Vasculitis Flashcards

1
Q

What soft tissue condition is Temporal arteritis (giant cell arteritis) associated with?
What are the typical symptoms and signs of Temporal arteritis?

A

Polymyalgia rheumatica

Temporal headache
Scalp tenderness
Jaw claudication
Prominent arteries with reduced pulsation

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2
Q

What is vasculitis?

A

inflammation of blood vessels

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3
Q

What are the two important causes of large vessel vasculitis?

A

Giant cell arteritis (GCA)

Takayasu arteritis (TA)

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4
Q

Takayasu arteritis tends to affect what patients?

A

female
under 40
asian

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5
Q

What arteries are commonly affected by Giant Cell Arteritis?

What patients are typically affected?

A

temporal arteries

patients over 50

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6
Q

What clinical signs are common in Large Vessel Arteritis?

A
Carotid artery bruit
Difference in blood pressure of extremities
Claudication
Vessel tenderness
Hypertension
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7
Q

Temporal arteritis (giant cell arteritis) can cause blindness. (T/F)

A

True

-due to ischaemia of the optic nerve

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8
Q

What is the treatment of Giant Cell Arteritis?

A

High does steroids (40-60mg Prednisolone)

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9
Q

Kawasaki disease is a ______ vessel vasculitis which can lead to aneurysm formation in ______ arteries.

A

medium vessel

coronary arteries

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10
Q

What medium vessel vasculits is associated with hepatitis B and affects skin, gut and kidneys.

A

Polyarteritis nodosa

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11
Q

Granulomatosis with polyangitis (GPA) is a small vessel vasculitis, which typically presents at age 35-55 years.
What organs are affected?

A

ENT

  • saddle nose
  • mouth ulcers
  • sinusitis
  • nose bleeds
  • deafness

Lungs
-pulmonary infiltrates
and cavitating nodules on CXR
-cough and haemoptysis

Skin

  • palpable purpuric rash
  • ulcers

Kidneys
-necrotising glomerulonephritis (blood and protein in urine)

Nervous system

  • peripheral neuropathy
  • cranial nerve palsies (eye)

Eye
-uveitis, conjunctivitis

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12
Q

Eosinophilic Granulomatosis with Polyangitis (EGPA) is similar to Granulomatosis with Polyangitis (GPA). What features of GPA are present less in EGPA?

A

ENT symptoms

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13
Q

What respiratordy condition is often present in EGPA (eosinophilic granulomatosis with polangitis)?

A

Late onset asthma

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14
Q

Granulomatosis with Polyangitis (GPA) is associated with what antibodies?

A

cANCA

PR3

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15
Q

What antibodies are detected in EGPA (eosinophilic granulomatosis with polangitis)?

A

pANCA

MPO

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16
Q

Nasal carriage of Staph areus is a risk factor for ANCA-associated small vessel vasculitis (T?f)

A

True

17
Q

What is the treatment of GPA and EGPA (ANCA-associated vasculitis)?

A

Cyclophosphamide + Steroids

18
Q

Henoch-Schonlein Purpura (HSP) is mediated by __. The vasculitis involves ____ vessels of the skin, GI tract, kidneys and joints.

A

IgA

small vessels

19
Q

How does Henoch-Schonlein Purpura present?

A

Purpuric rash over buttocks and lower limbs

  • colicky abdo pain
  • bloody diarrhoea
  • joint pain
  • renal involvement