Patterson R, Wong S, Dykewicz M S, Harris K E
Department of Medicine, Northwestern University Medical School, Chicago, Ill 60611.
J Allergy Clin Immunol. 1990 Jan;85(1 Pt 1):86-8. doi: 10.1016/0091-6749(90)90226-t.
A patient with idiopathic anaphylaxis (IA), classified as generalized IA with frequent episodes, had original episodes in 1985 and has been managed and studied by the authors since 1987. Although her episodes of IA appear to have been controlled by prednisone, progressively larger doses of prednisone have been required. The patient was classified as a patient with corticosteroid-dependent IA, a subset of patients with IA in whom a remission cannot be induced with prednisone and in whom prednisone cannot be stopped. A trial of ketotifen is in progress without definitive effect on prednisone requirement. Because this corticosteroid-dependent patient with IA, which is potentially fatal, cannot be managed on less than 90 mg of alternate-day prednisone, we propose the term malignant IA to categorize such severe cases of IA.
一名特发性过敏反应(IA)患者,被归类为发作频繁的全身性IA,于1985年首次发作,自1987年以来一直由作者进行管理和研究。尽管她的IA发作似乎已被泼尼松控制,但所需泼尼松的剂量却越来越大。该患者被归类为依赖皮质类固醇的IA患者,这是IA患者中的一个亚组,在该亚组中,泼尼松无法诱导缓解,也无法停用泼尼松。目前正在进行酮替芬试验,但对泼尼松的需求量没有明确影响。由于这名依赖皮质类固醇的IA患者有潜在致命风险,且隔日服用少于90毫克泼尼松时病情无法得到控制,我们建议用“恶性IA”这一术语来对这类严重的IA病例进行分类。