Pitfalls in the Differential Diagnosis of Renal Tumor in an Adolescent
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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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 |
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 |