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Review
. 2023 Sep;41(8):704-712.
doi: 10.1080/07357907.2023.2255668. Epub 2023 Sep 6.

Intraosseous Spindle Cell Rhabdomyosarcoma with MEIS1:: NCOA2 Fusion - Case Report with Substantial Clinical Follow-up and Review of the Literature

Affiliations
Review

Intraosseous Spindle Cell Rhabdomyosarcoma with MEIS1:: NCOA2 Fusion - Case Report with Substantial Clinical Follow-up and Review of the Literature

Benjamin F Smith et al. Cancer Invest. 2023 Sep.

Erratum in

  • Correction.
    [No authors listed] [No authors listed] Cancer Invest. 2023 Sep;41(8):750. doi: 10.1080/07357907.2023.2259655. Epub 2023 Oct 31. Cancer Invest. 2023. PMID: 37733418 No abstract available.

Abstract

Spindle cell/sclerosing rhabdomyosarcoma (SSRMS) is a clinicopathologically and molecularly heterogeneous disease. Gene fusions have been identified in intraosseous SSRMS, consisting predominantly of EWSR1/FUS::TFCP2 and MEIS1::NCOA2. The former often follow an aggressive clinical course; there is limited clinical follow-up available for the latter. We report here a new case of the very rare intraosseous SSRMS with MEIS1::NCOA2 gene fusion and include the detailed treatment course and 52 months of clinical follow-up. SSRMS with MEIS1::NCOA2 gene fusion appears biologically distinct from other intraosseous SSRMS, following a course characterized by local recurrence with rare reports of metastasis to date.

Keywords: MEIS1; NCOA2; Rhabdomyosarcoma; bone; gene fusion.

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