TY - JOUR
T1 - Small-vessel vasculitis
AU - Iglesias-Gamarra, Antonio
AU - Restrepo, José Félix
AU - Matteson, Eric L.
N1 - Funding Information:
He has received grant support from Amgen, Genentech, the Mayo Foundation for Medical Education and Research (Rochester, MN), Novartis International AG (Basel, Switzerland), and the US National Institutes of Health. In addition, Dr. Matteson has served as a consultant to Biogen Idec, Centocor Inc., Endocyte Inc., Novartis, SGS US Testing Company (Fairfield, NJ) and Watermark Research Partners (Cincinnati, OH) and on the Scientific Advisory Board of The Vasculitis Foundation (Kansas City, MO).
PY - 2007/8
Y1 - 2007/8
N2 - Small-vessel vasculitis is a convenient descriptor for a wide range of diseases characterized by vascular inflammation of the venules, capillaries, and/or arterioles with pleomorphic clinical manifestations. The classical clinical phenotype is leukocytoclastic vasculitis with palpable purpura, but manifestations vary widely depending upon the organs involved. Histopathologic examination in leukocytoclastic vasculitis reveals angiocentric segmental inflammation, fibrinoid necrosis, and a neutrophilic infiltrate around the blood vessel walls with erythrocyte extravasation. The etiology of small-vessel vasculitis is unknown in many cases, but in others, drugs, post viral syndromes, malignancy, primary vasculitis such as microscopic polyarteritis, and connective tissue disorders are associated. The diagnosis of small-vessel vasculitis relies on a thorough history and physical examination, as well as relevant antibody testing including antinuclear antibody and antineutrophil cytoplasmic antibody, hepatitis B and C serologies, assessment of complement, immunoglobulins, blood count, serum creatinine, liver function tests, urinalysis, radiographic imaging, and biopsy.
AB - Small-vessel vasculitis is a convenient descriptor for a wide range of diseases characterized by vascular inflammation of the venules, capillaries, and/or arterioles with pleomorphic clinical manifestations. The classical clinical phenotype is leukocytoclastic vasculitis with palpable purpura, but manifestations vary widely depending upon the organs involved. Histopathologic examination in leukocytoclastic vasculitis reveals angiocentric segmental inflammation, fibrinoid necrosis, and a neutrophilic infiltrate around the blood vessel walls with erythrocyte extravasation. The etiology of small-vessel vasculitis is unknown in many cases, but in others, drugs, post viral syndromes, malignancy, primary vasculitis such as microscopic polyarteritis, and connective tissue disorders are associated. The diagnosis of small-vessel vasculitis relies on a thorough history and physical examination, as well as relevant antibody testing including antinuclear antibody and antineutrophil cytoplasmic antibody, hepatitis B and C serologies, assessment of complement, immunoglobulins, blood count, serum creatinine, liver function tests, urinalysis, radiographic imaging, and biopsy.
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U2 - 10.1007/s11926-007-0049-3
DO - 10.1007/s11926-007-0049-3
M3 - Review article
C2 - 17688840
AN - SCOPUS:34547924489
SN - 1523-3774
VL - 9
SP - 304
EP - 311
JO - Current Rheumatology Reports
JF - Current Rheumatology Reports
IS - 4
ER -