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EMJ-Emirates Medical Journal. 2006; 24 (2): 151-153
em Inglês | IMEMR | ID: emr-76591

RESUMO

Congenital mesoblastic nephroma [CMN] is a very rare tumour of early infancy with 80% of the cases being diagnosed within the first month of life. Complete surgical excision is almost always curative. We report two unusual large renal tumours in a 22-month-old boy and a 4-year-old girl who were diagnosed preoperatively as rhabdoid tumour and Wilms' tumour respectively. One of them was subjected unnecessarily to preoperative chemotherapy. Histological evaluation after complete radical excision demonstrated CMN


Assuntos
Humanos , Masculino , Feminino , Neoplasias Renais , Tumor de Wilms , Tumor Rabdoide , Nefroma Mesoblástico/congênito
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