Myoepithelial tumor with EWSR1-PBX3 fusion and rearrangement in rib and soft tissue: a rare case report

Myoepithelial tumor (MET) is rare and heterogeneous. We present a case of a MET occurring in the rib and the soft tissue surrounding it. Further, the tumor has been reported to contain both <i>EWSR1-PBX3</i> fusion and rearrangement. A 52-year-old male presented with worsening low back pain. Imaging showed osteolytic destruction of the left twelfth rib accompanied by a soft-tissue mass. Histopathology revealed spindle and oval tumor cells with mild atypia. The entity was positive for S-100, EMA, SMA and calponin by immunohistochemistry but negative for cytokeratin. Testing through next-generation sequencing (NGS) verified the presence of the <i>EWSR1-PBX3</i> fusion and rearrangement. After surgical resection and post-operative radiotherapy, the patient remained disease-free for 2 years. The presence of <i>EWSR1-PBX3</i> fusion and rearrangement in METs of bone and soft tissue is diagnostically significant. It is critical that molecular testing should be performed by clinicians, notably when distinguishing it from synovial sarcoma and other closely related entities.

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Journal
Frontiers in Oncology
Published
2026-02-27
DOI
https://doi.org/10.3389/fonc.2026.1776713
Primary Topic
Sarcoma Diagnosis and Treatment
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article

Myoepithelial tumor with EWSR1-PBX3 fusion and rearrangement in rib and soft tissue: a rare case report

Tingting Zhao, Junting Yang, Jie Liu, Yangcan Li et al.
Frontiers in Oncology
Sarcoma Diagnosis and Treatment
article

Myoepithelial tumor with EWSR1-PBX3 fusion and rearrangement in rib and soft tissue: a rare case report

Tingting Zhao, Junting Yang, Jie Liu, Yangcan Li, Boxiukang Zhang, Shuwei Yu
article en

Abstract

Myoepithelial tumor (MET) is rare and heterogeneous. We present a case of a MET occurring in the rib and the soft tissue surrounding it. Further, the tumor has been reported to contain both <i>EWSR1-PBX3</i> fusion and rearrangement. A 52-year-old male presented with worsening low back pain. Imaging showed osteolytic destruction of the left twelfth rib accompanied by a soft-tissue mass. Histopathology revealed spindle and oval tumor cells with mild atypia. The entity was positive for S-100, EMA, SMA and calponin by immunohistochemistry but negative for cytokeratin. Testing through next-generation sequencing (NGS) verified the presence of the <i>EWSR1-PBX3</i> fusion and rearrangement. After surgical resection and post-operative radiotherapy, the patient remained disease-free for 2 years. The presence of <i>EWSR1-PBX3</i> fusion and rearrangement in METs of bone and soft tissue is diagnostically significant. It is critical that molecular testing should be performed by clinicians, notably when distinguishing it from synovial sarcoma and other closely related entities.

Frontiers in OncologyVol. 16
Xizang Minzu University (CN), Yuhuangding Hospital (CN), The First Hospital of Changsha (CN)
Good health and well-being
Openalex Percentile: Top 41%
Sarcoma Diagnosis and Treatment
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