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dc.contributor.authorYılmaz, Rukiye
dc.contributor.authorBedir, Recep
dc.contributor.authorŞehitoğlu, İbrahim
dc.contributor.authorDursun, Engin
dc.date.accessioned2020-12-19T20:51:35Z
dc.date.available2020-12-19T20:51:35Z
dc.date.issued2017
dc.identifier.citationYılmaz, R., Bedir, R., Şehitoğlu, İ. (2017). Salivary gland choristoma of the larynx. Balkan Medical Journal, 34(3), 288-289.
dc.identifier.issn2146-3123
dc.identifier.issn2146-3131
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TWpJM05UWTBOQT09
dc.identifier.urihttps://hdl.handle.net/11436/6076
dc.description.abstractTo the Editor, Choristoma is defined as the presence of histologically normal cells in abnormal locations due to defects during embryological development (1). The criteria for the diagnosis of choristoma are a tumour-like growth, an ectopic tissue with a normal pattern and without neoplastic features histologically, and a mislocated tissue topographically. It is different from hamartoma because the hamartoma appears in normal locations. Laryngeal choristomas are rare lesions and are usually relevant to glial or thyroid tissues (2). Salivary gland choristomas (SGC) in the cheek, middle ear, neck, jaw, thyroid gland, pituitary gland, mediastinal lymph nodes, breast, anterior chest wall, oesophagus, duodenum, jejunum, rectum and amygdala have been reported (3).en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCerrahien_US
dc.titleSalivary gland choristoma of the larynxen_US
dc.typeletteren_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.identifier.volume34en_US
dc.identifier.issue3en_US
dc.identifier.startpage288en_US
dc.identifier.endpage289en_US
dc.ri.editoaen_US
dc.relation.journalBalkan Medical Journalen_US
dc.relation.publicationcategoryDiğeren_US


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