4.3 Article

Malignant round cell tumor of bone with EWSR1-NFATC2 gene fusion

Journal

VIRCHOWS ARCHIV
Volume 465, Issue 2, Pages 233-239

Publisher

SPRINGER
DOI: 10.1007/s00428-014-1613-7

Keywords

EWSR1-NFATc2 fusion gene; EWSR1; Ewing's sarcoma; Osteosarcoma

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Funding

  1. Intramural NIH HHS [Z99 CA999999] Funding Source: Medline

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Gene rearrangements involving the Ewing sarcoma breakpoint region 1 (EWSR1) gene are seen in a broad range of sarcomas and some nonmesenchymal neoplasms. Ewing sarcoma is molecularly defined by a fusion of the EWSR1 gene (or rarely the related FUS gene) to a member of the E26 transformation-specific (ETS) family of transcription factors, frequently the EWSR1-FLI1 fusion. More recently, EWSR1 gene fusion to non-ETS family members, including the nuclear factor of activated T cells, cytoplasmic, calcineurin-dependent 2 (NFATC2) gene, has been reported in a histological variant of Ewing sarcoma. Here, we report a malignant round cell tumor of bone with an EWSR1-NFATC2 fusion gene. This report builds upon the unusual morphological and clinical presentation of bone neoplasms containing an EWSR1-NFATC2 fusion gene.

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