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[对H1抗组胺药耐药的慢性荨麻疹的治疗]

[Treatment of chronic urticaria resistant to H1 antihistamines].

作者信息

Guinnepain M-T

机构信息

Service d'Allergologie Clinique, Institut Pasteur, 28, rue du Docteur Roux, 75015 Paris.

出版信息

Ann Dermatol Venereol. 2003 May;130 Spec No 1:1S78-85.

Abstract

Urticaria is a syndrome. Several signalisation factors (cytokines and chemokines) are implicated in activation of mast cells receptors. Immunologic or non immunologic mechanisms elicit mediator releases and inflammatory activities inducing urticaria lesions. In chronic urticaria the removal of an hypothetical cause is not possible, and the therapeutic management is first oriented towards palliation of symptoms. H1 antagonists are the treatment of choice. Higher dosage than those recommended may be necessary. But severely affected patients are not enough improved. Triggering factors should be avoided. Addition of other mediator antagonists such as leukotriene receptor antagonists have improved some patients and need further evaluation. Several alternative pathogenic therapies have been proposed with conflicting results. Tolerance induction may be tried in a few cases of severe physical urticaria. Oral steroids are reserved if possible for systemic urticaria and in short course for severe exacerbation. Immunosuppressive agents are only appropriate for patients with refractory urticaria to classical treatment. Oral cyclosporine has been used with encouraging results. Its has a suspensive effect but relapses can be treated by H1 antagonists. Whichever the drug or association of drug individual variations in the course of the disease need periodic reevaluation. A spontaneous unexplained remission is not an exception. In this heterogeneous disease an individual approach is required, leading to reduction of symptoms with the least invasive therapy, carefully balancing risk and benefits.

摘要

荨麻疹是一种综合征。多种信号传导因子(细胞因子和趋化因子)参与肥大细胞受体的激活。免疫或非免疫机制引发介质释放和炎症活动,从而导致荨麻疹皮损。在慢性荨麻疹中,无法去除假定的病因,治疗管理首先着眼于症状的缓解。H1拮抗剂是首选治疗药物。可能需要高于推荐剂量的药物。但严重患者的病情改善不足。应避免诱发因素。添加其他介质拮抗剂,如白三烯受体拮抗剂,已使部分患者病情改善,尚需进一步评估。已提出多种替代致病疗法,但结果相互矛盾。在少数严重物理性荨麻疹病例中可尝试诱导耐受。口服类固醇尽可能仅用于全身性荨麻疹,且仅在严重病情加重时短期使用。免疫抑制剂仅适用于对传统治疗难治的荨麻疹患者。口服环孢素已取得令人鼓舞的效果。它有缓解作用,但复发时可用H1拮抗剂治疗。无论使用何种药物或药物组合,疾病过程中的个体差异都需要定期重新评估。自发的不明原因缓解并不罕见。在这种异质性疾病中,需要采取个体化方法,以侵入性最小的治疗减轻症状,仔细权衡风险和益处。

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