Rhabdomyosarcoma With Epithelioid Features And NSD3::FOXO1 Fusion: Evidence For Reconsideration Of Previously Reported FOXO1::FGFR1 Fusion

Author:

Rakheja Dinesh12ORCID,Park Jason Y.12,Yang Mary S.23,Martinez Diana P.1,Koduru Prasad1,Wilson Kathleen S.1,Garcia Rolando1,Uddin Naseem12

Affiliation:

1. Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA

2. Children’s Health, Dallas, TX, USA

3. Department of Radiology, University of Texas Southwestern Medical Center, Dallas, TX, USA

Abstract

Epithelioid rhabdomyosarcoma is a rare rhabdomyosarcoma variant for which no diagnostic recurrent driver genetic events have been identified. Here we report a rapidly progressive and widely metastatic rhabdomyosarcoma with epithelioid features that arose in the thigh of a male infant. Conventional cytogenetics revealed a t(8;13)(p11.2;q14) translocation. Fluorescence in situ hybridization studies showed rearrangement of FOXO1 and amplification of its 3” end, and rearrangement of NSD3 and amplification of its 5` end. Next generation sequencing identified a NSD3::FOXO1 fusion, which is a previously unreported gene fusion. We also review the historic report of a FOXO1::FGFR1 fusion in a solid variant of alveolar rhabdomyosarcoma and propose that NSD3::FOXO1 fusion may have been the more appropriate interpretation of the data presented in that report.

Funder

Cancer Prevention and Research Institute of Texas

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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