List 4 types of vasculitis which affect the small sized vessels
List 3 types of vasculitis which affect the medium sized vessels
List 2 types of vasculitis which affect the large sized vessels
List 4 features of a vasculitis
List 4 systemic manifestations of vasculitis
Specific test findings for vasculitis
Compare pANCA vs cANCA
p-ANCA (MPO antibodies): Microscopic polyangiitis and Churg-Strauss syndrome
c-ANCA (PR3 antibodies): Wegener’s granulomatosis
What is Henoch-Schonlein Purpura?
An IgA vasculitis that commonly presents with a purpuric rash affecting the lower limbs or buttocks in children (< 10 yrs)
Most common cause of HSP?
Often triggered by an upper airway infection (e.g. tonsillitis) or a gastroenteritis
Four classic features of HSP?
Management of HSP
Supportive ie. simple analgesia, rest and proper hydration
How does Eosinophilic granulomatosis with polyangiitis commonly present?
(Churg-Strauss syndrome)
Presents with severe asthma in late teenage years or adulthood
Most associated with lung and skin problems
Characteristic finding on FBC of Churg-Strauss syndrome
↑ eosinophil levels
Main feature of Microscopic polyangiitis
Renal failure
(can also affect the lungs causing SOB and haemoptysis)
Classic presentation/features of Wegener’s granulomatosis?
(Granulomatosis with polyangiitis)
What is Polyarteritis Nodosa?
Medium vessel vasculitis associated with hepatitis B
Associated with a rash called livedo reticularis. - mottled, purplish, lace like rash
What is Kawasaki Disease
Medium vessel vasculitis which affects young children (< 5) with no clear cause
Clinical features of Kawasaki Disease
Key complication of Kawasaki Disease
coronary artery aneurysms
Treatment of Kawasaki Disease
Aspirin and IV immunoglobulins
What is Takayasu’s arteritis?
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”
How does Takayasu’s arteritis?
How does Takayasu’s arteritis present?
Before 40 years with:
How is Takayasu’s arteritis diagnosed