Tissue eosinophilia as an indicator of drug-induced cutaneous small-vessel vasculitis

被引:56
作者
Bahrami, S
Malone, JC
Webb, KG
Callen, JP
机构
[1] Univ Louisville, Sch Med, Dept Internal Med, Div Dermatol, Louisville, KY 40292 USA
[2] Univ Louisville, Sch Med, Dept Pathol, Louisville, KY 40292 USA
关键词
D O I
10.1001/archderm.142.2.155
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: To determine whether tissue eosinophilia is a reliable indicator of a drug-induced etiology in biopsy samples demonstrating leukocytoclastic vasculitis. Design: Retrospective medical record review with concurrent histopathologic analysis. Setting: University-affiliated dermatology practice. Patients: Sixty-three patients with cutaneous small-vessel vasculitis meeting specific inclusion criteria were divided into drug-induced (n = 16) and non - drug-induced (n = 47) groups. Main Outcome Measures: Corresponding histopathologic material was reviewed by a dermatopathologist masked to the etiologic associations. An eosinophil ratio was calculated for each patient, derived from the mean eosinophil score ( averaging eosinophil counts from 10 high-power histologic fields), and expressed in relation to the intensity of inflammation in the histopathologic slides examined. Eosinophilia ratios were compared for both groups using the Mann-Whitney test. Results: A significant difference was found in mean eosinophil ratios in the drug-induced vs non - drug-induced groups (5.20 vs 1.05; P =. 01). Vascular fibrin deposition was present in both groups and was not found to be significantly different (P =. 78). Clinical evidence of systemic vasculitis was present in 2 patients (13%) in the drug-induced group vs 15 (32%) in the non - drug-induced group. Fourteen patients (88%) in the drug-induced group had a short-term disease course vs 27 (57%) in the non - drug-induced group. Conclusions: Tissue eosinophilia is established as a reliable indicator of drug induction in cutaneous small vessel vasculitis. Drug-induced small-vessel vasculitis generally follows a short-term disease course without development of systemic involvement. This information may be useful for guiding management decisions, especially when the etiology is unclear.
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页码:155 / 161
页数:7
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