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Updated: May 8, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
[ANCA associated vasculitis]
Monika Ryba1, Zbigniew Hruby, Wojciech Witkiewicz
1Wrovasc--Zintegrowane Centrum Medycyny, Sercowo-Naczyniowej, Wojewódzki Szpital Specjalistyczny we Wrocławiu, Ośrodek Badawczo-Rozwojowy.
Insights
Small-vessel vasculitis involves inflammation of small blood vessels, often linked to antineutrophil cytoplasm antibodies (ANCA). This condition, increasingly seen in the elderly, affects organs like the lungs, kidneys, and skin, requiring treatments such as corticosteroids and immunosuppressants.
Area of Science:
- Rheumatology
- Immunology
- Nephrology
Background:
- Vasculitis encompasses diverse disorders characterized by blood vessel wall inflammation and necrosis.
- Classification is based on vessel size: large-, medium-, or small-vessel vasculitis.
- Small-vessel vasculitis affects arterioles, venules, and capillaries, sometimes involving medium arteries.
Purpose of the Study:
- To provide an overview of small-vessel vasculitis.
- To highlight key associated conditions and clinical manifestations.
- To briefly touch upon current treatment strategies.
Main Methods:
- Review of existing literature on vasculitis classification and small-vessel vasculitis.
- Identification of common small-vessel vasculitis types, including Granulomatosis with polyangiitis, Microscopic polyangiitis, Churg Strauss syndrome, and Renal Limited Vasculitis.
- Summary of typical clinical presentations and diagnostic associations, such as antineutrophil cytoplasm antibodies (ANCA).
Main Results:
- Small-vessel vasculitis includes conditions like Granulomatosis with polyangiitis and Microscopic polyangiitis.
- These disorders are frequently associated with ANCA and are increasingly diagnosed in the elderly.
- Manifestations include alveolar hemorrhage (lungs), glomerulonephritis (kidneys), and purpuric rash (skin).
Conclusions:
- Small-vessel vasculitis presents with focal necrotizing lesions affecting multiple organs.
- Treatment typically involves corticosteroids, immunosuppressants, and sometimes plasmapheresis.
- Recent advancements have improved clinical management of these conditions.
Abstract:
Vasculitis is a process caused by inflammation and necrosis of blood vessel walls and results in a variety of disorders. An accepted classification system for vasculitis is categorized by the size or type of the involved blood vessel as large-, medium-, or small-vessel vasculitis. Small-vessel vasculitis is defined as vasculitis that affects vessels smaller than arteries (i.e., arterioles, venules, and capillaries); however, small-vessel vasculitis can also involve medium-sized arteries. Granulomatosis with polyangiitis, Microscopoc polyangiitis, Churg Strauss syndrome and Renal Limited Vasculitis where the kidney is the only organ involved are clasified as a small vesselvasculitis. These disorders are described to be commonly associated with antineutrophil cytoplasm antibodies (ANCA). The etiology is not known and the incidence of vasculitis is incresasing occuring more often in elderly population. These diseases can cause the focal necrotizing lesions witch affect vessels and organs. In the lung it may cause alveolar hemorrhage, in the kidneys crescentic glomerulonephritis with acute renal failure, in the skin purpuric rash and ulcerations. Treatment usually includes corticosteroids, immunosupresive therapy and in some cases plasmapheresis. Advances in clinical management have been achieved during the past few years.
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