Sclerosing Epithelioid Fibrosarcoma of the Bone With Rare EWSR1-CREB3L3 Translocation Driving Upregulation of the PI3K/mTOR Signaling Pathway.
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.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Translocation, Genetic
/
Mandibular Neoplasms
/
Biomarkers, Tumor
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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