Long‐term clinical and radiological trajectories of craniocervical vasculopathy in children with PHACE syndrome

Author:

Hausman‐Kedem Moran12ORCID,Widjaja Elysa34ORCID,Vieira Neto Ronan J.5,Pope Elena6,Lara‐Corrales Irene6,Dlamini Nomazulu7ORCID,Macgregor Daune7,Pulcine Elizabeth7,Deveber Gabrielle7,Moharir Mahendranath7ORCID

Affiliation:

1. Tel Aviv Sourasky Medical Center Pediatric Neurology Institute, Dana‐Dwek Children's Hospital Tel Aviv Israel

2. Faculty of Medicine Tel Aviv University Tel Aviv Israel

3. Division of Neuroradiology, Department of Diagnostic Imaging The Hospital for Sick Children Toronto ON Canada

4. Department of Medical Imaging Ann & Robert H. Lurie Children's Hospital Chicago USA

5. Department of Pediatric Neurology Hospital Sírio‐Libanês São Paulo Brazil

6. Division of Dermatology, Department of Pediatrics Hospital for Sick Children Toronto ON Canada

7. Children's Stroke Program, Division of Neurology, Department of Pediatrics The Hospital for Sick Children Toronto ON Canada

Abstract

AbstractAimTo describe the rates of stroke and craniocervical vasculopathy progression in children with posterior fossa malformations, hemangioma, arterial anomalies, coarctation of the aorta/cardiac defects, and eye abnormalities (PHACE) syndrome.MethodA single‐center, retrospective natural history study of children with PHACE syndrome. Clinical and sequential neuroimaging data were reviewed to study the characteristics and progression of vasculopathy and calculate the rates of arterial ischemic stroke (AIS) and transient ischemic stroke (TIA). Vasculopathy progression was defined as worsening or new vascular findings on follow‐up magnetic resonance angiography.ResultsThirty‐four children with cerebrovascular abnormalities at the PHACE syndrome diagnosis were studied (age range = 2 to 18 years, 85% females). Median age at the initial diagnosis was 5.5 months (interquartile range = 1–52 months); median age at the last follow‐up was 8 years 6 months (range = 2–18 years). Overall, 10 (29%) patients had radiological progression of their vasculopathy, with a cumulative progression‐free rate of 73% (95% confidence interval [CI] = 0.57–0.89), and a cumulative TIA‐free and AIS‐free rate of 87% (95% CI = 0.745–0.99). Vasculopathy was continuously progressive in six patients (18%) at the last follow‐up. Three patients (9%) had TIA and all had progressive vasculopathy. One patient had presumed perinatal AIS at the initial PHACE diagnosis, while no other patient experienced an AIS during the follow‐up.InterpretationIn children with PHACE syndrome, craniocervical vasculopathy is non‐progressive and asymptomatic in the majority of cases. The risk of ischemic stroke in these children is very low. Larger and prospective studies are necessary to confirm these findings.What this paper adds Cerebrovascular vasculopathy in children with PHACE syndrome is predominantly non‐progressive and asymptomatic. Cerebrovascular vasculopathy in children with PHACE syndrome is associated with a low risk of stroke during childhood. In children with progressive vasculopathy, neuroimaging progression was generally slow over the first years of life.

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Are repeat neuroimaging studies needed in PHACE syndrome?;Developmental Medicine & Child Neurology;2024-04-24

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3