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J Pediatr Hematol Oncol ; 25(2): 153-8, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12571469

RESUMO

Inflammatory myofibroblastic tumor (IMT) is a tumor composed of myofibroblasts and a mixed inflammatory infiltrate that rarely undergoes malignant transformation. The authors present the case of a 7-year-old boy with an abdominal mass diagnosed as IMT with malignant transformation. The tumor recurred twice after attempts at resection and was initially treated with vincristine and etoposide. After a third recurrence and incomplete resection, he was treated with cisplatin, Adriamycin, and methotrexate. He is disease-free after 2 years, representing successful combined surgery and chemotherapy in the treatment of malignant IMT. The use of chemotherapy for aggressive myofibroblastic tumors is reviewed.


Assuntos
Neoplasias Abdominais/tratamento farmacológico , Neoplasias Abdominais/cirurgia , Recidiva Local de Neoplasia/tratamento farmacológico , Recidiva Local de Neoplasia/cirurgia , Neoplasias de Tecido Muscular/tratamento farmacológico , Neoplasias de Tecido Muscular/cirurgia , Neoplasias Abdominais/patologia , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Transformação Celular Neoplásica , Criança , Humanos , Inflamação , Masculino , Neoplasias de Tecido Muscular/patologia , Tomografia Computadorizada por Raios X , Resultado do Tratamento
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