Abstract

The aim of the current review is to present a systematic evaluation of reported human placental findings in cases of zika virus (ZIKV) infection. We reviewed the EMBASE, PUBMED, and SCIELO databases until June 2019, without language restrictions. The search terms placenta AND zika virus were used. The inclusion criteria of the studies were studies that reported placental findings in humans. Experimental studies, reviews, notes or editorials were excluded. A total of 436 studies were retrieved; after duplicate exclusion, 243 articles had their titles screened, and 128 had their abstract read; of those, 32 were included in the final analysis (18 case reports, 10 case series, and 4 cohorts) DATA COLLECTION: We collected data concerning the author, year of publication, study design, number of participants, number of placental samples, onset of symptoms, perinatal outcomes, and main findings on histological analysis. The placental pathologic findings were described as mild and nonspecific, similar to those of other placental infections, including chronic placentitis, chronic villitis, increased Hofbauer cells, irregular fibrin deposits, increased mononuclear cells in the villus stroma, villous immaturity, edema, hypervascularization, stromal fibrosis, calcification, and focal necrosis of syncytiotrophoblasts. Zika infection presents unspecific placental findings, similar to other infections in the toxoplasmosis, other agents, rubella, cytomegalovirus, and herpes (TORCH)group. Characterizing and standardizing placental findings after zika virus infection is key to understanding the mechanisms of congenital diseases.

Highlights

  • Zika virus (ZIKV) is a flavivirus much similar to other arboviruses of relevance, such as dengue, West Nile, yellow fever, and Japanese encephalitis viruses

  • The aim of the current review is to present a systematic evaluation of reported human placental findings in cases of zika virus (ZIKV) infection

  • Characterizing and standardizing placental findings after zika virus infection is key to understanding the mechanisms of congenital diseases

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Summary

Introduction

Zika virus (ZIKV) is a flavivirus much similar to other arboviruses of relevance, such as dengue, West Nile, yellow fever, and Japanese encephalitis viruses. It is transmitted mostly by Aedes aegypti mosquitoes, and was first recognized in humans in Uganda in 1952, with two main previous outbreaks, in Yap, Micronesia, in 2007 and in the French Polynesia, in 2013.1,2 The ZIKV may be transmitted to humans according to other routes non-vector reliant, such as blood transfusion, sexual transmission, or maternal-fetal transmission.[3]. After the Brazilian zika outbreak, some authors have suggested the inclusion of ZIKV among the group “others” in the acronym or even a more direct inclusion such as TORCHZ.[6]

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