Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases

dc.contributor.authorMahomed, N
dc.contributor.authorNaidoo, J
dc.contributor.authorDlangamandla, S
dc.contributor.authorAndronikou, S
dc.contributor.authorPather, S
dc.contributor.authorPillay, K
dc.date.accessioned2016-04-28T14:17:02Z
dc.date.available2016-04-28T14:17:02Z
dc.date.issued2014
dc.date.updated2016-04-28T14:10:04Z
dc.description.abstractAtypical teratoid/rhabdoid tumour of the central nervous system is a rare, highly aggressive childhood malignancy. The age of presentation is usually <2 years, but this tumour may occur in other age groups. The typical location is the posterior fossa, with supratentorial origin less common. We present two cases of atypical teratoid/rhabdoid tumours, with the suprasellar location of one case proving to be a diagnostic radiological challenge.en_ZA
dc.identifierhttp://dx.doi.org/10.7196/SAJCH.655
dc.identifier.apacitationMahomed, N., Naidoo, J., Dlangamandla, S., Andronikou, S., Pather, S., & Pillay, K. (2014). Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases. <i>South African Journal of Child Health</i>, http://hdl.handle.net/11427/19302en_ZA
dc.identifier.chicagocitationMahomed, N, J Naidoo, S Dlangamandla, S Andronikou, S Pather, and K Pillay "Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases." <i>South African Journal of Child Health</i> (2014) http://hdl.handle.net/11427/19302en_ZA
dc.identifier.citationMahomed, N., Naidoo, J., Dlangamandla, S., Andronikou, S., Pather, S., & Pillay, K. (2014). Atypical teratoid/rhabdoid tumour in a supratentorial location: A report of two cases. South African Journal of Child Health, 8(4), 159-161.en_ZA
dc.identifier.issn1994-3032en_ZA
dc.identifier.ris TY - Journal Article AU - Mahomed, N AU - Naidoo, J AU - Dlangamandla, S AU - Andronikou, S AU - Pather, S AU - Pillay, K AB - Atypical teratoid/rhabdoid tumour of the central nervous system is a rare, highly aggressive childhood malignancy. The age of presentation is usually <2 years, but this tumour may occur in other age groups. The typical location is the posterior fossa, with supratentorial origin less common. We present two cases of atypical teratoid/rhabdoid tumours, with the suprasellar location of one case proving to be a diagnostic radiological challenge. DA - 2014 DB - OpenUCT DP - University of Cape Town J1 - South African Journal of Child Health LK - https://open.uct.ac.za PB - University of Cape Town PY - 2014 SM - 1994-3032 T1 - Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases TI - Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases UR - http://hdl.handle.net/11427/19302 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/19302
dc.identifier.urihttp://www.sajch.org.za/index.php/SAJCH/article/view/655
dc.identifier.vancouvercitationMahomed N, Naidoo J, Dlangamandla S, Andronikou S, Pather S, Pillay K. Atypical teratoid/rhabdoid tumour in a supratentorial location: a report of two cases. South African Journal of Child Health. 2014; http://hdl.handle.net/11427/19302.en_ZA
dc.languageengen_ZA
dc.publisherHealth and Medical Publishing Groupen_ZA
dc.publisher.departmentDivision of Anatomical Pathologyen_ZA
dc.publisher.facultyFaculty of Health Sciencesen_ZA
dc.publisher.institutionUniversity of Cape Town
dc.rightsCreative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_ZA
dc.sourceSouth African Journal of Child Healthen_ZA
dc.source.urihttp://www.sajch.org.za/index.php/SAJCH
dc.subject.otherAtypical teratoid/rhabdoid tumour
dc.subject.otherSupratentorial origin
dc.subject.otherPeripheral rim of restricted diffusion
dc.subject.otherCalcification with blooming on gradient sequence
dc.subject.otherCSF seeding
dc.titleAtypical teratoid/rhabdoid tumour in a supratentorial location: a report of two casesen_ZA
dc.typeJournal Articleen_ZA
uct.type.filetypeText
uct.type.filetypeImage
uct.type.publicationResearchen_ZA
uct.type.resourceArticleen_ZA
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