Introduction: Here, we report the first case of a soft tissue tumor with a fusion.
Case Presentation: The patient was an 11-year-old female presenting with a 5 cm intramuscular mass in the lower leg. Microscopic examination revealed a mitotically active spindle cell lesion with monomorphic and moderately atypical cells growing in a patternless pattern with the presence of stromal and perivascular keloidal collagen with focal immunoreactivity for smooth muscle actin and S100; negative stains included cytokeratins, CD34, and caldesmon. Whole genome and RNA sequencing detected a chromosome 3 inversion and a resultant fusion as well as a CDKN2A homozygous deletion. The patient was treated with neoadjuvant chemoradiotherapy with only minimal response and the tumor was excised surgically. There was no evidence of disease progression at 4 months.
Conclusion: This is the first case of a soft tissue tumor harboring a fusion with histological features in keeping with previous cases of and other kinase fusion soft tissue tumors.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11521462 | PMC |
http://dx.doi.org/10.1159/000540581 | DOI Listing |
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