Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/11181
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dc.contributor.authorBaştuğ, Osman-
dc.contributor.authorÖztürk, Mehmet Adnan-
dc.contributor.authorHalis, Hülya-
dc.contributor.authorMemur, Şeyma-
dc.contributor.authorKorkmaz, Levent-
dc.contributor.authorKurtoğlu, Selim-
dc.contributor.authorAkgün, Hülya-
dc.date.accessioned2020-06-14T18:59:19Z-
dc.date.available2020-06-14T18:59:19Z-
dc.date.issued2015-03-03-
dc.identifier.citationBaştuğ, O. vd. (2016). "Yenidoğanda intraoral kitlenin nadir bir sebebi: Konjenital epulis". Güncel Pediatri, 14(3), 147-150.tr_TR
dc.identifier.issn1304-9054-
dc.identifier.issn1308-6308-
dc.identifier.urihttps://dergipark.org.tr/tr/download/article-file/902863-
dc.identifier.urihttp://hdl.handle.net/11452/11181-
dc.description.abstractKonjenital epulis, yenidoğanın granüler hücreli tümörü veya Neumann’s tümörü olarak da bilinen, yenidoğanın çenesinde görülen nadir konjenital bir tümördür. 10:1 oranında kızlarda daha sık görülür. Lezyon benign karakterdedir. Rekürrens veya metastaz rapor edilmemiştir. Olgumuzda konjenital epulis maksillar alveolar çıkıntının kesici diş bölgesinde yer almıştır. Prenatal takiplerinde problem olmayan ancak doğumda ağız içerisinde kitle sebebiyle başvuran hastada nadir görülen konjenital epulis tanısı konuldu. Lezyon beslenmeye engel olduğu için genel anestezi altında çıkarıldı. İntraoperatif ve postoperatif takiplerinde problem yaşanmadı. Takip eden üç ayda rekürrens görülmedi.tr_TR
dc.description.abstractCongenital epulis, also known as granular cell tumor of the newborn or Neumann’s tumor, is a rare congenital tumor affecting the gingival mucosa of neonates. It occurs more often in female population with the ratio of 10:1. These lesions behave in a benign manner. No recurrence or metastasis have been reported. The present case had congenital epulis in the incisor region of maxillary alveolar ridge. The patient had no problem at prenatal follow-up, but applied to the clinic with a mass in the mouth at birth and diagnosed as with congenital epulis. Since this lesion interferes with nourishment, it was excised under general anaesthesia. There was no problem at intraoperative and postoperative course. No recurrence was seen in the following 3 months.en_US
dc.language.isotrtr_TR
dc.publisherUludağ Üniversitesitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectKonjenital epulistr_TR
dc.subjectGranüler hücreli tümörtr_TR
dc.subjectİnfanttr_TR
dc.subjectCongenital epulisen_US
dc.subjectGranular cell tumoren_US
dc.subjectInfanten_US
dc.titleYenidoğanda intraoral kitlenin nadir bir sebebi: Konjenital epulistr_TR
dc.title.alternativeA rare cause of the intraoral mass in a newborn infant: Congenital epulisen_US
dc.typeArticleen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.identifier.startpage147tr_TR
dc.identifier.endpage150tr_TR
dc.identifier.volume14tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalGüncel Pediatri / The Journal of Current Pediatricstr_TR
Appears in Collections:2016 Cilt 14 Sayı 3

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