Primitive neuroectodermal kidney tumor
NAGIOS: RODERIC FUNCIONANDO

Primitive neuroectodermal kidney tumor

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Primitive neuroectodermal kidney tumor

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Segura, Angel; Pérez, José; Reynes Muntaner, Gaspar; Yuste, Ana; Vera Sempere, Francisco José Perfil; Petschen, Ignacio
This document is a artículoDate2005
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

    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
https://doi.org/10.1002/mpo.1296

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