A Giant Ureteral Inflammatory Myofibroblastic Tumor in a 4-Year-Old Child: A Case Report and Review of the Literature

Urology. 2022 Jul:165:312-315. doi: 10.1016/j.urology.2022.01.028. Epub 2022 Jan 31.

Abstract

Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm of children and young adults. It consists of myofibroblastic cells of borderline malignancy admixed with inflammatory cells. According to the WHO classification, of tumors, it is a soft-tissue tumor with an intermediate malignant potential. It may arise within numerous organs. Ureteral location is exceedingly rare. We report the exceptional case of a 4-year-old boy presenting with a giant right ureteral IMT removed during a nephroureterectomy. Histology and immunohistochemistry confirmed the diagnosis of an IMT with Anaplastic Lymphoma Kinase 1 expression. A 7 months follow-up showed no recurrence or distant metastasis. We also reviewed the literature for similar cases of pediatric ureteral IMT.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child
  • Child, Preschool
  • Granuloma, Plasma Cell* / diagnostic imaging
  • Granuloma, Plasma Cell* / surgery
  • Humans
  • Immunohistochemistry
  • Male
  • Nephroureterectomy
  • Ureter* / pathology
  • Ureter* / surgery
  • Young Adult