Uterine Sarcoma With FGFR1-TACC1 Gene Fusion: A Case Report and Review of the Literature

Int J Gynecol Pathol. 2022 Nov 1;41(6):588-592. doi: 10.1097/PGP.0000000000000846. Epub 2021 Dec 1.

Abstract

With the growing availability of RNA sequencing technology in the pathology laboratory, new gene fusion-associated malignancies are increasingly being characterized. In this article, we describe the second ever reported case of a uterine sarcoma harboring a FGFR1-TACC1 gene fusion. The patient, a 53-yr-old perimenopausal woman, was found to have a 6 cm mass spanning the lower uterine segment and endocervix. Histologically, this was a spindle cell neoplasm with coagulative necrosis, moderate cytologic atypia, and increased mitotic activity. By immunohistochemistry, the neoplastic cells coexpressed CD34 and S100, and lacked smooth muscle marker expression. RNA sequencing revealed the presence of a FGFR1-TACC1 gene fusion. This report provides further evidence to suggest that FGFR1-TACC1 may be a recurrent fusion in a subset of uterine sarcomas. RNA sequencing using a panel that includes FGFR-TACC family fusions should be considered for uterine sarcomas that do not fit conventional diagnostic criteria, particularly as tumors with these fusions may be amenable to targeted therapy.

Publication types

  • Review
  • Case Reports

MeSH terms

  • Female
  • Fetal Proteins / genetics
  • Gene Fusion
  • Humans
  • Immunohistochemistry
  • Microtubule-Associated Proteins / genetics
  • Nuclear Proteins / genetics
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics
  • Sarcoma* / diagnosis
  • Sarcoma* / genetics
  • Sarcoma* / metabolism
  • Soft Tissue Neoplasms* / pathology
  • Uterine Neoplasms* / chemistry
  • Uterine Neoplasms* / diagnosis
  • Uterine Neoplasms* / genetics

Substances

  • TACC1 protein, human
  • Fetal Proteins
  • Microtubule-Associated Proteins
  • Nuclear Proteins
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1