Immunoglobulin A vasculitis (IgAV), also referred to as Henoch-Schönlein purpura, is the
most common form of childhood vasculitis. The pathogenesis of IgAV is still largely …

Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the
most common systemic vasculitis in children, characterized by diverse clinical …

Giant cell arteritis (GCA) is a granulomatous vasculitis affecting large arteries, especially the
aorta and the extracranial branches of the external carotid artery. Its exact pathogenesis is …

Susac syndrome is a disorder thought to be mediated by an autoimmune response towards
endothelial cells, leading to a characteristic clinical triad of encephalopathy, visual …

Autoimmune and autoinflammatory diseases of the medium and large arteries, including the
aorta, cause life-threatening complications due to vessel wall destruction but also by wall …

Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease with a
complex pathogenesis. Neuropsychiatric systemic lupus erythematosus (NPSLE) is a …

The exact classification of Kawasaki disease (KD) has been debated. Infectious disease
specialists have claimed it as an infection with a classic immune responses to an as yet …

The term “vasculitis” refers to a group of rare immune‐mediated diseases characterized by
the dysregulated immune system attacking blood vessels located in any organ of the body …

Thromboangiitis obliterans (TAO) or Buerger's disease is a segmental inflammatory,
thrombotic occlusive peripheral vascular disease with unknown aetiology that usually …

The clinical features of the kidney involvement in immunoglobulin A (IgA) vasculitis (IgAVN)
differ in children and adults for both clinical presentation and progression. IgAVN in children …