Suster David I, Bellizzi Andrew M, Mackinnon Alexander Craig, Suster Saul
Department of Pathology, Rutgers New Jersey Medical School, Newark, New Jersey, USA
Department of Pathology, University of Iowa, Carver College of Medicine, Iowa City, Iowa, USA.
J Clin Pathol. 2025 Aug 22. doi: 10.1136/jcp-2025-210045.
To investigate immunohistochemical expression of the E26 transformation-specific factors (ETS)-related gene () in a large number of soft tissue neoplasms using a tissue microarray technique.
489 cases of soft tissue neoplasms, including benign and malignant entities, were collected from the files of the respective institutions and constructed into tissue microarrays. Tissue microarrays were stained for ERG immunohistochemistry using two antibodies, EP111 and EPR3864.
A total of 25 cases (5.1%) were identified that were positive for ERG using the monoclonal antibody EP111 and 15 cases (3%) using the monoclonal antibody EPR3864, including rhabdomyosarcoma, peripheral nerve sheath tumours, synovial sarcoma, myxofibrosarcoma, epithelioid sarcoma, dermatofibrosarcoma protuberans, low-grade fibromyxoid sarcoma, nodular fasciitis and dedifferentiated liposarcoma. The most consistently stained tumours included synovial sarcoma, rhabdomyosarcoma and benign and malignant peripheral nerve sheath tumours. Various other fibroblastic proliferations, including dermatofibrosarcoma protuberans, myxofibrosarcoma, low-grade fibromyxoid sarcoma and nodular fasciitis, also showed positive staining in a small fraction of cases. One case of dedifferentiated liposarcoma showed nuclear positivity for ERG, and one case of epithelioid sarcoma was also positive.
This study supports the value of ERG as a highly sensitive and specific marker for the diagnosis of vascular neoplasms but also demonstrates rare cases of aberrant staining and underscores the need to assess soft tissue tumours using a panel of stains and interpret the results of immunohistochemistry in the appropriate histological and clinical context.
采用组织芯片技术研究E26转化特异性因子(ETS)相关基因()在大量软组织肿瘤中的免疫组化表达。
从各机构档案中收集489例软组织肿瘤病例,包括良性和恶性实体,构建组织芯片。使用两种抗体EP111和EPR3864对组织芯片进行ERG免疫组化染色。
使用单克隆抗体EP111鉴定出25例(5.1%)ERG阳性病例,使用单克隆抗体EPR3864鉴定出15例(3%)阳性病例,包括横纹肌肉瘤、周围神经鞘瘤、滑膜肉瘤、黏液纤维肉瘤、上皮样肉瘤、隆突性皮肤纤维肉瘤、低度纤维黏液样肉瘤、结节性筋膜炎和去分化脂肪肉瘤。染色最一致的肿瘤包括滑膜肉瘤、横纹肌肉瘤以及良性和恶性周围神经鞘瘤。其他各种成纤维细胞增生性病变,包括隆突性皮肤纤维肉瘤、黏液纤维肉瘤、低度纤维黏液样肉瘤和结节性筋膜炎,也有一小部分病例呈阳性染色。1例去分化脂肪肉瘤显示ERG核阳性,1例上皮样肉瘤也呈阳性。
本研究支持ERG作为诊断血管肿瘤的高度敏感和特异标志物的价值,但也显示了罕见的异常染色病例,并强调需要使用一组染色剂评估软组织肿瘤,并在适当的组织学和临床背景下解释免疫组化结果。