Stridor in a newborn caused by a congenital laryngocele and bifid epiglottis: A case report and review of the literature

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dc.contributor.authorYılmaz, Süleyman
dc.contributor.authorYıldızbaş, Şahnur
dc.contributor.authorYaman, Hüseyin
dc.contributor.authorGüçlü, Ender
dc.contributor.authorÖztürk, Özcan
dc.date.accessioned2020-04-30T13:33:27Z
dc.date.available2020-04-30T13:33:27Z
dc.date.issued2010
dc.departmentDÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.description.abstractA laryngocele is a rare, an abnormal cystic dilatation of the laryngeal saccule. A bifid epiglottis is also an extremely rare congenital anomaly of larynx that is often associated with other congenital defects. In this article, we report a case of an internal laryngocele and bifid epiglottis in a one hour old newborn girl that presented as acute airway obstruction who also have imperforate hymen, hydrocolpos, bilateral hydronephrosis and polydactyly. The patient underwent endoscopic microsurgical excision of internal laryngocele using suspension laryngoscopy and cold blade. We also review the anatomy, etiology and clinic course of the different types of laryngoceles, bifid epiglottis and related congenital defects. © 2009 Elsevier Ireland Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.pedex.2009.01.003en_US
dc.identifier.endpage31en_US
dc.identifier.issn1871-4048
dc.identifier.issue1en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage28en_US
dc.identifier.urihttps://dx.doi.org/10.1016/j.pedex.2009.01.003
dc.identifier.urihttps://hdl.handle.net/20.500.12684/643
dc.identifier.volume5en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofInternational Journal of Pediatric Otorhinolaryngology Extraen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAirway obstruction; Bifid epiglottis; Congenital laryngocele; Endoscopic resectionen_US
dc.titleStridor in a newborn caused by a congenital laryngocele and bifid epiglottis: A case report and review of the literatureen_US
dc.typeArticleen_US

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