Pitfalls in the Differential Diagnosis of Renal Tumor in an Adolescent


Autoria(s): VALERA, Elvis Terci; BRASSESCO, Maria Sol; CORTEZ, Maria Anglica Abdalla de Freitas; QUEIROZ, Rosane Gomes; CASTRO-GAMERO, Angel Mauricio; BARROS, Marcus Vinicius de Castro; VICENTE, Yvone Avalloni; TUCCI JUNIOR, Silvio; SCRIDELI, Carlos Alberto; TONE, Luiz Gonzaga
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

The differential diagnosis of renal tumors, particularly in adolescents, may be challenging. We describe an 11-year-old female with a primary intra-renal mass. Initial differential diagnoses included primitive neuroectodermal tumor (PNET), desmoplastic small round cell tumor (DSRCT), and Wilms Turner (WT). Extensive pathologic and molecular analysis on initial and relapsed tumor samples confirmed WT. The EWS-WTI and EWS-FL11 rearrange-merits, distinctive of DSRCT and PNET were negative. The differential diagnosis on monophasic blastemal WT may be complex. Primary renal DSRCT and MET have been rarely described. Nevertheless, molecular confirmation for these rare conditions may be necessary in selected cases. Pediatr Blood Cancer 2010;54:3 19-321. (C) 2009 Wiley-Liss, Inc.

Identificador

PEDIATRIC BLOOD & CANCER, v.54, n.2, p.319-321, 2010

1545-5009

http://producao.usp.br/handle/BDPI/24868

10.1002/pbc.22289

http://dx.doi.org/10.1002/pbc.22289

Idioma(s)

eng

Publicador

WILEY-LISS

Relação

Pediatric Blood & Cancer

Direitos

restrictedAccess

Copyright WILEY-LISS

Palavras-Chave #cancer genetics #cytogenetics #molecular genetics #pathology #renal tumors #wilms tumor #ROUND-CELL TUMOR #WILMS-TUMOR #FEATURES #CHILDHOOD #KIDNEY #Oncology #Hematology #Pediatrics
Tipo

article

original article

publishedVersion