Xiong Yiqin, Dresser Karen, Cornejo Kristine M
Pathology Resident, Department of Pathology, University of Massachusetts Medical School, UMass Memorial Medical Center, Worcester, MA.
Research Assistant, Department of Pathology, University of Massachusetts Medical School, UMass Memorial Medical Center, Worcester, MA.
Am J Dermatopathol. 2019 Jan;41(1):1-6. doi: 10.1097/DAD.0000000000001186.
TLE1 immunohistochemistry is widely used as a biomarker for synovial sarcoma. Recently, we identified TLE1 expression in a subset of melanomas and noted staining in sebaceous glands and follicular epithelium. TLE1 immunohistochemistry has not been well studied in cutaneous tumors. The aim was to investigate TLE1 expression in sebaceous neoplasms, basal cell carcinoma (BCC), and squamous cell carcinoma (SCC) to determine whether the staining patterns may aid in the diagnosis or classification of these neoplasms. TLE1 immunohistochemistry was performed on sebaceous adenoma (n = 26), sebaceoma (n = 10), sebaceous carcinoma (n = 19), BCC (n = 20), and SCC (n = 19). Positivity was defined as dark-brown nuclear staining and graded as 3+ (strong staining of >50% of cells at 4×), 2+ (moderate staining of 10-50% of cells at 4× or >50% of cells staining at 10×), and 1+ (weak staining of <50% of cells at 10×). No staining was scored as 0. A score of 2-3+ was considered positive and 0-1+ negative. Nuclear TLE1 expression was identified in 25/26 (96%) sebaceous adenomas, 8/10 (80%) sebaceomas, and 17/19 (90%) sebaceous carcinomas. TLE1 also labeled 19/20 (95%) BCCs and 12/19 (63%) SCCs. TLE1 immunohistochemistry frequently highlights sebaceous neoplasms, BCC, and SCC with a fairly high sensitivity (63%-96%). Therefore, TLE1 is not a specific biomarker for synovial sarcoma and should be evaluated with caution, particularly in cases in which the differential diagnosis may include other cutaneous tumors. In addition, TLE1 does not seem to be useful in the diagnosis or classification of these neoplasms.
TLE1免疫组化作为滑膜肉瘤的生物标志物被广泛应用。最近,我们在一部分黑色素瘤中发现了TLE1的表达,并注意到皮脂腺和毛囊上皮有染色。TLE1免疫组化在皮肤肿瘤方面尚未得到充分研究。目的是研究TLE1在皮脂腺肿瘤、基底细胞癌(BCC)和鳞状细胞癌(SCC)中的表达,以确定染色模式是否有助于这些肿瘤的诊断或分类。对皮脂腺腺瘤(n = 26)、皮脂腺瘤(n = 10)、皮脂腺癌(n = 19)、BCC(n = 20)和SCC(n = 19)进行TLE1免疫组化检测。阳性定义为深棕色核染色,并分为3+(4倍镜下>50%的细胞强染色)、2+(4倍镜下10%-50%的细胞中度染色或10倍镜下>50%的细胞染色)和1+(10倍镜下<50%的细胞弱染色)。无染色记为0。2-3+分为阳性,0-1+分为阴性。在25/26(96%)的皮脂腺腺瘤、8/10(80%)的皮脂腺瘤和17/19(90%)的皮脂腺癌中发现核TLE1表达。TLE1也标记了19/20(95%)的BCC和12/19(63%)的SCC。TLE1免疫组化经常以相当高的敏感性(63%-96%)突出皮脂腺肿瘤、BCC和SCC。因此,TLE1不是滑膜肉瘤的特异性生物标志物,应谨慎评估,尤其是在鉴别诊断可能包括其他皮肤肿瘤的病例中。此外,TLE1似乎对这些肿瘤的诊断或分类没有帮助。