Vasculitis Flashcards

(28 cards)

1
Q

How can vasculitis be classified?

A

Into the vessel size affected- small, medium and large

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2
Q

What are the small vasculitis?

A

Granulomatous with polyangitis
Microscopic polyangitis
Churg strauss
Henloch Scholein Purpura

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3
Q

What are the medium cell vasculits?

A

Kawaski disease
Polyarteritis nodosa
Beurgers disease

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4
Q

What are the large vessel vasculitis?

A

GCA and Takayasu

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5
Q

How can small vessel vasculitis be further split?

A

ANCA associated - microscopic polyangitis, Wergeners and Churg strauss
Immunological associated - Goodpastures disease, IgA vasculitis

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6
Q

What is the general management for vascultiis?

A

Large - steriods

Medium and small - immunosuppression

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7
Q

What is polyarteritis nodosa?

A

Necrotsing vasculitis that causes aneurysms and thrombosis in medium size vessels leading to infarct of organs affected and severe systemic symptoms
Appears like beads on a string
Can be secondary to HBV

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8
Q

What are the symptoms of polyarteritis nodosa?

A

Skin - punched out ulcers, nodules
Renal - main cause of death - renal artery narrowing, glomerular ischaemia and HTN
Cardiac, GI and GU invovlement
Usually spares the lungs

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9
Q

How does Wergeners disease present?

A

cANCA positive
Affects the nasopharynx, lung and kidney
> rapidly progressing cresenteric glomerulonephritis
Biopsy shows inflammation and granulamas in vessel wall

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10
Q

How is Wergeners treated?

A

Corticosteriods and cyclophosphamide

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11
Q

How does Churg Strauss present?

A

pANCA - sinusitis, lung, kidney, GI, skin, nerve and heart damage
Increased eosinophils
Granulomas

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12
Q

What is the pathophysiology behind HSP?

A

IgA deposition against endothelial cells

Buttock and thigh purpura

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13
Q

Where does microscopic polyangitis affect?

A

Lungs and Kidney
pANCA positive
No granulomas

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14
Q

What is Kawaski disease?

A

Vasculitis of the coronary arteries which can lead to aneurysms and ischaemia of the coronary tissue

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15
Q

What should be done in a patient with suspected Kawaski disease?

A

MI ECHO

Aspirin and Ig IV

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16
Q

What are the features for diagnosis of Kawaski disease?

A
Conjunctivitis
Rash
Adenopathy
Strawberry tongue 
Swollen hands and feet 
Plus fever for more than five days
17
Q

What is Beurgers disease?

A

Clots in fingers and toes –> ulcer –> auto amputation

18
Q

What is GCA?

A

Inflammation of the branches of the carotid arteries. Usually the temporal artery

19
Q

How does GCA present?

A

Headaches, scalp tenderness, jaw claudication, systemic symptoms
May have vision changes including Amaurosis fugax

20
Q

What are the investigations done in GCA?

A

ESR will be greatly raised and urgent referral for biopsy

21
Q

What is the treatment for GCA?

A

Prednisolone 40mg per day
60mg if visual changes
will be on long term steriods so think about bone and GI protection

22
Q

What is affected in Takayasu arteritis?

A

Aortic arch branches - can lead to pulselessness and neuro/visual symptoms
Long term complications include limb ischaemia and renal failure

23
Q

what is the management of Takayasu disease?

A

Corticosteriods

24
Q

What are the three main features of polyarteritis nodosa?

A

Aneursym, thrombosis and infarct

25
In all vasculitis what should be done?
Urine dip to look for signs of haematuria and proteinuria
26
What may be found on examination in a patient with Takyasu?
vascular bruits may be audible over the carotids, abdominal aorta, or subclavian vessels. Unequal blood pressures may be recorded between sides, and a murmur of aortic regurgitation may be heard if there is aortic root dilation.
27
How is remission maintained in a patient with granulomatosis with polyangitis ?
Remission can be maintained using low-dose corticosteroids and either azathioprine or methotrexate.
28
6. Which is the most common type of vasculitis?
Kawasaki’s