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dc.contributor.authorInci, Ender
dc.contributor.authorKORKUT, N
dc.contributor.authorEREM, M
dc.contributor.authorKALEKOGLU, N
dc.date.accessioned2021-03-02T20:07:56Z
dc.date.available2021-03-02T20:07:56Z
dc.date.issued2004
dc.identifier.citationInci E., KORKUT N., EREM M., KALEKOGLU N., "Alveolar soft part sarcoma", HNO, cilt.52, sa.2, ss.145-148, 2004
dc.identifier.issn0017-6192
dc.identifier.othervv_1032021
dc.identifier.otherav_006c1a8c-b032-4af4-bbed-637e624f9c23
dc.identifier.urihttp://hdl.handle.net/20.500.12627/6267
dc.identifier.urihttps://doi.org/10.1007/s00106-003-0872-4
dc.description.abstractAlveolar soft part sarcoma is a malignant soft part tumor the etiology of which has not yet been clarified. Histopathological examinations show an alveolar or pseudoglandular pattern. PAS-positive, diastase resistant intraplasmic inclusion bodies are characteristic for this tumor which occurs in the head and neck region; mainly the tongue and the orbita. Primary therapy includes total resection which can later be combined with radiotherapy or chemotherapy. The present study involves a 17 year old patient. We totally removed the tumor and then used radiotherapy. The postoperative examinations over 3 years showed neither local recurrence nor distant metastases.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKulak Burun Boğaz
dc.subjectKULAK BURUN BOĞAZ
dc.titleAlveolar soft part sarcoma
dc.typeMakale
dc.relation.journalHNO
dc.contributor.department, ,
dc.identifier.volume52
dc.identifier.issue2
dc.identifier.startpage145
dc.identifier.endpage148
dc.contributor.firstauthorID58142


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