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.
Palavras-chave
Texto completo:
1
Bases de dados:
MEDLINE
Assunto principal:
Segunda Neoplasia Primária
/
Tumor de Wilms
/
Granuloma de Células Plasmáticas
/
Neoplasias Renais
Limite:
Child, preschool
/
Female
/
Humans
Idioma:
En
Revista:
Pediatr Blood Cancer
Assunto da revista:
HEMATOLOGIA
/
NEOPLASIAS
/
PEDIATRIA
Ano de publicação:
2015
Tipo de documento:
Article