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Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122623/ https://www.ncbi.nlm.nih.gov/pubmed/30176812 http://dx.doi.org/10.1186/s12884-018-1998-4 |
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author | Vouga, Manon Baud, David Jolivet, Eugénie Najioullah, Fatiha Monthieux, Alice Schaub, Bruno |
author_facet | Vouga, Manon Baud, David Jolivet, Eugénie Najioullah, Fatiha Monthieux, Alice Schaub, Bruno |
author_sort | Vouga, Manon |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6122623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61226232018-09-05 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 BMC Pregnancy Childbirth Case Report 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. BioMed Central 2018-09-03 /pmc/articles/PMC6122623/ /pubmed/30176812 http://dx.doi.org/10.1186/s12884-018-1998-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Vouga, Manon Baud, David Jolivet, Eugénie Najioullah, Fatiha Monthieux, Alice Schaub, Bruno Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title | Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title_full | Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title_fullStr | Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title_full_unstemmed | Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title_short | Congenital Zika virus syndrome…what else? Two case reports of severe combined fetal pathologies |
title_sort | congenital zika virus syndrome…what else? two case reports of severe combined fetal pathologies |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122623/ https://www.ncbi.nlm.nih.gov/pubmed/30176812 http://dx.doi.org/10.1186/s12884-018-1998-4 |
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