Vasculitis Flashcards

1
Q

Name subtypes of large vessel vasculitis

A

Giant cell arteritis
Takayaso

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2
Q

Name subtypes of medium vessel vasculitis

A

PAN
Kawasaki

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3
Q

Name types of Small/ Medium vessel vasculitis:

A

• Wegener’s granulomatosis
• Churg-Strauss syndrome
• Microscopic polyangiitis

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4
Q

Name subtypes of small vessel vasculitis

A

*Henoch Schonlein Purpura
• Essential mixed cryoglobulinaemia

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5
Q

Management of polymyalgia rheumatica

A

– Prednisolone 15 mg od
– Bone protection (bisphosphonate, Calcium and vitamin D)
– GI protection (e.g. PPI)

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6
Q

Management of GIANT cell arteritis

A

Prednisolone 40-80 mg od
• 40 mg if no visual/ocular symptoms
• 60-80 (1mg/kg) if suspect visual/ocular involvement
– Bone protection (bisphosphonate, Calcium and vitamin D)
– GI protection (e.g. PPI)

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7
Q

Management of Takayaso arteritis

A

Prednisolone +/- steroid sparing agents
– Monitor and treat cardiovascular risk factors
– Surgery – reconstructive/angioplasty

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8
Q

Pt comes with
. Claudication of extremities
. Decreased pulsations of one or two limbs
. Difference of 10 mmhg in systolic pressure betwen both arms
. Bruit ober the subclavian arteries

Diagnosis?

A

Takayaso’s arteritis

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9
Q

Pt. Comes with
Triad of systemic necrotising vasculitis affecting
• Upper airway (ENT)
• Lung
• Kidney
– cANCA (anti-PR3) positive

Diagnosis

A

Wegener’s granulomatosis

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10
Q

Pt comes with Triad of
Asthma
• Eosinophilia
• Systemic vasculitis involving >2 extrapulmonary organs

Diagnosis?

A

Churg Strauss Syndrome
(Eosinophilic Granulomatosis with Polyangiitis (EGPA)

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11
Q

Pt comes with Symmetrical purpura
• GI – colic, maelena, haematemesis
• Joints – arthritis/arthralgia
• Renal – haematuria, proteinuria

He recently recovered from upper resp. Infection

Diagnosis?

A

HSP

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12
Q

Management of HSP

A

Usually self-limiting
– Supportive
– Corticosteroid, immunosuppressants, plasma exchange in severe

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13
Q

Patient comes with – Palpable purpura (esp exposed areas, extremities)
– Arthritis/arthralgia
– Weakness
– Peripheral neuropahty
– Subclinical alveolitis
– Low C4

Diagnosis?

A

Essential mixed cryoglobulinaemia
Cryoglobulinemic Vasculitis

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14
Q

Management of essential mixed cryoglobulinaemia

A

Immunosuppression
• Plasma exchange

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