A Rare TPM3-NTRK1 fusion in a fetal pelvic mass
Early recognition and characterization of soft tissue tumors is important for proper fetal and maternal care. Here, we present sonographic, fetal and postnatal MRI, and pathological findings of a rare case of congenital NTRK-rearranged malignant spindle cell sarcoma with TPM3-NTRK1 fusion in a male fetus.
Authors
- J Kucera (ORCID: https://orcid.org/0000-0001-6075-9463)
- Lei Shao (ORCID: https://orcid.org/0000-0003-0368-7269)
- Maryam Kazelka (ORCID: https://orcid.org/0009-0000-2222-7781)
- Michael Mcgraw
Institutions
- University of Central Florida (US)
- University of South Florida (US)
- Tampa General Hospital (US)
- Nemours Children's Clinic (US)
Publication Details
- Journal
- Radiology Case Reports
- Published
- 2025-03-15
- DOI
- https://doi.org/10.1016/j.radcr.2025.02.079
- Primary Topic
- Neuroblastoma Research and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00