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本文引用的文献

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Management of familial benign chronic pemphigus.家族性良性慢性天疱疮的治疗
Clin Cosmet Investig Dermatol. 2016 Sep 14;9:281-290. doi: 10.2147/CCID.S89483. eCollection 2016.
2
Efficacy of magnesium chloride in the treatment of Hailey-Hailey disease: from serendipity to evidence of its effect on intracellular Ca(2+) homeostasis.氯化镁治疗黑利-黑利病的疗效:从偶然发现到其对细胞内Ca(2+) 稳态影响的证据
Int J Dermatol. 2015;54(5):543-8. doi: 10.1111/ijd.12410. Epub 2014 Nov 28.
3
Activation of the δ-opioid receptor promotes cutaneous wound healing by affecting keratinocyte intercellular adhesion and migration.δ-阿片受体的激活通过影响角质形成细胞的细胞间黏附和迁移来促进皮肤伤口愈合。
Br J Pharmacol. 2015 Jan;172(2):501-14. doi: 10.1111/bph.12687. Epub 2014 Jul 1.
4
Low dose naltrexone for induction of remission in Crohn's disease.低剂量纳曲酮诱导克罗恩病缓解
Cochrane Database Syst Rev. 2014 Feb 21(2):CD010410. doi: 10.1002/14651858.CD010410.pub2.
5
The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain.低剂量纳曲酮(LDN)作为慢性疼痛新型抗炎治疗方法的应用。
Clin Rheumatol. 2014 Apr;33(4):451-9. doi: 10.1007/s10067-014-2517-2. Epub 2014 Feb 15.
6
Human keratinocytes express functional CD14 and toll-like receptor 4.人角质形成细胞表达功能性CD14和Toll样受体4。
J Invest Dermatol. 2002 Aug;119(2):424-32. doi: 10.1046/j.1523-1747.2002.01847.x.
7
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease.编码一种钙泵的ATP2C1基因发生突变会导致黑利-黑利病。
Nat Genet. 2000 Jan;24(1):61-5. doi: 10.1038/71701.

低剂量纳曲酮治疗黑利-黑利病

Treatment of Hailey-Hailey Disease With Low-Dose Naltrexone.

作者信息

Albers Lauren N, Arbiser Jack L, Feldman Ron J

机构信息

Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia.

Atlanta Veterans Administration Medical Center, Decatur, Georgia.

出版信息

JAMA Dermatol. 2017 Oct 1;153(10):1018-1020. doi: 10.1001/jamadermatol.2017.2446.

DOI:10.1001/jamadermatol.2017.2446
PMID:28768313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5817589/
Abstract

IMPORTANCE

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.

OBJECTIVE

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.

INTERVENTIONS

Low-dose naltrexone, 3 mg nightly, titrated to 4.5 mg nightly in 2 patients.

MAIN OUTCOMES AND MEASURES

Reduction in size of lesions as well as subjective improvement of symptoms.

RESULTS

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.

CONCLUSIONS AND RELEVANCE

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.

摘要

重要性

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。

目的

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。

干预措施

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。

主要结局和衡量指标

皮损大小减小以及症状主观改善。

结果

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。

结论和相关性

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。