Vasculitis Flashcards

(60 cards)

1
Q

What is vasculitis?

A

Inflammation of blood vessels

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2
Q

How can vasculitis be classified? (2)

A
  • Size of vessel
  • ANCA positive or negative
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3
Q

What are the two major categories of large vessel vasculitis?

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

Which arteries are most common for giant cell arteritis to affect?

A
  • Temporal artery (most common)
  • Opthalmic artery
  • Facial artery
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5
Q

The endothelium is generally directly attacked with molecular mimicry in which two classes of vasculitis?

A
  • Large vessel
  • Medium vessel
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6
Q

The endothelium is generally indirectly attacked in which class of vasculitis?

A

Small vessel

(N.b Henloch-Scholein purpura is an exeption to this rule)

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7
Q

What happens to the vessel walls due to the inflammation is vasculitis?

A
  • Inflammatory processes cause tissue factor and collagen to be exposed (endothelial cells die)
  • Thrombosis occurs
  • Vessel walls weak leading to aneurysm
  • Fibrosis due to fibrin deposition occurs as part of the healing process
  • Both thrombosis and fibrosis narrow the vessel lumen reducing blood flow
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8
Q

Ultimately, vasculitis leads to less ______ _____

A

Bloof flow

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9
Q

Why does jaw claudication occur with giant cell arteritis?

A

The facial artery is affected and less blood flow to the face occurs

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10
Q

Giant cell arteritis is most common in what age group and sex?

A

Women > 50

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11
Q

What is found in the elastic lamina in a patient with giant cell arteritis?

A

Granulomas or “giant cells”

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12
Q

When taking a biopsy for giant cell arteritis, why is a negative result not able to rule out the condition?

A

Giant cell arteritis is segmental

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13
Q

Takayasu arteritis is most common in which age group and sex?

A

Asian women < 40

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14
Q

Takayasu arteritis generally affects which arteries?

A

Those off of the aortic arch

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15
Q

In patients with Takayasu arteritis, what is found in the internal elastic lamina?

A

Granulomas or “giant cells”

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16
Q

What are some common medium vessel arteritides?

A
  1. Kawasaki disease
  2. Polyarteritis nodosa
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17
Q

Kawasaki disease generally affects people of what age?

A

< 5

(boys more than girls)

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18
Q

What are the symptoms of Kawasaki disease?

A

Conjuctivitis (sparing the limbus)

Rash over body

Adenopathy (large or swollen lymph nodes)

Strawberry tongue

Hands and feet swelling

Fever

(Patients crash and burn)

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19
Q

Kawasaki disease is usually _____ __________

A

Self limiting

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20
Q

How can Kawasaki disease be treated?

A

IV Ig

Aspirin (monitor very closely for Reye syndrome)

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21
Q

What is the pathogenesis behind polyarteritis nodosa?

A

Immune cells directly attack the endothelial cells

This is an example of molecular mimicry as the antibodies produced are designed to takle hepatitis B

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22
Q

Polyarteritis nodosa causes ___________ necrosis

A

Transmural

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23
Q

Fibrinoid necrosis occurs with polyarteritis nodosa which leaves the vessels prone to what?

A

Aneurysm

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24
Q

Upon angiogram, polyarteritis nodosa has a very distinctive appearance. What is this appearance?

A

“String of beads”

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25
In polyarteritis nodosa what happens when renal arteries are affected?
Hypertension (low glomerular pressure leads to fluid retention and increased blood pressure)
26
What can occur when the mesenteric arteries are affected in polyarteritis nodosa?
* Abdominal pain * GI bleed
27
What is Buerger's disease?
A medium vessle vasculitis affecting vessels in the fingers and toes Blood clots occur as a result leading to ulceration, necrosis and auto-amputation of the fingers and toes
28
What is a major risk factor and potential trigger for Buerger's disease
Use of tobacco
29
What is ANCA?
Anti-neutrophil cytoplasmic antibody
30
Wegener's granulomatosis (Granulomatosis with polyangiitis) involves which type of ANCA?
cANCA | (cytoplasmic ANCA)
31
In Wegener's granulomatosis, cANCA binds to what?
Proteinase 3 within the neutrophilic membrane
32
When pANCA or cANCA binds to neutrophils, why does the endothelium end up damaged?
O2 free radicals are released from neutrophils causing indirect damage
33
Name some small vessel vasculitides?
* Wegener's granulomatosis * Microscopic polyangiitis * Churg-Strauss syndrome * Henloch-Schonlein purpura * Renal limited vasculitis
34
Wegener's granulomatosis is more common in which sex?
Men
35
Which areas of the body does Wegener's granulomatosis commonly affect?
Nasopharynx (painful sinusitis, bloody mucous from ulcers and saddle nose deformity) Lungs (difficulty breathign due to ulcer formation and bloody cough) Kidneys
36
Saddle nose deformity is associated with which vasculitis?
Wegener's granulomatosis
37
Once cured, relapse of Wegener's granulomatosis is what?
Common
38
How is microscopic polyangiitis different from Wegener's granulomatosis?
1. Does not affect nasopharynx (only kidneys and lungs) 2. No granulomas can be found in vessle walls 3. pANCA vs cANCA
39
What is pANCA?
Perinuclear ANCA
40
After microscopic polyangiitis is cured or overcome, relapse is what?
Common
41
Churg-Strauss syndrome is commonly mistaken for what?
Asthma or allergies
42
Which immune cell type is particularly elevated in Churg-Strauss syndrome?
Eosinophils
43
Which areas of the body does Churg-Strauss syndrome affect?
* Sinuses * Lungs * Kidneys * GI tract * Skin * Nerves * Heart
44
Are granulomas associated with Churg-Strauss syndrome?
Yes
45
What makes Henloch-Schonlein purpura different from other small vessel vasculitides?
There are no ANCAs involved
46
What causes Henloch-Schonlein purpura?
IgA targets endothelial cells via molecular mimicry
47
The purpura seen in Henloch-Schonlein purpura is distinctive, but why?
It is palpable This is due to the fibrosis occurng in the affected vessels
48
Henloch-Schonlein purpura can affect two other major body systems besides the skin, what are these?
GI (abdominal pain) Renal (haematuria, IgA nephropathy)
49
Henloch-Schonlein purpura can resolve on its own. True or false?
True
50
Large vessel vasculitis can lead to reduced _______ and carotid \_\_\_\_\_\_\_\_
Pulses Bruit
51
What is the treatment for large vessle vasculitis?
40-60mg of prednisolone which granually reduces
52
What is the most common complication of microscopic polyangiitis?
Glomerulonephritis
53
Most cases of ANCA +ve vasculitis require what treatment?
IV steroids Cyclophosphamide
54
Henloch-Schonlein purpura commonly affects children and a history involving what is common?
An upper respiratory tract infection predating symptom onset by a few weeks
55
Henloch-Schonlein purpura has what symptoms commonly?
* Purpuric rash over buttocks and lower limbs * Abdominal pain * Vomiting * Joint pain
56
Henloch-Schonlein purpura requires what treatment?
It is a self limiting condition which does nto require much specific treatment It will settle over a period of weeks to months
57
Temporal arteritis has a common association with what?
Polymyalgia rheumatica
58
cANCA and anti-PR3 are asscoiated with what?
Wegener's granulomatosis
59
pANCA and anti-MPO are associated with what?
Microscopic polyangiitis
60
Anti-MPO or anti-PR3 are asscoiated with what?
Churg-Strauss syndrome (Eosinophilic granulomatosis with polyangiitis)