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dc.creatorEspín, Luis
dc.creatorQuispe-Alcocer, Julio
dc.creatorEspín, Gabriela
dc.creatorVillacís-Sandoval, Jorge
dc.creatorCastro-Viteri, Jesús
dc.date2016-12-01
dc.date.accessioned2020-10-07T22:50:16Z
dc.date.available2020-10-07T22:50:16Z
dc.identifierhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/123
dc.identifier10.32457/ijmss.2016.036
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/154224
dc.descriptionExtraosseous Ewing’s sarcoma belongs to the family of neuroectodermal tumors that derive from the neural crest, characteristic of its aggressiveness. Several locations have been described, however, epidural presentation is rare. Prognosis has been improved by new oncological regimens and other therapeutic targets are being studied.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherUniversidad Autónoma de Chileen-US
dc.relationhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/123/119
dc.rightsCopyright (c) 2020 International Journal of Medical and Surgical Sciencesen-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 3 No. 4 (2016): December 2016; 1003-1007en-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 3 Núm. 4 (2016): December 2016; 1003-1007es-ES
dc.source0719-532X
dc.source0719-3904
dc.subjectExtraosseous Ewing’s sarcomaen-US
dc.subjectNeuroectodermal tumorsen-US
dc.titleExtraosseous Ewing’s Sarcoma in Spinal Epidural Spaceen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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