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dc.contributor.authorCelik H.
dc.contributor.authorKefeli M.
dc.contributor.authorTosun M.
dc.contributor.authorÇetinkaya M.B.
dc.contributor.authorAlper T.
dc.contributor.authorYildiz L.
dc.date.accessioned2020-06-21T09:28:08Z
dc.date.available2020-06-21T09:28:08Z
dc.date.issued2009
dc.identifier.issn8756-4793
dc.identifier.urihttps://doi.org/10.1177/8756479309333107
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4247
dc.description.abstractCongenital mesoblastic nephroma is a rare renal tumor of early infancy with a favorable outcome after complete surgical removal. It consists of a heterogeneous group of spindle cell tumors. Early and accurate prenatal diagnosis of the renal tumor may improve the outcome of affected pregnancies by implementing the best strategy for prenatal management and delivery. But detection of congenital mesoblastic nephroma in a fetus is rare. To the authors' knowledge, there are fewer than 30 reports of a prenatal diagnosis of a mesoblastic nephroma in the literature. This case describes the prenatal sonographic diagnosis of cellular congenital mesoblastic nephroma.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1177/8756479309333107en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCongenital mesoblastic nephromaen_US
dc.subjectPrenatal diagnosisen_US
dc.subjectUltrasonographyen_US
dc.titleCongenital mesoblastic nephroma: Prenatal diagnosis by sonographyen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume25en_US
dc.identifier.issue2en_US
dc.identifier.startpage112en_US
dc.identifier.endpage115en_US
dc.relation.journalJournal of Diagnostic Medical Sonographyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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