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

Abstract

<b>Objective</b>&nbsp;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. <b>Design</b>&nbsp;Case series study. <b>Setting</b>&nbsp;Barão de Lucena Hospital, Pernambuco state, Brazil. <b>Participants</b>&nbsp;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. <b>Main outcome measure</b>&nbsp;Differences in cerebral calcification patterns between initial and follow-up scans. <b>Results</b>&nbsp;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. <b>Conclusion</b>&nbsp;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.