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Follow-up brain imaging of 37 children with congenital Zika syndrome: case series study

机译:37例先天性寨卡综合征儿童的随访脑成像:病例系列研究

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摘要

>Objective To compare initial brain computed tomography (CT) scans with follow-up CT scans at one year in children with congenital Zika syndrome, focusing on cerebral calcifications. >Design Case series study. >Setting Barão de Lucena Hospital, Pernambuco state, Brazil. >Participants 37 children with probable or confirmed congenital Zika syndrome during the microcephaly outbreak in 2015 who underwent brain CT shortly after birth and at one year follow-up. >Main outcome measure Differences in cerebral calcification patterns between initial and follow-up scans. >Results 37 children were evaluated. All presented cerebral calcifications on the initial scan, predominantly at cortical-white matter junction. At follow-up the calcifications had diminished in number, size, or density, or a combination in 34 of the children (92%, 95% confidence interval 79% to 97%), were no longer visible in one child, and remained unchanged in two children. No child showed an increase in calcifications. The calcifications at the cortical-white matter junction which were no longer visible at follow-up occurred predominately in the parietal and occipital lobes. These imaging changes were not associated with any clear clinical improvements. >Conclusion The detection of cerebral calcifications should not be considered a major criterion for late diagnosis of congenital Zika syndrome, nor should the absence of calcifications be used to exclude the diagnosis.
机译:>目的将先天性寨卡综合征患儿的最初的计算机X线断层扫描(CT)与随访的CT扫描进行比较,重点是脑钙化。 >设计案例研究。 >设置,巴西伯南布哥州巴拉诺德卢塞纳医院。 >参与者:在2015年小头症暴发期间,37例可能或确诊的先天性寨卡综合症患儿在出生后不久和一年的随访中接受了脑部CT检查。 >主要结局指标:初次与随访之间脑钙化模式的差异。 >结果。对37名儿童进行了评估。所有患者均在初次扫描时出现脑钙化,主要在皮质-白质交界处。随访时,钙化的数量,大小或密度降低,或其中34名儿童的合并钙化(92%,95%置信区间79%至97%),一个孩子不再可见,并且保持不变有两个孩子没有儿童显示钙化增加。皮质白质交界处的钙化在随访中不再可见,主要发生在顶叶和枕叶。这些影像学改变与任何明显的临床改善无关。 >结论:脑钙化的检测不应被视为先天性寨卡综合征晚期诊断的主要标准,也不应将钙化的缺乏排除在诊断之外。

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