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dc.contributor.authorBelsuzarri, Telmo A B
dc.contributor.authorAraujo, João F M
dc.contributor.authorCatanoce, Aguinaldo P
dc.contributor.authorNeves, Maick W F
dc.contributor.authorSola, Rodrigo A S
dc.contributor.authorNavarro, Juliano N
dc.contributor.authorBrito, Leandro G
dc.contributor.authorSilva Junior, Nilton R
dc.contributor.authorPontelli, Luis Otavio C
dc.contributor.authorMattos, Luiz Gustavo A
dc.contributor.authorGonçales, Tiago F
dc.contributor.authorZeviani, Wolnei M
dc.contributor.authorMarques, Renata M B
dc.date.accessioned2025-04-24T17:30:48Z
dc.date.available2025-04-24T17:30:48Z
dc.date.issued2015
dc.identifier.urihttp://repositorio.sis.puc-campinas.edu.br/xmlui/handle/123456789/17840
dc.description.abstractGlioblastoma multiforme (GBM) is the most common glial tumor of the brain system; nevertheless, the giant cell (GC) subtype is uncommon. Recent reviews report for an incidence of 1% in adults and 3% in children. The GCs usually have a better prognosis than GBM and also an increasing long-term survival rate. It is known that the diagnosis of this tumor is due to its histological findings and patterns, such as the unusual increased number of giant cells. Unfortunately, due to its rarity, the immunohistochemical and cytogenetical analysis of this tumor is not well known. Some authors also suggest that there are few subtypes of GCs and their patterns of aggressiveness could be due to cytogenetical markers. It is recognized that maximum safe resection treatment and adjuvant radiotherapy can improve survival rate (5-13 months) similar to GBM patients.pt_BR
dc.language.isoInglêspt_BR
dc.publisherRare Tumorspt_BR
dc.rightsAcesso abertopt_BR
dc.subjectGeneticpt_BR
dc.subjectGiant cell glioblastomapt_BR
dc.subjectGlioblastoma multiformept_BR
dc.subjectImmunohistochemicalpt_BR
dc.subjectLong-term survival.pt_BR
dc.titleGiant cells glioblastoma: case report and pathological analysis from this uncommon subtype of gliomapt_BR
dc.typeArtigopt_BR
dc.contributor.institutionPontifícia Universidade Católica de Campinas (PUC-Campinas)pt_BR
dc.identifier.doihttps://doi.org/10.4081/rt.2015.5634pt_BR
puc.advisorLattes9848550164557926


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