BL- VASCULITIS Flashcards
Rheumatoid arthritis (RA) begins with inflammation in which structure/tissue?
Synovium
Clinical presentations of this type of vasculitis include temporal headache, jaw claudication, scalp tenderness, and vision loss
Giant cell arteritis
Typical histology of small vessel vasculitis:
Leukocytoclastic vasculitis
Cytoplasmic –ANCA (c-ANCA) is common to Wegener’s granulomatosis as perinuclear-ANCA (p-ANCA) is common to:
microscopic polyangiitis (MPA)
examples of immune complex (IC)-induced vasculitis
Hepatitis B-associated vasculitis
Cryoglobulinemic vasculitis
Henoch-Schönlein purpura
Hypersensitivity vasculitis (cutaneous leukocytoclastic angiitis)
suspected immunopathogenic mechanisms that mediate vasculitis
Infection of endothelial cells
Immune complexes (IC)
T cell dependent mediated endothelial cell injury
Autoantibodies such as ANCAs and antiendothelial antibodies
Immune complexes (IC)
Vasculitides are a rare group of disorders defined by the size of the vessel involved, the pathologic change in the vessel wall, and the:
clinical presentation
In primary vasculitis, the inciting agent is unknown. The vasculitic response may be due to IC deposition, autoantibodies (anti-endothelial, ANCAs), antigen-driven inflammation, and/or infection of: ______
endothelial cells
heterogeneous group of clinical disorders characterized by inflammation of blood vessels
vasculitides
Vasculitides can be primary or ____ to infectious disorders, drug hypersensitivity, connective tissue diseases, cryoglobulins, and malignancies.
secondary
Large-vessel vasculitis
Giant cell arteritis
Takayasu’s arteritis
Medium-vessel vasculitis
Polyarteritis nodosa
Kawasaki’s disease
Small-vessel vasculitis
(ANCA) positive vasculitides:
Granulomatosis with polyangiitis (Wegener’s)
Eosinophilic granulomatosis with polyangiitis
Microscopic polyangiitis (MPA
Small-vessel vasculitis
(ANCA) negative vasculitides:
Essential cryoglobulinemic vasculitis
Cutaneous leukocytoclastic angiitis
Henoch-Schönlein Purpura (HSP):
vasculitis Labs
anemia of inflammatory disease thrombocytosis low albumin elevated sed rate/crp polyclonal gammopathy