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特发性日光性荨麻疹的特征与预后:87例队列研究

Characteristics and prognosis of idiopathic solar urticaria: a cohort of 87 cases.

作者信息

Beattie Paula E, Dawe Robert S, Ibbotson Sally H, Ferguson James

机构信息

Photobiology Unit, Ninewells Hospital and Medical School, Dundee, Scotland.

出版信息

Arch Dermatol. 2003 Sep;139(9):1149-54. doi: 10.1001/archderm.139.9.1149.

Abstract

BACKGROUND

As little has been published on the course of idiopathic solar urticaria (SU) patients cannot receive comprehensive prognostic advice.

OBJECTIVE

To determine the prognosis and photobiological characteristics of idiopathic SU.

DESIGN

Historical cohort study, with inception cohort followed up from time of diagnosis. Follow-up for a median of 4 years (range, 3 months to 26 years) after diagnosis.

SETTING

Tertiary referral center for the investigation of photodermatoses in Scotland.

PATIENTS

The study included 87 patients, 61 (70%) of whom were female, with phototest-confirmed idiopathic SU between 1975 and 2000. Sixty patients (69%) were followed up clinically, and 25 patients (29%) were phototested on 2 or more occasions.

INTERVENTIONS

Investigations at time of diagnosis included monochromator phototesting. Further monochromator phototesting was performed in those patients in whom it was clinically indicated (select subgroup), and all patients who could be traced received a follow-up questionnaire.

MAIN OUTCOME MEASURES

Characteristics of SU, responsible wave bands, and prognosis for clinical resolution.

RESULTS

The prevalence of idiopathic SU in Tayside, Scotland, is estimated to be 3.1 per 100 000. Action spectra were typically broad, with 63% reacting to more than 1 wave band, and the most common provoking wavelengths were the longer UV-A and the shorter visible ones. The majority of subjects were affected perennially (68%), by radiation transmitted through glass (83%) and thin clothing (76%). Coexistent polymorphic light eruption occurred in 20 patients (23%), and another photodermatosis occurred in 6 patients, 3 of whom had chronic actinic dermatitis. In those with SU alone, the mean age at onset was 41 years. The probability of clinical resolution at 5 and 10 years after diagnosis was 0.12 (95% confidence interval, 0.06-0.24) and 0.26 (95% confidence interval, 0.15-0.43), respectively.

CONCLUSION

Idiopathic SU is a chronic disease. The majority of this cohort was still affected after 5 and 10 years.

摘要

背景

由于关于特发性日光性荨麻疹(SU)病程的报道较少,患者无法获得全面的预后建议。

目的

确定特发性SU的预后及光生物学特征。

设计

历史性队列研究,自诊断时起对起始队列进行随访。诊断后中位随访4年(范围3个月至26年)。

地点

苏格兰光皮肤病研究的三级转诊中心。

患者

本研究纳入了87例患者,其中61例(70%)为女性,于1975年至2000年间经光试验确诊为特发性SU。60例患者(69%)接受了临床随访,25例患者(29%)接受了2次或更多次光试验。

干预措施

诊断时的检查包括单色仪光试验。对临床有指征的患者(选定亚组)进行进一步的单色仪光试验,所有可追踪到的患者均收到一份随访问卷。

主要观察指标

SU的特征、致病波段及临床缓解的预后。

结果

据估计,苏格兰泰赛德地区特发性SU的患病率为每10万人中有3.1例。作用光谱通常较宽,63%的患者对不止一个波段有反应,最常见的激发波长是较长的UV - A和较短的可见光波长。大多数患者常年发病(68%),受透过玻璃(83%)和薄衣物(76%)传播的辐射影响。20例患者(23%)并发多形性日光疹,6例患者并发另一种光皮肤病,其中3例患有慢性光化性皮炎。仅患SU的患者发病时的平均年龄为41岁。诊断后5年和10年临床缓解的概率分别为0.12(95%置信区间,0.06 - 0.24)和0.26(95%置信区间,0.15 - 0.43)。

结论

特发性SU是一种慢性疾病。该队列中的大多数患者在5年和10年后仍受影响。

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