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dc.contributor.authorTunca, F
dc.contributor.authorBasar, Y
dc.contributor.authorKapran, Y
dc.contributor.authorTanakol, R
dc.contributor.authorTerzioglu, T
dc.contributor.authorGenc, FA
dc.contributor.authorAksoy, M
dc.date.accessioned2021-03-06T20:59:20Z
dc.date.available2021-03-06T20:59:20Z
dc.date.issued2003
dc.identifier.citationGenc F., Aksoy M., Kapran Y., Tunca F., Tanakol R., Basar Y., Terzioglu T., "Adrenal neuroblastoma in an adult: Report of a case", SURGERY TODAY, cilt.33, ss.879-881, 2003
dc.identifier.issn0941-1291
dc.identifier.otherav_fcbfb063-8166-47a2-b391-cca903866f35
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/165392
dc.identifier.urihttps://doi.org/10.1007/s00595-003-2622-3
dc.description.abstractNeuroblastomas comprise a major part of adrenal tumors in children. However, they are seldom reported in adults. In this report we present the case of a 30-year-old woman who was operated on for an incidentaloma. Following an adrenalectomy, she was put on a chemoradiotherapy regimen. A histopathologic assessment of the specimen revealed Homer-Wright rosettes against a background of fibrillary matrix, which indicated a diagnosis of a neuroblastoma. In spite of a low incidence in adulthood, it should be emphasized that all adrenal tumors without any particular characteristics may be a neuroblastoma, which tends to show a very poor prognosis. Hence, such patients should undergo postoperative chemoradiotherapy, which may improve both the remission rates and survival.
dc.language.isoeng
dc.subjectTıp
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleAdrenal neuroblastoma in an adult: Report of a case
dc.typeMakale
dc.relation.journalSURGERY TODAY
dc.contributor.department, ,
dc.identifier.volume33
dc.identifier.issue11
dc.identifier.startpage879
dc.identifier.endpage881
dc.contributor.firstauthorID169768


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