Congenital Zika virus syndrome...what else? Two case reports of severe combined fetal pathologies

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 etiolog...

Full description

Saved in:
Bibliographic Details
Main Authors: Manon Vouga (Author), David Baud (Author), Eugénie Jolivet (Author), Fatiha Najioullah (Author), Alice Monthieux (Author), Bruno Schaub (Author)
Format: Book
Published: BMC, 2018-09-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_9bf61a4f424b41f6afcda9f11d2766e4
042 |a dc 
100 1 0 |a Manon Vouga  |e author 
700 1 0 |a David Baud  |e author 
700 1 0 |a Eugénie Jolivet  |e author 
700 1 0 |a Fatiha Najioullah  |e author 
700 1 0 |a Alice Monthieux  |e author 
700 1 0 |a Bruno Schaub  |e author 
245 0 0 |a Congenital Zika virus syndrome...what else? Two case reports of severe combined fetal pathologies 
260 |b BMC,   |c 2018-09-01T00:00:00Z. 
500 |a 10.1186/s12884-018-1998-4 
500 |a 1471-2393 
520 |a 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. 
546 |a EN 
690 |a Congenital Zika syndrome 
690 |a Parvovirus B19 
690 |a Trisomy 18 
690 |a Microcephaly 
690 |a Fetal anemia 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-6 (2018) 
787 0 |n http://link.springer.com/article/10.1186/s12884-018-1998-4 
787 0 |n https://doaj.org/toc/1471-2393 
856 4 1 |u https://doaj.org/article/9bf61a4f424b41f6afcda9f11d2766e4  |z Connect to this object online.