Brčić Iva, Godschachner Theresa Marie, Igrec Jasminka, Scheipl Susanne, Smolle Anna Maria, Leithner Andreas, Szkandera Joanna, Liegl-Atzwanger Bernadette
Diagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Division of General Radiology, Department of Radiology, Medical University of Graz, Graz, Austria.
Pathology. 2025 Aug;57(5):579-584. doi: 10.1016/j.pathol.2024.11.013. Epub 2025 Feb 12.
Chromosomal rearrangement can be identified by direct methods or by using immunohistochemistry for a component of the fusion oncoprotein as a surrogate marker. Our aim was to gain insights into the staining profile using novel SS18-SSX and SSX c-terminus antibodies in SS18 fusion tumours and to investigate their potential use in soft tissue tumours harbouring SSX fusion partner outside the spectrum of synovial sarcoma. A retrospective analysis of 310 soft tissue sarcomas [via tissue microarray (TMA)] diagnosed at our Institution between 1999 and 2019 was performed. As controls, whole tissue sections from 14 genetically confirmed synovial sarcomas and one EWSR1::SSX2 rearranged sarcoma diagnosed between 2020 and 2023 were included. Two different antibodies for SSX locus were used: SSX c-terminus and SS18-SSX. Twenty-one of 310 (6.8%) and 25 of 310 (8.1%) sarcomas on the TMA showed nuclear staining with SS18-SSX and SSX, respectively. From the 24 synovial sarcomas, 17 (70.8%) stained positive for both antibodies, and in five of these cases, nuclear staining for SSX was weak. In four (16.7%) cases, only SS18-SSX was positive, and in three (12.5%) cases, only SSX staining was found. Furthermore, SSX nuclear expression was only found in four of 62 (6.5%) myxofibrosarcomas. In the control cohort, 11 of 14 synovial sarcomas (78.6%) showed positive staining for both antibodies. The remaining three cases were negative for SS18-SSX, but demonstrated at least focally strong positivity for SSX. The EWSR1::SSX2 rearranged sarcoma showed strong nuclear positivity for SSX. SS18-SSX and SSX c-terminus antibodies are reliable diagnostic markers that can be used as a surrogate marker for identification of a specific fusion. The SS18-SSX antibody is more specific and shows strong nuclear staining in synovial sarcomas, whereas SSX can present with weak staining and is less specific. However, the latter can be used in soft tissue tumours harbouring SSX fusion partner outside the spectrum of synovial sarcoma.
染色体重排可通过直接方法或使用免疫组织化学检测融合癌蛋白的一个组成部分作为替代标志物来识别。我们的目的是利用新型的SS18 - SSX和SSX C末端抗体深入了解SS18融合肿瘤的染色情况,并研究它们在滑膜肉瘤谱系之外携带SSX融合伴侣的软组织肿瘤中的潜在用途。对1999年至2019年在我们机构诊断的310例软组织肉瘤(通过组织微阵列(TMA))进行了回顾性分析。作为对照,纳入了2020年至2023年期间诊断的14例基因确诊的滑膜肉瘤和1例EWSR1::SSX2重排肉瘤的全组织切片。使用了两种针对SSX基因座的不同抗体:SSX C末端和SS18 - SSX。TMA上310例肉瘤中有21例(6.8%)和25例(8.1%)分别显示SS18 - SSX和SSX的核染色。在24例滑膜肉瘤中,17例(70.8%)两种抗体均呈阳性染色,其中5例SSX的核染色较弱。4例(16.7%)仅SS18 - SSX呈阳性,3例(12.5%)仅发现SSX染色。此外,在62例黏液纤维肉瘤中仅4例(6.5%)发现SSX核表达。在对照队列中,14例滑膜肉瘤中有11例(78.6%)两种抗体均呈阳性染色。其余3例SS18 - SSX呈阴性,但SSX至少局灶性呈强阳性。EWSR1::SSX2重排肉瘤显示SSX核强阳性。SS18 - SSX和SSX C末端抗体是可靠的诊断标志物,可作为识别特定融合的替代标志物。SS18 - SSX抗体更具特异性,在滑膜肉瘤中显示强核染色,而SSX可能染色较弱且特异性较低。然而,后者可用于滑膜肉瘤谱系之外携带SSX融合伴侣的软组织肿瘤。