Management Strategies for Generalised Granuloma Annulare: A Systematic Review of Current and Emerging Therapies

IF 1.8 4区 医学 Q2 DERMATOLOGY
Luca Bettolini, Vincenzo Maione, Andrea Carugno, Giorgio Stabile, Antonio Podo Brunetti, Zeno Fratton, Enzo Errichetti, Nicola Zerbinati, Franco Rongioletti, Piergiacomo Calzavara-Pinton, Mariateresa Rossi, Stefano Bighetti
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Abstract

Generalised Granuloma Annulare (GGA) is a chronic inflammatory skin disorder with no standard treatment. Since the last review in 2013, new treatments and varied responses have highlighted the need for an updated synthesis to guide clinical decisions. This systematic review aimed to evaluate the epidemiology, comorbidities and treatment outcomes in patients with GGA, synthesising evidence from published studies to provide insights into both conventional and emerging therapeutic strategies. A systematic literature search was conducted in CENTRAL, Embase and PubMed, following PRISMA guidelines. Studies published in English, French or Spanish up to January 15, 2024, were included. Data extraction focused on patient demographics, comorbidities, treatment regimens and therapeutic outcomes. A total of 689 patients were included. The mean age of patients was 52.8 years, with a female predominance (72.6%). Based on this systematic review, we propose a stepwise approach: first-line treatment includes hydroxychloroquine and phototherapy (PUVA > UVA1 > nb-UVB). Oral corticosteroids along with high-potency topical steroids or calcineurin inhibitors may be used in extensive or rapidly progressive disease or as bridging therapy pending slower-acting agents. Sulfones are second-line, with oral retinoids (e.g., isotretinoin) as alternatives if contraindicated. For refractory cases, off-label anti-TNF-α agents or JAK inhibitors are recommended, with methotrexate or cyclosporine as valid alternatives. This largest systematic review of GGA treatments offers an evidence-based clinical framework. While steroids and phototherapy remain standard, emerging options like JAK inhibitors and biologics show promise for refractory cases. Tailored, multimodal strategies may improve outcomes, though further trials are needed to standardise guidelines.

Abstract Image

广泛性环形肉芽肿的管理策略:当前和新兴治疗方法的系统回顾。
广泛性肉芽肿环状(GGA)是一种慢性炎症性皮肤病,没有标准的治疗方法。自2013年的上一次审查以来,新的治疗方法和不同的反应突出了需要更新的综合来指导临床决策。本系统综述旨在评估GGA患者的流行病学、合并症和治疗结果,综合已发表研究的证据,为传统和新兴治疗策略提供见解。按照PRISMA指南,在CENTRAL、Embase和PubMed进行了系统的文献检索。截至2024年1月15日,以英语、法语或西班牙语发表的研究都被纳入其中。数据提取侧重于患者人口统计学、合并症、治疗方案和治疗结果。共纳入689例患者。患者平均年龄52.8岁,以女性为主(72.6%)。在此系统综述的基础上,我们提出了循序渐进的方法:一线治疗包括羟氯喹和光疗(PUVA > UVA1 > nb-UVB)。口服皮质类固醇与高效外用类固醇或钙调磷酸酶抑制剂可用于广泛或迅速进展的疾病,或作为桥接治疗等待缓慢作用的药物。磺胺类药物是二线药物,如果有禁忌症,可选择口服类维甲酸(如异维甲酸)。对于难治性病例,推荐使用标签外抗tnf -α药物或JAK抑制剂,甲氨蝶呤或环孢素是有效的替代品。这项针对GGA治疗的最大规模系统综述提供了一个基于证据的临床框架。虽然类固醇和光疗仍然是标准,但JAK抑制剂和生物制剂等新兴选择显示出对难治性病例的希望。量身定制的多模式策略可能会改善结果,尽管需要进一步的试验来标准化指导方针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.20
自引率
5.00%
发文量
186
审稿时长
6-12 weeks
期刊介绍: Australasian Journal of Dermatology is the official journal of the Australasian College of Dermatologists and the New Zealand Dermatological Society, publishing peer-reviewed, original research articles, reviews and case reports dealing with all aspects of clinical practice and research in dermatology. Clinical presentations, medical and physical therapies and investigations, including dermatopathology and mycology, are covered. Short articles may be published under the headings ‘Signs, Syndromes and Diagnoses’, ‘Dermatopathology Presentation’, ‘Vignettes in Contact Dermatology’, ‘Surgery Corner’ or ‘Letters to the Editor’.
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