Hausman-Kedem Moran, Widjaja Elysa, Vieira Neto Ronan J, Pope Elena, Lara-Corrales Irene, Dlamini Nomazulu, Macgregor Daune, Pulcine Elizabeth, Deveber Gabrielle, Moharir Mahendranath
Tel Aviv Sourasky Medical Center, Pediatric Neurology Institute, Dana-Dwek Children's Hospital, Tel Aviv, Israel.
Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Dev Med Child Neurol. 2024 Oct;66(10):1348-1360. doi: 10.1111/dmcn.15916. Epub 2024 Apr 10.
To 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.
A 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.
Thirty-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.
In 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.
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.
描述患有后颅窝畸形、血管瘤、动脉异常、主动脉缩窄/心脏缺陷和眼部异常(PHACE)综合征的儿童中风和颅颈血管病变进展的发生率。
一项针对PHACE综合征儿童的单中心回顾性自然病史研究。回顾临床和系列神经影像学数据,以研究血管病变的特征和进展,并计算动脉缺血性中风(AIS)和短暂性缺血性中风(TIA)的发生率。血管病变进展定义为随访磁共振血管造影显示血管情况恶化或出现新的血管病变。
研究了34例在诊断PHACE综合征时伴有脑血管异常的儿童(年龄范围为2至18岁,85%为女性)。初次诊断时的中位年龄为5.5个月(四分位间距为1至52个月);最后一次随访时的中位年龄为8岁6个月(范围为2至18岁)。总体而言,10例(29%)患者的血管病变有影像学进展,累积无进展率为73%(95%置信区间[CI]=0.57至0.89),累积无TIA和无AIS率为87%(95%CI=0.745至0.99)。在最后一次随访时,6例患者(18%)的血管病变呈持续进展。3例患者(9%)发生TIA,且均有进展性血管病变。1例患者在初次诊断PHACE时推测发生围产期AIS,而在随访期间没有其他患者发生AIS。
在患有PHACE综合征的儿童中,大多数情况下颅颈血管病变无进展且无症状。这些儿童发生缺血性中风的风险非常低。需要更大规模的前瞻性研究来证实这些发现。
患有PHACE综合征的儿童脑血管病变主要无进展且无症状。患有PHACE综合征的儿童脑血管病变与儿童期中风风险低相关。在患有进展性血管病变的儿童中,神经影像学进展在生命的最初几年通常较为缓慢。