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SS18-SSX Expression and Clinicopathologic Profiles in a Contemporary Cohort of Primary Paratesticular Synovial Sarcoma: A Series of Fourteen Patients.
- Source :
-
The American journal of surgical pathology [Am J Surg Pathol] 2025 Jan 01; Vol. 49 (1), pp. 11-19. Date of Electronic Publication: 2024 Oct 25. - Publication Year :
- 2025
-
Abstract
- Synovial sarcoma (SS) is a rare genitourinary malignancy with a specific SS18::SSX 1/2 gene fusion in majority of the instances. The paratesticular location of this neoplasm is extremely rare and only 4 cases are reported in the literature. Herein, we describe the clinicopathologic features and molecular profile of paratesticular SS in the largest case series to date and to the best of our knowledge, and the only series to use novel SS18-SSX antibody for immunohistochemistry. Clinicopathologic, immunohistochemical (IHC), molecular, treatment, and follow-up data of the patients were analyzed. There were 14 patients, ranging from 15 to 47 years (mean: 30 y). The tumor size ranged from 4 to 15 cm. The tumors were unilateral, solid, and homogeneous tan-white with monomorphic spindle cell histology. All 14 tumors expressed SS18-SSX and TLE1 IHC and harbored SS18 rearrangement. In addition, the tumor with multifocal SS18-SSX expression had lower break-apart signals in the FISH assay (38% of the tumor cells; range: 29% to 85%). Radical orchiectomy was performed in all 14 patients and adjuvant chemotherapy was administered in 9 patients. Follow-up was available in 9 patients. The follow-up duration ranged from 5 to 24 months (median=10 mo). Four patients died of metastatic disease (range: 5 to 16 mo) and 2 patients who are alive had metastatic disease at the last follow-up. Based on our experience with the largest series to date and aggregate of the published data, paratesticular SS has a poor prognosis despite aggressive therapy. Owing to its rarity, the differential diagnosis is wide and requires a systematic approach for ruling out key morphologic mimics aided with SS18-SSX IHC and molecular confirmation because this distinction carries important therapeutic and prognostic implications. Due to the excellent concordance of SS18-SSX IHC results with FISH results as observed in our study, we would like to suggest inclusion of SS18-SSX in the diagnostic immunohistochemistry panel of all spindle cell sarcomas where synovial sarcoma is considered as a morphologic differential. SS18-SSX-positive staining may be used as a surrogate for FISH assay in a resource-limited setting where molecular assay is not available. Furthermore, IHC has a fairly shorter turn-around-time, is less complex, and of low cost.<br />Competing Interests: Conflicts of Interest and Source of Funding: The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article.<br /> (Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)
- Subjects :
- Humans
Male
Middle Aged
Adult
Adolescent
Young Adult
In Situ Hybridization, Fluorescence
Gene Rearrangement
Repressor Proteins genetics
Repressor Proteins analysis
Treatment Outcome
Co-Repressor Proteins
Orchiectomy
Predictive Value of Tests
Time Factors
Neoplasm Proteins
Proto-Oncogene Proteins
Sarcoma, Synovial pathology
Sarcoma, Synovial genetics
Sarcoma, Synovial chemistry
Sarcoma, Synovial mortality
Sarcoma, Synovial therapy
Biomarkers, Tumor analysis
Biomarkers, Tumor genetics
Immunohistochemistry
Oncogene Proteins, Fusion genetics
Testicular Neoplasms pathology
Testicular Neoplasms genetics
Testicular Neoplasms chemistry
Testicular Neoplasms mortality
Testicular Neoplasms metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1532-0979
- Volume :
- 49
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The American journal of surgical pathology
- Publication Type :
- Academic Journal
- Accession number :
- 39449577
- Full Text :
- https://doi.org/10.1097/PAS.0000000000002323