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dc.contributor.authorMalheiros, SMF
dc.contributor.authorFranco, CMR
dc.contributor.authorStavale, J. N.
dc.contributor.authorSantos, A. J.
dc.contributor.authorBorges, LRR
dc.contributor.authorPelaez, M. P.
dc.contributor.authorFerraz, FAP
dc.contributor.authorGabbai, Alberto Alain [UNIFESP]
dc.date.accessioned2016-01-24T12:33:37Z
dc.date.available2016-01-24T12:33:37Z
dc.date.issued2002-12-01
dc.identifierhttp://dx.doi.org/10.1023/A:1021178518361
dc.identifier.citationJournal of Neuro-oncology. Dordrecht: Kluwer Academic Publ, v. 60, n. 3, p. 247-253, 2002.
dc.identifier.issn0167-594X
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/27065
dc.description.abstractWe retrospectively reviewed 15 adult patients (11 males, median age 34 years; range 23-48) who had been treated and followed in our Institution since 1991 from the time of diagnosis until death or last follow-up in December 2001. Headache was the most frequent symptom (93%). the tumor was hemispheric in 11 patients. Complete resection was achieved in eight. CSF in 12 patients and craniospinal MRI in 6 did not show metastatic disease. Two patients refused adjuvant treatment and died with progressive disease. Thirteen patients received adjuvant craniospinal radiotherapy and 11 systemic chemotherapy. After initial treatment only 2 of the 13 patients relapsed in the posterior fossa. Recurrence was probably related to sub-optimal radiotherapy planning: inadequate low dose in the posterior fossa (37.5 Gy) and long delay in initiating treatment. Two of the 13 patients that received adjuvant treatment died: one from meningitis, and one from recurrent disease. Eleven patients remained alive, and disease-free with Karnofsky performance status ranging 80-100. the median overall survival was not reached after a median follow-up of 5.6 years (range 0.7-10.8 years). Estimated 1-, 5- and 10-year overall survival rates were 86.7%, 72.7%, and 72.7%, respectively. Adult medulloblastoma was predominant in males and the majority of patients had hemispheric tumors. Long-term survival was not uncommon. Although chemotherapy may be useful and well tolerated, radiotherapy remains the mainstay adjuvant treatment as suggested by our two recurrences associated with a delay or inadequate dose.en
dc.format.extent247-253
dc.language.isoeng
dc.publisherKluwer Academic Publ
dc.relation.ispartofJournal of Neuro-oncology
dc.rightsAcesso restrito
dc.subjectmedulloblastomaen
dc.subjectsurgeryen
dc.subjectchemotherapyen
dc.subjectradiation therapyen
dc.subjectadulten
dc.subjectdesmoplasticen
dc.titleMedulloblastoma in adults: a series from Brazilen
dc.typeArtigo
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationUniversidade Federal de São Paulo, Dept Neurol, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, Dept Neurosurg, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, Dept Pathol, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Neurol, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Neurosurg, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Pathol, Escola Paulista Med, BR-04023900 São Paulo, Brazil
dc.identifier.doi10.1023/A:1021178518361
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000179312400005


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