Inflammatory myofibroblastic tumor as a second neoplasm after Wilms tumor.

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.

journal_name

Pediatr Blood Cancer

journal_title

Pediatric blood & cancer

authors

Ortiz MV,Rossi CT,Hill DA,Guzzetta PC,Qureshi F,Dome JS

doi

10.1002/pbc.25345

subject

Has Abstract

pub_date

2015-06-01 00:00:00

pages

1075-7

issue

6

eissn

1545-5009

issn

1545-5017

journal_volume

62

pub_type

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