3.1.4 Vasculitis Disorders Flashcards
What is Churg-Strauss Syndrome?
Systemic vasculitis associated with prominent eosinophilia that occurs in young persons with astham or allergy
What is this?
Fibrinoid necrosis associated with polyarteritis nodosa
What is this an image of?
Polyarteritis nodosa
What is this an image of?
Microscopic Polyangiitis
What are the pathological indications of giant cell arteritis?
Multinucleated giant cells
Cordlike, nodular vessel with narrow lumen
Fibrous media and thickened intima
In giant cell arteritis what are each of the images?
The image on the left in showing granulmonas while the image on the right is showing mixed inflammation with necrosis
Takayasu arteritis is also known as what?
The pulseless disease
What is Wegner Granulomatosis?
Systemic necrotizing granulomatous vasculitis of unknown etiology.
What are the pathological findings associated with thromboangiitis obliterans?
Thrombosis and infarcts. Gangrene.
What are the pathological characteristic of polyarteritis nodosa?
Affecting small to medium vessels. Fibrinoid necrosis. Thrombosis and infarction of an organ
How do you treat Takayasu arteritis?
Steroids and surgical reconstruction
How would you treat Giant cell arteritis?
Steroids and anti-TNF
What is this an image of?
Giant cell arteritis
What would the gross and pathological finding be in a person with microscopic polyangiitis?
Localized cutaneous vasculitis - Gross
Patho - finrinoid necrosis, acute inflammation, and extravasation of RBCs
What are the hallmark characteristic of giant cell ateritis?
Also known as Temporal, Granulomatous Ateritis. It is the most common form of vasculitis. Focal, chronic, granulomatous inflammation of the temporal artery. Multinucleated giant cells
How would you treat Churg-Strauss Syndrome?
STEROIDS
What are the clinical features of Takayasu arteritis?
Weak or non-existant pulse
high BP
Ocular disturbances
syncope and dizziness