Literature DB >> 29209885

Neuroimaging findings associated with congenital Zika virus syndrome: case series at the time of first epidemic outbreak in Pernambuco State, Brazil.

Pedro Pires1, Patricia Jungmann2, Jully Moura Galvão1, Adriano Hazin3, Luiza Menezes1, Ricardo Ximenes4, Gabriele Tonni5, Edward Araujo Júnior6.   

Abstract

PURPOSE: This study aimed to describe the prenatal and postnatal neuroimaging and clinical findings in a clinical series following congenital Zika virus syndrome during the first epidemic Zika virus (ZIKV) outbreak in the State of Pernambuco, Brazil.
METHODS: We (the authors) conducted a retrospective study of a prospectively collected case series of fetuses and neonates with microcephaly born to mothers with presumed/confirmed congenital ZIKV syndrome. Prenatal ultrasound findings were reviewed to identify potential central nervous system (CNS) abnormalities. Neonates underwent postnatal neuroimaging follow up by computed tomography (CT)-scan or magnetic resonance (MR) imaging.
RESULTS: The prenatal and postnatal outcomes of eight fetuses/neonates born to mothers with presumed/confirmed congenital ZIKV syndrome were examined. The mean gestational age at ultrasound was 31.3 weeks. Severe microcephaly was identified in seven fetuses (87.5%), while ventriculomegaly and brain calcifications were detected in all fetuses. The mean gestational age at delivery and head circumference were 38 weeks and 30.2 cm, respectively. All cases of microcephaly but one was confirmed postnatally. Brain CT scans or MRIs were performed in seven newborns, and all had periventricular and/or parenchymal calcifications, symmetrical or asymmetrical ventriculomegaly, pachygyria, and reduced sulcation and gyration. MR imaging aided the detection of one undetected case of corpus callosum dysgenesis and was essential in documenting reduced mantel of the cerebral cortex and reduced gyration and sulcation, especially involving the parietal lobe. In addition, MR imaging was also able to display irregular interfaces with the subcortical white matter, a finding consistent with polymicrogyria, more frequently seen at the level of the frontal lobe and atrophic and thinned pons.
CONCLUSION: Severe microcephaly and CNS abnormalities may be associated with congenital ZIKV syndrome.

Entities:  

Keywords:  Brain abnormalities; Computed tomography; Congenital Zika virus syndrome; Magnetic resonance imaging; Microcephaly; Ultrasound

Mesh:

Year:  2017        PMID: 29209885     DOI: 10.1007/s00381-017-3682-9

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.532


  20 in total

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Authors:  R Alagappan; P D Browning; A Laorr; J P McGahan
Journal:  Radiology       Date:  1994-11       Impact factor: 11.105

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Journal:  Radiology       Date:  1984-02       Impact factor: 11.105

3.  Congenital Brain Abnormalities and Zika Virus: What the Radiologist Can Expect to See Prenatally and Postnatally.

Authors:  Patricia Soares de Oliveira-Szejnfeld; Deborah Levine; Adriana Suely de Oliveira Melo; Melania Maria Ramos Amorim; Alba Gean M Batista; Leila Chimelli; Amilcar Tanuri; Renato Santana Aguiar; Gustavo Malinger; Renato Ximenes; Richard Robertson; Jacob Szejnfeld; Fernanda Tovar-Moll
Journal:  Radiology       Date:  2016-08-23       Impact factor: 11.105

4.  Associated ultrasonographic findings in fetuses with microcephaly because of suspected Zika virus (ZIKV) infection during pregnancy.

Authors:  Francisco Herlânio Costa Carvalho; Kárita Melo Cordeiro; Alberto Borges Peixoto; Gabriele Tonni; Antonio Fernandes Moron; Francisco Edson Lucena Feitosa; Helvécio Neves Feitosa; Edward Araujo Júnior
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7.  Interim Guidelines for the Evaluation and Testing of Infants with Possible Congenital Zika Virus Infection - United States, 2016.

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Review 8.  Congenital Zika syndrome and neuroimaging findings: what do we know so far?

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Authors:  Zachary A Klase; Svetlana Khakhina; Adriano De Bernardi Schneider; Michael V Callahan; Jill Glasspool-Malone; Robert Malone
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7.  Zika virus infection as a cause of congenital brain abnormalities and Guillain-Barré syndrome: A living systematic review.

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  8 in total

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