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dc.contributor.authorÇakmak, M.
dc.contributor.authorSavaş, C.
dc.contributor.authorÖzbaşar, D.
dc.contributor.authorÇandır, O.
dc.contributor.authorKaya, H.
dc.contributor.authorCağlayan, F.
dc.date.accessioned2020-06-25T17:34:52Z
dc.date.available2020-06-25T17:34:52Z
dc.date.issued2001
dc.identifier.citationclosedAccessen_US
dc.identifier.issn0022-3468
dc.identifier.urihttps://doi.org/10.1053/jpsu.2001.22302
dc.identifier.urihttps://hdl.handle.net/20.500.12587/2931
dc.descriptionSavas, Mustafa Cagri/0000-0001-6454-5323en_US
dc.descriptionWOS: 000167792300018en_US
dc.descriptionPubMed: 11283890en_US
dc.description.abstractThe most common site of teratomas in neonates is in the sacrococcygeal region. Herein the authors describe a congenital teratoma, and to their knowledge it is the first reported case of vulvar site in a newborn. Tumor was removed on the fourth day of life, and she was completely normal 18 months after the operation. Because of possible malignancy or recurrence, complete surgical excision of the tumor and the careful follow-up is the treatment of choice. Copyright (C) 2001 by W.B. Saunders Company.en_US
dc.language.isoengen_US
dc.publisherW B Saunders Coen_US
dc.relation.isversionof10.1053/jpsu.2001.22302en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectteratomaen_US
dc.subjectvulvaen_US
dc.titleCongenital vulvar teratoma in a newbornen_US
dc.typeeditorialen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume36en_US
dc.identifier.issue4en_US
dc.identifier.startpage620en_US
dc.identifier.endpage621en_US
dc.relation.journalJournal Of Pediatric Surgeryen_US
dc.relation.publicationcategoryDiğeren_US


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