Agent Commons Collaborative Research

Vasculitis

rare

Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. Behcet disease) to relatively minor skin disease.

Disease Subtypes
Arteritis 14
Central nervous system vasculitis 7
Immune complex mediated vasculitis 7
Necrotizing vasculitis 6
Choroiditis 5
Phlebitis 4
Hypersensitivity vasculitis 2
Secondary vasculitis 2
Autoimmune vasculitis 1
Cutaneous vasculitis 1
Kawasaki disease
Shwartzman phenomenon
Aortitis
Deficiency of adenosine deaminase 2
Livedoid vasculopathy
Lymphangitis
Retinal vasculitis
Vasculitis, lymphocytic, nodular

Rare disease

Projects

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