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足月新生儿点状脑白质病变:潜在病因和结局。

Punctate white-matter lesions in the full-term newborn: Underlying aetiology and outcome.

机构信息

Department of Neurology, Royal Children's Hospital, Parkville, Australia; Department of Paediatric Neurology, Monash Children's Hospital, Clayton, Australia; University of Melbourne, Department of Paediatrics, Parkville, Australia; Monash University, Department of Paediatrics, Clayton, Australia; Murdoch Children's Research Institute, Parkville, Australia.

Department of Neonatology, Isala Women & Children's Hospital, Zwolle, the Netherlands.

出版信息

Eur J Paediatr Neurol. 2019 Mar;23(2):280-287. doi: 10.1016/j.ejpn.2019.01.005. Epub 2019 Jan 26.

Abstract

BACKGROUND

Punctate white matter lesions (PWMLs) are small focal patches of increased signal intensity (SI) on T1- and decreased SI on T2-weighted magnetic resonance imaging (MRI). To date, there have been few reports of PWMLs in term born infants.

OBJECTIVE

To identify associated diagnoses and factors predictive of clinical outcome in (near) term infants with PWMLs.

METHODS

MRI studies and clinical records of (near) term infants, with PWMLs on MRI scans performed in two institutions in the first 28 postnatal days were reviewed. The PWMLs were classified according to their number, pattern and distribution. The medical records were examined to assess the associated diagnoses and determine the neurodevelopmental outcome at >12 months of age. Infants with congenital heart defect(s), those who had neonatal surgery, or those with perinatal arterial ischemic stroke were not eligible for the study.

RESULTS

Forty-two (near) term infants with PWMLs were included. The major clinical association was perinatal asphyxia, present in 19/42 (45%). Ten (24%) had a history of seizures unrelated to asphyxia or a genetic diagnosis. Eleven (26%) had pathological genetic mutations. Other diagnoses, without seizures were identified in 2 (5%). The lesion load of PWMLs was high (>6) in 30/42 (71%). Evidence of irreversible white matter injury was present in 5 infants who had follow-up MRI performed between 18 and 24 months of age, because of clinical concerns. Five infants died and 37 had follow-up at a median age of 24 months. Neurodevelopmental outcome was poorest amongst 6 infants (16%) whose PWMLs occurred in the setting of a genetic disorder.

CONCLUSION

PWMLs in (near) term infants represent white matter injury that may evolve into gliosis and/or white matter loss. Infants with PWMLs in the setting of a genetic disorder appeared at most risk of a poor outcome.

摘要

背景

点状脑白质病变(PWMLs)是指在 T1 加权像上呈高信号(SI)、在 T2 加权像上呈低信号的小灶性脑白质病变。迄今为止,关于足月出生婴儿的 PWMLs 报道较少。

目的

确定在两个机构的 28 天内进行的 MRI 扫描中发现 PWMLs 的(近)足月婴儿的相关诊断和预测临床结局的因素。

方法

回顾了在两个机构的 28 天内进行的 MRI 研究和(近)足月婴儿的临床记录,这些婴儿的 MRI 扫描中存在 PWMLs。根据其数量、模式和分布对 PWMLs 进行分类。检查病历以评估相关诊断,并确定 >12 个月时的神经发育结局。患有先天性心脏病(s)、新生儿手术或围产期动脉缺血性卒中的婴儿不符合研究条件。

结果

共纳入 42 例(近)足月婴儿,PWMLs 主要的临床关联是围产期窒息,有 19/42 例(45%)。10 例(24%)有与窒息或遗传诊断无关的癫痫发作史。11 例(26%)存在病理性基因突变。其他无癫痫发作的诊断在 2 例(5%)中发现。42 例中有 30 例(71%)的 PWMLs 病变负荷较高(>6)。由于临床关注,5 例婴儿在 18 至 24 个月时进行了随访 MRI,显示有不可逆的白质损伤证据。5 例婴儿死亡,37 例婴儿在中位数年龄为 24 个月时进行了随访。在 PWMLs 发生在遗传疾病背景下的 6 例婴儿(16%)中,神经发育结局最差。

结论

(近)足月婴儿的 PWMLs 代表白质损伤,可能发展为神经胶质增生和/或白质丢失。在遗传疾病背景下发生 PWMLs 的婴儿似乎面临最严重的不良结局风险。

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