| Literature DB >> 12571469 |
Megan K Dishop1, Brad W Warner, Louis P Dehner, Vesna M Kriss, Martha F Greenwood, John D Geil, Jeffrey A Moscow.
Abstract
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.Entities:
Mesh:
Year: 2003 PMID: 12571469 DOI: 10.1097/00043426-200302000-00014
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289