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Urology ; 61(6): 1260, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12809924

ABSTRACT

Congenital mesoblastic nephroma was originally considered to be a benign neoplasm. A more aggressive cellular form, however, that has a close relationship to congenital fibrosarcoma, is widely described. Previous reported sites of metastases are the lungs, heart, brain, and bone. We describe a patient with isolated metastasis to liver and review the management, together with evidence that it may be more appropriate to use a vincristine, ifosfamide, doxorubicin, and etoposide (VIDE) regimen rather than Wilm's tumor-based regimens in those cases for which chemotherapy is indicated.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Kidney Neoplasms/congenital , Kidney Neoplasms/drug therapy , Liver Neoplasms/drug therapy , Liver Neoplasms/metabolism , Nephroma, Mesoblastic/drug therapy , Nephroma, Mesoblastic/secondary , Sarcoma/drug therapy , Doxorubicin/administration & dosage , Etoposide/administration & dosage , Humans , Ifosfamide/administration & dosage , Infant , Kidney Neoplasms/pathology , Liver Neoplasms/congenital , Nephroma, Mesoblastic/congenital , Vincristine/administration & dosage
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