Vasculitis Flashcards

1
Q

List 4 types of vasculitis which affect the small sized vessels

A
  1. Henoch-Schonlein purpura
  2. Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss syndrome)
  3. Microscopic polyangiitis
  4. Granulomatosis with polyangiitis (Wegener’s granulomatosis)
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2
Q

List 3 types of vasculitis which affect the medium sized vessels

A
  1. Polyarteritis nodosa
  2. Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss syndrome)
  3. Kawasaki Disease
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3
Q

List 2 types of vasculitis which affect the large sized vessels

A
  1. Giant cell arteritis
  2. Takayasu’s arteritis
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4
Q

List 4 features of a vasculitis

A
  1. Purpura
  2. Joint and muscle pain
  3. Peripheral neuropathy
  4. Renal impairment
  5. GI disturbance (diarrhoea, abdominal pain and bleeding)
  6. Anterior uveitis and scleritis
  7. Hypertension
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5
Q

List 4 systemic manifestations of vasculitis

A
  • Fatigue
  • Fever
  • Weight loss
  • Anorexia (loss of appetite)
  • Anaemia
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6
Q

Specific test findings for vasculitis

A
  1. ANCA (p-ANCA and c-ANCA)
  2. ↑CRP and ESR
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7
Q

Compare pANCA vs cANCA

A

p-ANCA (MPO antibodies): Microscopic polyangiitis and Churg-Strauss syndrome

c-ANCA (PR3 antibodies): Wegener’s granulomatosis

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8
Q

What is Henoch-Schonlein Purpura?

A

An IgA vasculitis that commonly presents with a purpuric rash affecting the lower limbs or buttocks in children (< 10 yrs)

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9
Q

Most common cause of HSP?

A

Often triggered by an upper airway infection (e.g. tonsillitis) or a gastroenteritis

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10
Q

Four classic features of HSP?

A
  1. purpura (100%)
  2. joint pain (75%)
  3. abdominal pain (50%)
  4. renal involvement (50%)
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11
Q

Management of HSP

A

Supportive ie. simple analgesia, rest and proper hydration

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12
Q

How does Eosinophilic granulomatosis with polyangiitis commonly present?

(Churg-Strauss syndrome)

A

Presents with severe asthma in late teenage years or adulthood

Most associated with lung and skin problems

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13
Q

Characteristic finding on FBC of Churg-Strauss syndrome

A

↑ eosinophil levels

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14
Q

Main feature of Microscopic polyangiitis

A

Renal failure

(can also affect the lungs causing SOB and haemoptysis)

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15
Q

Classic presentation/features of Wegener’s granulomatosis?

(Granulomatosis with polyangiitis)

A
  1. Epistaxis and crusty nasal secretions
  2. Hearing loss and Sinusitis
  3. Saddle shaped nose due to a perforated nasal septum
  4. Cough, wheeze and haemoptysis
  5. Glomerulonephritis
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16
Q

What is Polyarteritis Nodosa?

A

Medium vessel vasculitis associated with hepatitis B

Associated with a rash called livedo reticularis. - mottled, purplish, lace like rash

17
Q

What is Kawasaki Disease

A

Medium vessel vasculitis which affects young children (< 5) with no clear cause

18
Q

Clinical features of Kawasaki Disease

A
  1. Persistent high fever > 5 days
  2. Erythematous rash
  3. Bilateral conjunctivitis
  4. Erythema and desquamation (skin peeling) of palms and soles
  5. Strawberry tongue
19
Q

Key complication of Kawasaki Disease

A

coronary artery aneurysms

20
Q

Treatment of Kawasaki Disease

A

Aspirin and IV immunoglobulins

21
Q

What is Takayasu’s arteritis?

A

Large vessel vasculitis which mainly affects the aorta and it’s branches. It also affect the pulmonary arteries.

These can swell and form aneurysms or become narrowed and blocked which leads to it’s other name of “pulseless disease

22
Q

How does Takayasu’s arteritis?

A
23
Q

How does Takayasu’s arteritis present?

A

Before 40 years with:

  • Non-specific systemic symptoms: fever, malaise and muscle aches
  • Specific symptoms: arm claudication or syncope
24
Q

How is Takayasu’s arteritis diagnosed

A
  1. CT or MRI angiography
  2. Doppler ultrasound of the carotids can be useful in detecting carotid disease