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dc.contributor.authorMeshkini, A
dc.contributor.authorVahedi, A
dc.contributor.authorMeshkini, M
dc.contributor.authorAlikhah, H
dc.contributor.authorNaghavi-Behzad, M
dc.date.accessioned2018-08-26T06:04:59Z
dc.date.available2018-08-26T06:04:59Z
dc.date.issued2014
dc.identifier10.4103/1793-5482.131077
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41636
dc.description.abstractMedulloblastoma is common in children as a tumor of midline posterior fossa, which arises from vermis and appears as a homogenously enhancing hyperdense mass on computed tomography scan and is associated with the clinical picture of posterior fossa syndrome. This unique clinic-radiological pattern in considered "typical" medulloblastoma, but medulloblastomas does not follow the typical clinic-radiological pattern in a significant number of children and adult cases. We review here the previous reports of atypical or uncommon features of medulloblastoma and add our very rare atypical cases of medulloblastomas to this list. Medulloblastoma should be considered in all midline posterior fossa tumors, hemisphere and cerebellopontine angle despite having clinical and radiological features suggestive of other tumors. Definitive diagnosis requires histologic confirmation in all cases.
dc.language.isoEnglish
dc.relation.ispartofAsian journal of neurosurgery
dc.titleAtypical medulloblastoma: A case series.
dc.typearticle
dc.citation.volume9
dc.citation.issue1
dc.citation.spage45
dc.citation.epage7
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.4103/1793-5482.131077


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