FOS and FOSB Immunohistochemistry and Molecular Testing Reveal Novel Patterns in Proliferative Fasciitis and Myositis, FOSB Rearrangement in Proliferative Funiculitis, and FOSL1::RELA Fusion in Pediatric Proliferative Fasciitis
Proliferative fasciitis (PFA) and proliferative myositis (PM) are related benign neoplasms that show large ganglion-like neoplastic cells and harbor recurrent FOS fusions. Proliferative funiculitis (PFU) is a benign mesenchymal lesion of the spermatic cord, with small ganglion-like cells and unknown etiology. Ischemic fasciitis (IFA) is a possibly reactive lesion that shows cytomorphologic overlap with PFA/PM. Here, we assessed FOS and FOSB immunohistochemistry (IHC) in PFA (adult and pediatric), PM, PFU, and IFA. Diffuse nuclear FOS expression was detected in adult PFA (15/26 cases; 58%) and PM (6/10; 60%), while FOSB was consistently negative (19 adult PFA, 5 PM). FOS FISH demonstrated rearrangement in only 4 of 12 tested adult PFA/PM, all of which were FOS-positive by IHC. A FOS fusion (FOS::TSHZ2) was detected in only 1 of 9 adult PFA/PM (11%) tested by RNA sequencing (RNAseq); 5 tumors without detected FOS fusions by RNAseq were FOS-positive by IHC. The pediatric PFA lacked expression of FOS (all 9 tumors) and FOSB (4 tested tumors) by IHC. Compared with FOS-positive PFA/PM, pediatric PFA and adult FOS-negative PFA/PM were more frequently cellular, and pediatric tumors were less infiltrative. DNA sequencing demonstrated FOSL1::RELA fusions in 2 of 5 tested pediatric PFAs, both in infants. Six of 18 PFU (33%) expressed FOS and/or FOSB by IHC. FISH demonstrated FOSB rearrangement in 1 of 6 PFU, while all 6 tested PFU were negative for FOS rearrangement. Nine of 20 IFA (45%) expressed FOS and/or FOSB; 2 tested tumors were negative for FOS or FOSB fusions by RNAseq. We conclude that about 60% of adult PFA/PM strongly express FOS, and 5 of these tumors were proven to harbor FOS rearrangements, including a novel FOS::TSHZ2 fusion. Some PFU and pediatric PFA harbored alterations in related genes FOSB and FOSL1, respectively. RNAseq and FISH might have imperfect sensitivity for FOS alterations in PFA/PM, likely due to the low relative neoplastic cell content in these tumor types.
Authors
- Linda Magnusson (ORCID: https://orcid.org/0000-0002-4242-3461)
- Sanhong Yu
- Fleur Cordier (ORCID: https://orcid.org/0000-0003-0876-3398)
- F. Haglund de Flon
- Siebe Loontiens (ORCID: https://orcid.org/0000-0002-4602-4580)
- Joni Van der Meulen (ORCID: https://orcid.org/0000-0002-1916-2769)
- Liesbeth Ferdinande (ORCID: https://orcid.org/0009-0008-4030-761X)
- Esther Baranov
- Jo Van Dorpe (ORCID: https://orcid.org/0000-0002-0783-4484)
- David Creytens (ORCID: https://orcid.org/0000-0002-6064-1673)
- Fredrik Mertens
- Christopher D.M. Fletcher
- Igor Odintsov
- David J. Papke
Institutions
- Brigham and Women's Hospital (US)
- Harvard University (US)
- Lund University (SE)
- Ghent University Hospital (BE)
- Research Foundation - Flanders (BE)
- Karolinska Institutet (SE)
- Yale University (US)
- Cancer Research Institute Ghent (BE)
- University of Pennsylvania (US)
Publication Details
- Journal
- The American Journal of Surgical Pathology
- Published
- 2026-03-26
- DOI
- https://doi.org/10.1097/pas.0000000000002540
- Primary Topic
- Soft tissue tumor case studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00