dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorValera, E. T.
dc.creatorSerafini, L. N.
dc.creatorMachado, H. R.
dc.creatorTone, L. G.
dc.date.accessioned2016-01-24T12:33:42Z
dc.date.accessioned2022-10-07T21:39:05Z
dc.date.available2016-01-24T12:33:42Z
dc.date.available2022-10-07T21:39:05Z
dc.date.created2016-01-24T12:33:42Z
dc.date.issued2003-02-01
dc.identifierChilds Nervous System. New York: Springer-verlag, v. 19, n. 2, p. 86-90, 2003.
dc.identifier0256-7040
dc.identifierhttp://repositorio.unifesp.br/handle/11600/27128
dc.identifier10.1007/s00381-002-0704-y
dc.identifierWOS:000181659000003
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4030867
dc.description.abstractIntroduction: Low-grade astrocytomas constitute the majority of pediatric central nervous system neoplasms. Gross total resection is desirable as the initial therapeutic approach and is curative in most cases. in the past, radiation therapy was often recommended for patients in whom complete resection was not achieved, although there are special concerns about secondary malignancy and cognitive impairment. There has been increasing interest in the use of chemotherapy to treat these tumors, but appropriate indications still need to be defined. Case reports: the use of neoadjuvant chemotherapy to ease surgical resection in two children with inoperable pilocytic astrocytomas who presented with extrinsic compression of mesencephalic structures is described. Discussion: This paper also emphasizes and discusses the therapeutic approach for very selected cases of low-grade gliomas in children presenting with inoperable giant lesions, in whom the use of chemotherapy may be considered initially.
dc.languageeng
dc.publisherSpringer
dc.relationChilds Nervous System
dc.rightshttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dc.rightsAcesso restrito
dc.subjectlow-grade gliomas
dc.subjectChildren
dc.subjectchemotherapy
dc.subjectsurgical resection
dc.titleComplete surgical resection in children with low-grade astrocytomas after neoadjuvant chemotherapy
dc.typeArtigo


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