Inflammatory myofibroblastic tumor as a second neoplasm after Wilms tumor.
Pediatr Blood Cancer
; 62(6): 1075-7, 2015 Jun.
Article
em En
| MEDLINE
| ID: mdl-25504840
ABSTRACT
We report two survivors of Wilms tumor (WT) who developed inflammatory myofibroblastic tumor (IMT). The first patient had IMT in the mainstem bronchus 1 year after WT therapy that included vincristine, dactinomycin, doxorubicin (VDA) and whole lung radiation therapy (XRT). The second patient had IMT in the cecum 7 years after WT therapy consisting of VDA and abdominal XRT. The unlikely co-occurrence of WT and IMT suggests a genetic link between these tumors or that IMT can arise as a complication of cancer therapy. IMT should be considered in WT survivors who develop secondary tumors, especially at unusual sites.
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Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Segunda Neoplasia Primária
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Tumor de Wilms
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Granuloma de Células Plasmáticas
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Neoplasias Renais
Limite:
Child, preschool
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Female
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Humans
Idioma:
En
Revista:
Pediatr Blood Cancer
Assunto da revista:
HEMATOLOGIA
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NEOPLASIAS
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PEDIATRIA
Ano de publicação:
2015
Tipo de documento:
Article