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Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies.
Vouga, Manon; Baud, David; Jolivet, Eugénie; Najioullah, Fatiha; Monthieux, Alice; Schaub, Bruno.
Afiliação
  • Vouga M; Materno-Fetal and Obstetrics Research Unit, Department « Femme-Mère-Enfant ¼, University Hospital, Lausanne, Switzerland.
  • Baud D; Materno-Fetal and Obstetrics Research Unit, Department « Femme-Mère-Enfant ¼, University Hospital, Lausanne, Switzerland. david.baud@chuv.ch.
  • Jolivet E; Materno-fetal & Obstetrics Research Unit, Department of Obstetrics and Gynecology, Centre Hospitalier Universitaire Vaudois (CHUV), 1011, Lausanne, Switzerland. david.baud@chuv.ch.
  • Najioullah F; Multidisciplinary Center of Prenatal Diagnosis of Martinique, Unit of Obstetrics and Gynecology, Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort de France, France.
  • Monthieux A; Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort de France, France.
  • Schaub B; Service de Virologie, University Hospital of Martinique, Fort de France, France.
BMC Pregnancy Childbirth ; 18(1): 356, 2018 Sep 03.
Article em En | MEDLINE | ID: mdl-30176812
ABSTRACT

BACKGROUND:

Zika virus (ZIKV) has recently emerged as a teratogenic infectious agent associated with severe fetal cerebral anomalies. Other microorganisms (TORCH agents) as well as genetic disorders and toxic agents may lead to similar anomalies. In case of fetal anomalies, the exact etiology might be difficult to establish, especially in ZIKV endemic countries. As the risks associated with maternal infection remain unclear adequate parental counseling is difficult. CASE PRESENTATION We present two cases of severe fetal pathologies managed in our multidisciplinary center during the ZIKV outbreak in Martinique, a French Caribbean Island. Both fetuses had congenital ZIKV infection confirmed by RT-PCR. While one case presented with significant cerebral anomalies, the other one presented with hydrops fetalis. A complete analysis revealed that the fetal lesions observed resulted from a combination of ZIKV congenital infection and a genetic disorder (trisomy 18) in case 1 or congenital Parvovirus B19 infection in case 2.

CONCLUSIONS:

We highlight the difficulties related to adequate diagnosis in case of suspected ZIKV congenital syndrome. Additional factors may contribute to or cause fetal pathology, even in the presence of a confirmed ZIKV fetal infection. An exact diagnosis is mandatory to draw definitive conclusions. We further emphasize that, similarly to other congenital infections, it is very likely that not all infected fetuses will become symptomatic.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Parvoviridae / Zika virus / Infecção por Zika virus / Síndrome da Trissomía do Cromossomo 18 Limite: Humans / Newborn Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Parvoviridae / Zika virus / Infecção por Zika virus / Síndrome da Trissomía do Cromossomo 18 Limite: Humans / Newborn Idioma: En Ano de publicação: 2018 Tipo de documento: Article