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Inflammatory myofibroblastic tumor as a second neoplasm after Wilms tumor.
Ortiz, Michael V; Rossi, Christopher T; Hill, D Ashley; Guzzetta, Phillip C; Qureshi, Faisal; Dome, Jeffrey S.
Afiliação
  • Ortiz MV; Division of Oncology, Children's National Health System, Washington, District of Columbia.
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 / 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

Texto completo: 1 Coleções: 01-internacional Base 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