Clinical features and neuroimaging (CT and MRI) findings in presumed Zika virus related congenital infection and microcephaly: retrospective case series study

• Autores: Maria de Fatima Vasco Aragao, Vanessa Vander Linden, Alessandra Mertens Brainer Lima, Regina Ramos Coeli, María Teresa Rocha, Paula Sobral, Maria Durce Costa Gomes, Ana Vander Linden, Arthur Cesario de Holanda, Marcelo Moraes Valenca
• Localización: BMJ, ISSN-e 0959-535X, Vol. 352, Nº. 5, 2016
• Idioma: inglés
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• Resumen

  • Objective To report radiological findings observed in computed tomography (CT) and magnetic resonance imaging (MRI) scans of the first cases of congenital infection and microcephaly presumably associated with the Zika virus in the current Brazilian epidemic.

    Design Retrospective study with a case series.

    Setting Association for Assistance of Disabled Children (AACD), Pernambuco state, Brazil.

    Participants 23 children with a diagnosis of congenital infection presumably associated with the Zika virus during the Brazilian microcephaly epidemic.

    Main outcome measures Types of abnormalities and the radiological pattern of lesions identified on CT and MRI brain scans.

    Results Six of the 23 children tested positive for IgM antibodies to Zika virus in cerebrospinal fluid. The other 17 children met the protocol criteria for congenital infection presumably associated with the Zika virus, even without being tested for IgM antibodies to the virus—the test was not yet available on a routine basis.

    Of the 23 children, 15 underwent CT, seven underwent both CT and MRI, and one underwent MRI. Of the 22 children who underwent CT, all had calcifications in the junction between cortical and subcortical white matter, 21 (95%) had malformations of cortical development, 20 (91%) had a decreased brain volume, 19 (86%) had ventriculomegaly, and 11 (50%) had hypoplasia of the cerebellum or brainstem. Of the eight children who underwent MRI, all had calcifications in the junction between cortical and subcortical white matter, malformations of cortical development occurring predominantly in the frontal lobes, and ventriculomegaly. Seven of the eight (88%) children had enlarged cisterna magna, seven (88%) delayed myelination, and six each (75%) a moderate to severe decrease in brain volume, simplified gyral pattern, and abnormalities of the corpus callosum (38% hypogenesis and 38% hypoplasia).

    Malformations were symmetrical in 75% of the cases.