Albers Lauren N, Arbiser Jack L, Feldman Ron J
Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia.
Atlanta Veterans Administration Medical Center, Decatur, Georgia.
JAMA Dermatol. 2017 Oct 1;153(10):1018-1020. doi: 10.1001/jamadermatol.2017.2446.
Hailey-Hailey disease is a severe genetic blistering disease of intertriginous skin locations that can lead to poor quality of life and increased morbidities. Multiple therapies are available with inconsistent outcomes and potentially severe adverse effects.
To determine whether low-dose naltrexone is an effective treatment for Hailey-Hailey disease.
DESIGN, SETTING, AND PARTICIPANTS: This study was a case series performed at a dermatology outpatient clinic of 3 patients with severe Hailey-Hailey disease recalcitrant to at least 4 therapies.
Low-dose naltrexone, 3 mg nightly, titrated to 4.5 mg nightly in 2 patients.
Reduction in size of lesions as well as subjective improvement of symptoms.
All 3 patients noted significant healing of erosions and plaques starting from the peripheral aspect within 1 to 2 weeks of treatment, and clinical resolution of lesions within 2 months. Discontinuation of low-dose naltrexone resulted in flaring of symptoms, which cleared within 2 to 3 days on rechallenge with low-dose naltrexone.
We present herein 3 cases of patients with severe Hailey-Hailey disease treated with low-dose naltrexone who achieved clinical resolution of symptoms. The success of these cases suggests low-dose naltrexone as a novel therapy for Hailey-Hailey disease. The possible mechanism may involve low-dose naltrexone influencing opioid or toll-like receptor signaling to improve calcium mobilization and improve keratinocyte differentiation and wound healing. Future studies are needed to clarify the mechanism and to define the role of low-dose naltrexone for treatment of Hailey-Hailey disease.
黑利-黑利病是一种发生于皮肤褶皱部位的严重遗传性水疱病,可导致生活质量下降和发病率增加。有多种治疗方法,但疗效不一,且可能有严重不良反应。
确定低剂量纳曲酮是否为治疗黑利-黑利病的有效方法。
设计、地点和参与者:本研究为病例系列研究,在一家皮肤科门诊对3例重度黑利-黑利病患者进行,这些患者对至少4种治疗方法均无效。
低剂量纳曲酮,每晚3毫克,2例患者逐渐滴定至每晚4.5毫克。
皮损大小减小以及症状主观改善。
所有3例患者均指出,治疗1至2周内从皮损周边开始糜烂和斑块显著愈合,2个月内皮损临床消退。停用低剂量纳曲酮导致症状复发,再次使用低剂量纳曲酮后2至3天症状缓解。
我们在此报告3例重度黑利-黑利病患者接受低剂量纳曲酮治疗后症状获得临床缓解的病例。这些病例的成功表明低剂量纳曲酮可作为黑利-黑利病的一种新疗法。可能的机制可能是低剂量纳曲酮影响阿片类或Toll样受体信号传导,以改善钙动员并促进角质形成细胞分化和伤口愈合。需要进一步研究以阐明其机制,并明确低剂量纳曲酮在黑利-黑利病治疗中的作用。