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Sclerosing Epithelioid Fibrosarcoma of the Bone With Rare EWSR1-CREB3L3 Translocation Driving Upregulation of the PI3K/mTOR Signaling Pathway.
Shenoy, Archana; Surrey, Lea; Jain, Payal; Foster, Jessica; Straka, Joshua; Resnick, Adam; Waanders, Angela; Luo, Minjie; Li, Marilyn; Kazahaya, Ken; Bagatell, Rochelle; Wojcik, John; Pogoriler, Jennifer.
Affiliation
  • Shenoy A; University of Florida College of Medicine, Gainesville, Florida.
  • Surrey L; Children's Hospital of Philadelphia, Pathology, Immunology and Laboratory medicine, Philadelphia, Pennsylvania.
  • Jain P; Children's Hospital of Philadelphia, Center for Data Driven Discovery in Biomedicine, Philadelphia, Pennsylvania.
  • Foster J; Children's Hospital of Philadelphia, Division of Oncology, Pediatrics, Philadelphia, Pennsylvania.
  • Straka J; Children's Hospital of Philadelphia, Center for Data Driven Discovery in Biomedicine, Philadelphia, Pennsylvania.
  • Resnick A; Children's Hospital of Philadelphia, Center for Data Driven Discovery in Biomedicine, Philadelphia, Pennsylvania.
  • Waanders A; Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Luo M; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Li M; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Kazahaya K; Children's Hospital of Philadelphia, Department of Clinical Otorhinolaryngology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Bagatell R; Children's Hospital of Philadelphia, Division of Oncology, Pediatrics, Philadelphia, Pennsylvania.
  • Wojcik J; University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
  • Pogoriler J; Children's Hospital of Philadelphia, Pathology, Immunology and Laboratory medicine, Philadelphia, Pennsylvania.
Pediatr Dev Pathol ; 22(6): 594-598, 2019.
Article in En | MEDLINE | ID: mdl-31335288
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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Mandibular Neoplasms / Biomarkers, Tumor / Oncogene Proteins, Fusion / Phosphatidylinositol 3-Kinase / TOR Serine-Threonine Kinases / Fibrosarcoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Pediatr Dev Pathol Journal subject: PATOLOGIA / PEDIATRIA Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Mandibular Neoplasms / Biomarkers, Tumor / Oncogene Proteins, Fusion / Phosphatidylinositol 3-Kinase / TOR Serine-Threonine Kinases / Fibrosarcoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Pediatr Dev Pathol Journal subject: PATOLOGIA / PEDIATRIA Year: 2019 Type: Article