Follow-up brain imaging of 37 children with congenital Zika syndrome: case series study
Autor(es): Petribu, Natacha Calheiros de Lima; Vasco, Aragão Maria de Fatima; Linden, Vanessa van der; Parizel, Paul; Jungmann, Patricia; Araújo, Luziany; Abath, Marília; Fernandes, Andrezza; Brainer-Lima, Alessandra; Holanda, Arthur; Mello, Roberto; Sarteschi, Camila; Duarte, Maria do Carmo Menezes Bezerra
Resumo: 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. Case series study. Barão de Lucena Hospital, Pernambuco state, Brazil. 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. Differences in cerebral calcification patterns between initial and follow-up scans. 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. 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.
Imprenta: BMJ, v. 359, 2017
Identificador do objeto digital: 10.1136/bmj.j4188
Descritores: Zika virus - Pathogenesis
Data de publicação: 2017
