Department of Dermatology, Rabin Medical Center, Petach Tikva, Israel.
Dermatology. 2013;227(1):37-44. doi: 10.1159/000351559. Epub 2013 Aug 31.
BACKGROUND/OBJECTIVE: Alopecia areata may occur at any age, though usually before the age of 20 years. Treatment often consists of systemic steroids administered as high-dose bolus infusions. This study sought to investigate the effectiveness and side effects of intravenous high-dose pulse corticosteroids in children with alopecia areata and to identify prognostic factors for successful treatment.
Patients treated with pulse corticosteroids for alopecia areata in 2001-2008 at the day care unit of a tertiary pediatric medical center were identified by computerized file search and clinical treatment and outcome data were collected.
The sample included 24 children (16 female, 8 male) with a mean age of 8.5 ± 4.6 years at diagnosis; 8 (33%) had multifocal disease,10 (42%) multifocal disease with ophiasis, 4 (17%) alopecia totalis and 2 (8%) alopecia universalis. Nail involvement was noted in 9 patients (38%). Mean duration of disease was 22 ± 27 months. Patients were treated with 8 mg/kg body weight intravenous methylprednisolone on 3 consecutive days at 1-month intervals. After a mean of 5.65 ± 1.95 courses, 9 patients (38%) had a complete response, 7 (29%) a partial response and 8 (33%) no response. Of the 16 responders, 13 (81%) relapsed at 9.5 ± 12 months after the last course; 3 patients had side effects, none of which were severe. Three positive prognostic factors were identified: short disease duration (≤6 months), younger age at disease onset (<10 years) and multifocal disease (as opposed to severe, diffuse variants).
Careful patient selection is necessary to achieve maximal benefit from pulse corticosteroid treatment for alopecia areata in children.
背景/目的:斑秃可发生于任何年龄,但通常发生在 20 岁之前。治疗通常包括全身皮质类固醇激素治疗,如大剂量冲击疗法。本研究旨在探讨静脉内大剂量脉冲皮质类固醇激素治疗儿童斑秃的有效性和副作用,并确定治疗成功的预测因素。
通过计算机文件检索和临床治疗及转归数据收集,确定了 2001-2008 年在一家三级儿科医疗中心日间病房接受脉冲皮质类固醇激素治疗的斑秃患儿。
该样本包括 24 例儿童(16 例女性,8 例男性),诊断时的平均年龄为 8.5 ± 4.6 岁;8 例(33%)为多灶性疾病,10 例(42%)为多灶性疾病伴脱发,4 例(17%)为全秃,2 例(8%)为普秃。9 例(38%)患者有指甲受累。疾病的平均持续时间为 22 ± 27 个月。患者在 1 个月的间隔内接受 3 天 8mg/kg 体重的静脉内甲基泼尼松龙治疗。在平均 5.65 ± 1.95 个疗程后,9 例(38%)患者完全缓解,7 例(29%)部分缓解,8 例(33%)无反应。在 16 例缓解者中,13 例(81%)在最后一次治疗后 9.5 ± 12 个月复发;3 例患者出现副作用,但均不严重。确定了 3 个阳性预后因素:疾病病程短(≤6 个月)、发病年龄较小(<10 岁)和多灶性疾病(与严重、弥漫性病变相反)。
为了从儿童斑秃的脉冲皮质类固醇激素治疗中获得最大益处,需要对患者进行仔细选择。