| Literature DB >> 31335288 |
Archana Shenoy1, Lea Surrey2, Payal Jain3, Jessica Foster4, Joshua Straka3, Adam Resnick3, Angela Waanders5, Minjie Luo6, Marilyn Li6, Ken Kazahaya7, Rochelle Bagatell4, John Wojcik8, Jennifer Pogoriler2.
Abstract
Sclerosing epithelioid fibrosarcoma (SEF) is an uncommon neoplasm that rarely presents in bone. It is characterized by epithelioid cells arranged in nests and single-file cords within a sclerotic stromal background which may mimic neoplastic bone. SEF harbors an EWSR1 translocation, which may complicate its distinction from Ewing sarcoma in cases with histomorphologic overlap. We present a diagnostically challenging case of SEF in the mandible of a 16-year-old girl. Our experience highlights the lack of specificity of traditional morphology and EWSR1 break-apart fluorescent in situ hybridization. Open-ended RNA-based fusion gene testing coupled with MUC4 immunohistochemistry aided the eventual diagnosis in this case. Herein, we report the third case of SEF with EWSR1-CREB3L3 translocation and show that this fusion leads to aberrant upregulation of the phosphoinositide 3-kinase/mammalian target of rapamycin signaling pathway in heterologous cell models.Entities:
Keywords: EWSR1 translocation; Ewing sarcoma; bone tumors; molecular oncology; sarcoma; sclerosing epithelioid fibrosarcoma
Mesh:
Substances:
Year: 2019 PMID: 31335288 DOI: 10.1177/1093526619864230
Source DB: PubMed Journal: Pediatr Dev Pathol ISSN: 1093-5266