Vasculitis Flashcards

1
Q

Define vasculitis

A

Inflammation of blood vessels

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2
Q

What does inflammation of blood vessels lead to?

A

Thickening, stenosis, occlusion with ischaemia and necrosis

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3
Q

What can cause secondary vasculitis?

A

Drugs, toxins, infection, disease

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4
Q

How is vasculitis classified?

A

Large vessel
Medium vessel
Immune complex small vessel
ANCA positive small vessel

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5
Q

What are the two types of large vessel vasculitis?

A

Takayasu and Giant Cell

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6
Q

What are the two types of medium vessel vasculitis?

A

Polyarteritis nodosa and kawasaki disease

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7
Q

What are the three types immune small vessel vasculitis?

A

Cryoglobulinemic vasculitis
IgA vasculitis
Hypocomplemtemic urticarial vasculitis

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8
Q

Name the ANCA positive small vessel vasculitis’s

A

Granulomatous with polyangitis

Eosinophilic granulomatosis with polyangitis

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9
Q

What is meant by the term large vessel vasculitis?

A

Granulomatous inflammation of aorta and major branches

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10
Q

Describe the epidemiology of Takayasu arterities

A

Common in eat asian countries usually patients <50 years old

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11
Q

Describe the epidemiology of Giant Cell arterities

A

Associated with polymyalgia rheumatica patients >50 years old

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12
Q

What vessels are commonly affected in giant cell arteritis?

A

Cranial/temporal/ophthalmic/facial arteries

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13
Q

What are the early features of large vessel vasculitis?

A
Fever
Malaise 
Night Sweats 
Weight loss 
Arthralgia 
Fatigue 
Headache (temporal)
Blindness (ophthalmic)
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14
Q

What happens in the late stages of large vessel vasculitis?

A

Claudication - stenosis - aneurysms

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15
Q

What are the clinical signs of late stage large vessel vasculitis?

A

Reduced pulse and bruits

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16
Q

How is large vessel vasculitis diagnosed?

A

ESR, PV and CRP will be elevated
MR angiography shows thickened vessel wall and stenosis
PE CT scan
Ultrasound

17
Q

How is large vessel vasculitis treated?

A

40-60mg Prednisolone gradually reduced

18
Q

What are the clinical features of small vessel vasculitis?

A
  • fever and weight loss
  • raised non-blanching rash
  • arthralgia/arthritis
  • mononeuritis multiplex
  • glomerulonephritis
  • lung opacities
19
Q

What is another name for eosinophilic granulomatosis with polyangitis?

A

Chung-Strauss

20
Q

Describe eosinophilic granulomatosis with polyangitis

A

Characterised by late onset asthma, rhinitis and eosinophilia. Commonly presents with neurological symptoms e.g neuritis multiplex

21
Q

What is another name for granulomatosis with polyangiitis?

A

Wegener’s

22
Q

Describe granulomatosis with polyangitis

A

Inflammation involving the respiratory tract and necrotising vasculitis. Common causes ENT and respiratory symptoms e.g haemoptysis and saddle nose

23
Q

How does microscopic polyangiitis often occur?

A

Common complication of glomerlonerphitis

24
Q

What investigations are carried out for small vessel vasculitis?

A
ESR, CRP and PV
Full blood count and U/Es
ANCA
Urinalysis (assesses renal involvement)
CXR 
Biopsy
25
What is ANCA?
Anti-neutrophilic cytoplasmic antibody - B cells produced antibodies to neutrophils
26
How is small vessel vasculitis treated?
IV Steroids and Cyclophosphamide
27
What is Henoch Schnlein Purpura?
Acute IgA mediated disorder characterised by vasculitis involving; skin, GI tract, kidneys, joints, lungs, CNS
28
How does Henoch Schnlein Purpura present?
Purpuric rash over the bum and lower limbs Abdominal pain Vomitting Joint pain
29
Who is commonly affected by Henoch Schnlein Purpura and how is it treated?
Children with a history of upper respiratory tract infection - self limiting settles in a few weeks