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美国明尼苏达州奥姆斯特德县的 Sturge-Weber 综合征发病率及其相关眼部受累情况。

Incidence of Sturge-Weber syndrome and associated ocular involvement in Olmsted County, Minnesota, United States.

机构信息

Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota, USA.

Department of Health Sciences Research, Mayo Clinic, Jacksonville, Florida, USA.

出版信息

Ophthalmic Genet. 2020 Apr;41(2):108-124. doi: 10.1080/13816810.2020.1731834. Epub 2020 Mar 31.

Abstract

: Sturge-Weber syndrome (SWS) is a rare sporadic syndrome characterized by nevus flammeus (port-wine stain, PWS) in the trigeminal nerve distribution, diffuse choroidal hemangioma, and brain leptomeningeal hemangioma. We are unaware of previous reports of SWS incidence in the United States. This study investigated SWS incidence and associated ocular involvement in Olmsted County, Minnesota.: The Rochester Epidemiology Project database was used to identify SWS cases from January 1, 2000-December 31, 2017. Incidence of SWS was calculated using the Olmsted County census population. A literature review of studies investigating SWS-associated ocular involvement was also performed.: There were 13 patients with SWS in Olmsted County classified as type 1 (31%) or type 2 (69%). Age and sex-adjusted incidence of SWS was 0.19/100,000/year. Race was predominantly Caucasian (85%), with sex female (69%) or male (31%). All patients had PWS, mostly with unilateral distribution in the V1 and/or V2 region (85%). Two cases (15%) had associated Klippel-Trenaunay syndrome. The most common ocular features included: dilated episcleral vessels (46%), glaucoma (46%), retinal detachment (23%), DCH (7.7%), strabismus (31%), and refractive error (38%). PWS in the V1 distribution was associated with all cases of glaucoma, DCH, and neurological involvement. Severe visual impairment (>0.6 LogMAR, Snellen equivalent ≤20/100) was found in (23%) at final follow-up, and one patient (8%) required enucleation for uncontrolled glaucoma.: SWS affects approximately 0.19/100,000/year in Olmsted County. Early diagnosis, intervention, lifelong follow-up, and multidisciplinary approach should be used to optimize systemic and ocular outcomes.

摘要

斯特奇-韦伯综合征(SWS)是一种罕见的散发性综合征,其特征为三叉神经分布区的焰状痣(葡萄酒色痣,PWS)、弥漫性脉络膜血管瘤和脑软脑膜血管瘤。我们不知道以前有关于美国 SWS 发病率的报告。本研究调查了明尼苏达州奥姆斯特德县的 SWS 发病率和相关眼部受累情况。使用罗切斯特流行病学项目数据库从 2000 年 1 月 1 日至 2017 年 12 月 31 日确定 SWS 病例。使用奥姆斯特德县人口普查计算 SWS 的发病率。还对研究 SWS 相关眼部受累的文献进行了综述。在奥姆斯特德县有 13 名 SWS 患者分为 1 型(31%)或 2 型(69%)。年龄和性别调整后的 SWS 发病率为 0.19/100000/年。种族主要为白种人(85%),性别为女性(69%)或男性(31%)。所有患者均有 PWS,主要分布在 V1 和/或 V2 区单侧(85%)。2 例(15%)合并 Klippel-Trenaunay 综合征。最常见的眼部特征包括:巩膜血管扩张(46%)、青光眼(46%)、视网膜脱离(23%)、DCH(7.7%)、斜视(31%)和屈光不正(38%)。V1 分布的 PWS 与所有青光眼、DCH 和神经受累病例相关。在最终随访时,发现(23%)患者视力严重受损(>0.6 LogMAR,Snellen 等价物≤20/100),1 例(8%)患者因无法控制的青光眼需要眼球摘除。奥姆斯特德县 SWS 的发病率约为 0.19/100000/年。应采用早期诊断、干预、终身随访和多学科方法,以优化全身和眼部结局。

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