

Management of fibromyalgia

A

Education in self management and exercise.
Validating concerns and acknowledgment of patients pain.
Counselling and behavioural therapy.
Analgesia

39
Q

What analgesics are used in fibromyalgia?

A

Gabapentin Pregabalin and amitriptyline.