6533b851fe1ef96bd12a9a9e

RESEARCH PRODUCT

Primitive neuroectodermal kidney tumor

Ana L. YusteIgnacio PetschenGaspar ReynésFrancisco VeraJosé Francisco PérezÁNgel Segura

subject

Cancer ResearchPathologymedicine.medical_specialtyText miningOncologybusiness.industryPediatrics Perinatology and Child HealthMedicinebusinessCàncerKidney tumor

description

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

10.1002/mpo.1296https://doi.org/10.1002/mpo.1296