Literature DB >> 8543412

Idiopathic hypersensitivity vasculitis: clinicopathologic correlation of 61 cases.

K V Ratnam1, Y H Boon, B K Pang.   

Abstract

BACKGROUND: Little is known of the course and prognosis of hypersensitivity vasculitis (HV).
METHODS: Sixty-one cases of idiopathic HV were biopsied and followed-up for 5 years.
RESULTS: There were two predominant patterns of presentation: palpable purpura (PP) and vasculitic ulcers (VU). The former was self-limiting, whereas the prognosis of the latter was poor. Findings on histopathology correlate well in PP patients having acute episodes, whereas in patients with VU there is correlation with duration and recurrence.
CONCLUSION: A biopsy of a fresh lesion is recommended to help in determining the outcome.

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Year:  1995        PMID: 8543412     DOI: 10.1111/j.1365-4362.1995.tb04398.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  3 in total

1.  Orbital inflammatory pseudotumor due to hypersensitivity vasculitis and mononeuritis multiplex in a patient with atypical, cANCA-positive Wegener's granulomatosis.

Authors:  Jörg Kaufmann; Eberhard Schulze; Ulrich Voigt; Jürgen Strobel; Gert Hein; Günter Stein
Journal:  Rheumatol Int       Date:  2003-04-17       Impact factor: 2.631

2.  Severe leukocytoclastic vasculitis secondary to the use of a naproxen and requiring amputation: a case report.

Authors:  Keri Brown; Jeanine Martin; Susan Zito
Journal:  J Med Case Rep       Date:  2010-07-01

3.  A Cross-Sectional Study to Correlate Serum Complement C3 and C4 Levels With Clinical and Pathological Severity in Cutaneous Small-Vessel Vasculitis.

Authors:  Namrata Sarkar; Aparna Palit; Madhusmita Sethy; Biswanath Behera; Siddhartha Dash; Dinesh P Sahu
Journal:  Cureus       Date:  2022-05-09
  3 in total

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