Desmoid-type fibromatosis in a boy with Down syndrome

Pediatr Int. 2017 May;59(5):624-626. doi: 10.1111/ped.13241. Epub 2017 Apr 18.

Abstract

Patients with Down syndrome (DS) have a markedly higher incidence of childhood leukemia, but a lower incidence of most solid tumors, compared with age-matched euploid individuals. Trisomy 21 might be protective against tumorigenesis because of several tumor suppressive mechanisms. Desmoid-type fibromatosis (DF) is a rare monoclonal, fibroblastic proliferation characterized by a variable clinical course. In recent reports, almost all cases of DF involved genomic alterations associated with activation of the Wnt/β-catenin pathway. Here, we report the case of a boy with DS who developed DF without activation of the Wnt/β-catenin pathway. To the best of our knowledge, this is the first case of DS involving DF.

Keywords: Down syndrome; desmoid-type fibromatosis.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Desmoid Tumors / complications
  • Desmoid Tumors / diagnosis*
  • Down Syndrome / complications*
  • Humans
  • Male
  • Thoracic Neoplasms / complications
  • Thoracic Neoplasms / diagnosis*