Publication:
Prenatal diagnosis of sacrococcygeal teratoma

dc.contributor.authorsCoşar E., Sezen D., Gökaslan H., Kavak Z.N.
dc.date.accessioned2022-03-28T14:51:59Z
dc.date.accessioned2026-01-11T16:01:02Z
dc.date.available2022-03-28T14:51:59Z
dc.date.issued2003
dc.description.abstractSacrococcygeal teratoma is a rare fetal neoplasm with an incidence of 1 in 40,000 births. Fetuses with this malformation are at risk of significant perinatal morbidity and mortality. Prenatal ultrasonographic diagnosis of sacrococcygeal teratomas is essential to detect various prenatal and perinatal complications as well as fetal outcome. Adverse clinical sequelae of a sacrococcygeal teratoma can be prevented by accurate prenatal assessment and appropriate obstetrical and perinatal management. Development of fetal hydrops and/or placentomegaly predicts fetal demise. Herein, we present a case of fetal sacrococcygeal teratoma diagnosed prenatally.
dc.identifier.issn10191941
dc.identifier.urihttps://hdl.handle.net/11424/255780
dc.language.isoeng
dc.relation.ispartofMarmara Medical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPrenatal diagnosis
dc.subjectSacrococcygeal teratoma
dc.titlePrenatal diagnosis of sacrococcygeal teratoma
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage54
oaire.citation.issue1
oaire.citation.startPage52
oaire.citation.titleMarmara Medical Journal
oaire.citation.volume16

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