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dc.contributor.authorBaşak, Kayhan
dc.contributor.authorAydın, Sedat
dc.contributor.authorBaşak, Pınar
dc.contributor.authorDEMİR, Mehmet Gökhan
dc.contributor.authorDemir, Hicran Ozdemir
dc.date.accessioned2021-03-04T12:44:43Z
dc.date.available2021-03-04T12:44:43Z
dc.identifier.citationDEMİR M. G. , Aydın S., Başak K., Başak P., Demir H. O. , "Nasal Congenital Panfollicular Nevus", INDIAN JOURNAL OF OTOLARYNGOLOGY AND HEAD & NECK SURGERY, cilt.71, ss.1705-1707, 2019
dc.identifier.issn2231-3796
dc.identifier.othervv_1032021
dc.identifier.otherav_78df4578-e47c-4111-b0e0-9046e09b93c3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/82871
dc.identifier.urihttps://doi.org/10.1007/s12070-016-0996-y
dc.description.abstractCongenital nasal midline lesions are rarely observed pathologies. While relatively frequently encountered lesions are dermoid cyst, glioma, encephalocele, nasal polyp and epidermoid cyst, an other very rare reason is the congenital panfollicular nevus. The treatment of this syndrome appearing with a recurrent discharge in clinic is the surgical excision. We will hereby present the excision of the case of congenital panfollicular nevus with three different fistula openings.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCERRAHİ
dc.titleNasal Congenital Panfollicular Nevus
dc.typeMakale
dc.relation.journalINDIAN JOURNAL OF OTOLARYNGOLOGY AND HEAD & NECK SURGERY
dc.contributor.departmentAnkara Yıldırım Beyazıt Üniversitesi , ,
dc.identifier.volume71
dc.identifier.startpage1705
dc.identifier.endpage1707
dc.contributor.firstauthorID727625


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