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《Sturge-Weber 综合征中葡萄酒色斑的管理和治疗共识声明》。

Consensus Statement for the Management and Treatment of Port-Wine Birthmarks in Sturge-Weber Syndrome.

机构信息

Department of Dermatology, University of California, Irvine School of Medicine, Irvine.

The Sturge-Weber Foundation, Houston, Texas.

出版信息

JAMA Dermatol. 2021 Jan 1;157(1):98-104. doi: 10.1001/jamadermatol.2020.4226.

Abstract

IMPORTANCE

Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome involving the skin, brain, and eyes. Consensus recommendations for management are lacking.

OBJECTIVE

To consolidate the current literature with expert opinion to make recommendations that will guide treatment and referral for patients with port-wine birthmarks (PWBs).

EVIDENCE REVIEW

In this consensus statement, 12 nationally peer-recognized experts in dermatology with experience treating patients with SWS were assembled. Key topics and questions were formulated for each group and included risk stratification, optimum treatment strategies, and recommendations regarding light-based therapies. A systematic PubMed search was performed of English-language articles published between December 1, 2008, and December 1, 2018, as well as other pertinent studies identified by the expert panel. Clinical practice guidelines were recommended.

FINDINGS

Treatment of PWBs is indicated to minimize the psychosocial impact and diminish nodularity and potentially tissue hypertrophy. Better outcomes may be attained if treatments are started at an earlier age. In the US, pulsed dye laser is the standard for all PWBs regardless of the lesion size, location, or color. When performed by experienced physicians, laser treatment can be safe for patients of all ages. The choice of using general anesthesia in young patients is a complex decision that must be considered on a case-by-case basis.

CONCLUSIONS AND RELEVANCE

These recommendations are intended to help guide clinical practice and decision-making for patients with SWS and those with isolated PWBs and may improve patient outcomes.

摘要

重要性

Sturge-Weber 综合征(SWS)是一种涉及皮肤、大脑和眼睛的神经皮肤综合征。目前缺乏管理的共识建议。

目的

结合现有文献和专家意见,为葡萄酒色痣(PWBs)患者的治疗和转诊提供指导建议。

证据回顾

在这项共识声明中,汇集了 12 名在皮肤科领域具有治疗 SWS 患者经验的全国同行认可的专家。为每个小组制定了关键主题和问题,包括风险分层、最佳治疗策略以及关于光疗的建议。对 2008 年 12 月 1 日至 2018 年 12 月 1 日期间发表的英文文章以及专家组确定的其他相关研究进行了系统的 PubMed 搜索。推荐临床实践指南。

发现

治疗 PWBs 的目的是尽量减少心理社会影响,减少结节和潜在的组织肥大。如果在更早的年龄开始治疗,可能会获得更好的结果。在美国,脉冲染料激光是所有 PWBs 的标准治疗方法,无论病变大小、位置或颜色如何。由经验丰富的医生进行时,激光治疗对所有年龄段的患者都是安全的。在年轻患者中使用全身麻醉的选择是一个复杂的决定,必须根据具体情况考虑。

结论和相关性

这些建议旨在帮助指导 SWS 患者和孤立性 PWBs 患者的临床实践和决策,并可能改善患者的预后。

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