NAGIOS: RODERIC FUNCIONANDO

Primitive neuroectodermal kidney tumor

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Primitive neuroectodermal kidney tumor

dc.contributor.author	Segura, Angel
dc.contributor.author	Pérez, José
dc.contributor.author	Reynes Muntaner, Gaspar
dc.contributor.author	Yuste, Ana
dc.contributor.author	Vera Sempere, Francisco José
dc.contributor.author	Petschen, Ignacio
dc.date.accessioned	2020-11-24T09:21:08Z
dc.date.available	2020-11-24T09:21:08Z
dc.date.issued	2005
dc.identifier.citation	Segura, Angel Pérez, José Reynes Muntaner, Gaspar Yuste, Ana Vera Sempere, Francisco José Petschen, Ignacio 2005 Primitive neuroectodermal kidney tumor Medical and Pediatric Oncology 38 2 145 145
dc.identifier.uri	https://hdl.handle.net/10550/76450
dc.description.abstract	To the Editor: Primitive neuroectodermal tumors (PNET) and Ewing sarcoma (ES) belong to a group of neoplasms de®ned by neuroectodermal differentiation and a characteristic cytogenetic translocation, t(11;22) (q24;q12) or gene rearrangements between chromosomes 21 and 22 [1]. They are generally aggressive tumors that present as metastatic disease in nearly 50% of the cases. ES is frequently a bone disease, whereas PNET can occur in bones, soft tissues, or any other site. Renal PNETs are extremely rare, with only a few cases reported [2]. We here record an adult with renal PNET and bone metastases at diagnosis. Because these tumor can also be found in children [3] our experience may therefore be helpful to pediatric oncologists
dc.language.iso	eng
dc.relation.ispartof	Medical and Pediatric Oncology, 2005, vol. 38, num. 2, p. 145-145
dc.subject	Càncer
dc.title	Primitive neuroectodermal kidney tumor
dc.type	journal article	es_ES
dc.date.updated	2020-11-24T09:21:08Z
dc.identifier.doi	10.1002/mpo.1296
dc.identifier.idgrec	141427
dc.rights.accessRights	open access	es_ES