Abstract |
Hypersensitivity vasculitis (HSV) is characterized by palpable purpura and arthralgia, the existence of precipitating factors(medications or infections), and leukocytoclastic vasculitis in the skin lesion. It is known by a variety of names, including leukocytoclastic vasculitis, cutaneous small-vessel vasculitis (CSVV), allergic vasculitis. Patients are classified as HSV according to the criteria proposed by a subcommittee of the American College of Rheumatology (ACR) in 1990. HSV is distinguished from Henoch-Schönlein purpura that has a higher risk of gastrointestinal and renal involvement. Systemic involvement in HSV is rare and its prognosis is excellent. Most cases in HSV are self-limited if the precipitant can be removed.
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Authors | Hiroko Nagafuchi, Hidehiro Yamada |
Journal | Nihon rinsho. Japanese journal of clinical medicine
(Nihon Rinsho)
Vol. 67
Issue 11
Pg. 2148-51
(Nov 2009)
ISSN: 0047-1852 [Print] Japan |
PMID | 19899532
(Publication Type: English Abstract, Journal Article, Review)
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Topics |
- Humans
- Vasculitis, Leukocytoclastic, Cutaneous
(diagnosis, drug therapy)
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