Inflammatory myofibroblastic tumors following the treatment of malignancy in childhood: case reports

J Pediatr Hematol Oncol. 2014 Mar;36(2):159-62. doi: 10.1097/MPH.0b013e31827e5302.

Abstract

Inflammatory myofibroblastic tumors (IMT) are rare, mostly benign soft tissue tumors. Occurring mainly in children the presentation, clinical features, and diagnostic dilemmas raised are well reported. Here we describe 4 patients diagnosed with IMT after the treatment of childhood cancer, and review the literature regarding IMT and malignancy. Discussing them in this context raises clinical questions; Are these tumors incidental or a consequence of treatment? Are they more common than we think and are any miss-diagnosed as tumor recurrence? This paper aims to raise awareness of IMT as diagnostic possibilities after treatment for childhood malignancies.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Female
  • Granuloma, Plasma Cell / diagnosis*
  • Granuloma, Plasma Cell / etiology*
  • Humans
  • Male
  • Neoplasms / therapy*