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Published online by Cambridge University Press:  03 July 2022

Runjan Chetty
Affiliation:
University of Toronto
Kumarasen Cooper
Affiliation:
University of Pennsylvania
Carol Cheung
Affiliation:
University of Toronto
Srinivas Mandavilli
Affiliation:
Hartford Hospital
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Publisher: Cambridge University Press
Print publication year: 2022

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References

Selected references

Galietta, A, Pizzi, C, Pettinato, G, et al. Differential TAG-72 epitope expression in breast cancer and lymph node metastases: A marker of a more aggressive phenotype. Oncol Rep 2002;9:135–40.Google Scholar
Sheibani, K, Esteban, JM, Bailey, A, Battifora, H, Weiss, LM. Immunopathologic and molecular studies as an aid to the diagnosis of malignant mesothelioma. Hum Pathol 1992;23:107–16.CrossRefGoogle Scholar
Szpak, CA, Johnston, WW, Roggli, V, et al. The diagnostic distinction between malignant mesothelioma of the pleura and adenocarcinoma of the lung as defined by a monoclonal antibody B72.3. Am J Pathol 1986;122:252–60.Google Scholar

Selected references

Cork, LC, Sternberger, NH, Sternberger, LA, et al. Phosphorylated neurofilament antigens in neurofibrillary tangles in Alzheimer’s disease. J Neuropathol Exp Neurol 1986;45:5664.CrossRefGoogle ScholarPubMed
Feany, MB, Dickson, DW. Neurodegenerative disorders with extensive tau pathology: A comparative study and review. Ann Neurol 1996;40:139–48.Google Scholar
Joachim, CL, Morris, JH, Kosik, KS, Selkoe, DJ. Tau antisera recognize neurofibrillary tangles in a range of neurodegenerative disorders. Ann Neurol 1987;22:514–20.Google Scholar

Selected references

Aggarwal, M, Villuendas, R, Gomez, G, et al. TCL1A expression delineates biological and clinical variability in B-cell lymphoma. Mod Pathol 2009;22(2):206–15.Google Scholar
Cao, D, Lane, Z, Allan, RW, et al. TCL1 is a diagnostic marker for intratubular germ cell neoplasia and classic seminoma. Histopathology 2010;57(1):152–7.CrossRefGoogle ScholarPubMed
Laine, J, Kunstle, G, Obata, T, et al. The protooncogene TCL1 is an Akt kinase coactivator. Mol Cell 2000;6:395407.Google Scholar
Sangle, NA, Schmidt, RL, Patel, JL, et al. Optimized immunohistochemical panel to differentiate myeloid sarcoma from blastic plasmacytoid dendritic cell neoplasm. Mod Pathol 2014;27(8):1137–43.Google Scholar
Sun, Y, Tang, G, Hu, Z, et al. Comparison of karyotyping, TCL1 fluorescence in situ hybridisation and TCL1 immunohistochemistry in T cell prolymphocytic leukaemia. J Clin Pathol 2018;71(4):309–15.Google Scholar
Trinh, DT, Shibata, K, Hirosawa, T, et al. Diagnostic utility of CD117, CD133, SALL4, OCT4, TCL1 and glypican-3 in malignant germ cell tumors of the ovary. J Obstet Gynaecol Res 2012;38(5):841–8.CrossRefGoogle ScholarPubMed
Weissferdt, A, Rodriguez-Canales, J, Liu, H, et al. Primary mediastinal seminomas: A comprehensive immunohistochemical study with a focus on novel markers. Hum Pathol 2015;46(3):376–83.Google Scholar

Selected references

Erickson, HP, Bourdon, MA. Tenascin: An extracellular matrix protein prominent in specialized embryonic tissues and tumors. Ann Rev Cell Biol 1989;5:7192.Google Scholar
Koukoulis, GK, Gould, VE, Bhattacharyya, A, et al. Tenascin in normal, reactive, hyperplastic and neoplastic tissues: Biologic and pathologic implications. Hum Pathol 1991;22:636–43.CrossRefGoogle ScholarPubMed
Sedele, M, Karaveli, S, Pestereli, HE, et al. Tenascin expression in normal, hyperplastic and neoplastic endometrium. Int J Gynecol Pathol 2002;12:161–6.Google Scholar

Selected references

Chilosi, M, Pizzolo, G. Review of terminal deoxynucleotidyl transferase: Biological aspects, methods of detection, and selected diagnostic applications. Appl Immunohistochem 1995;3:209–21.Google Scholar
Onciu, M, Lorsbach, RB, Henry, EC, et al. Terminal deoxynucleotidyl transferase-positive lymphoid cells in reactive lymph nodes from children with malignant tumor: Incidence, distribution pattern, and immunophenotype in 26 patients. Am J Clin Pathol 2002;118:248–54.Google Scholar
Orazi, A, Cattoretti, G, Joh, K, et al. Terminal deoxynucleotidyl transferase staining of malignant lymphomas in paraffin sections. Mod Pathol 1994;7:582–6.Google Scholar

Selected references

Argani, P, Aulmann, S, Illei, PB, et al. A distinctive subset of PEComas harbors TFE3 gene fusions. Am J Surg Pathol 2010;34:1395–406.Google Scholar
Argani, P, Lal, P, Hutchinson, B, et al. Aberrant nuclear immunoreactivity for TFE3 in neoplasms with TFE3 gene fusions: A sensitive and specific immunohistochemical assay. Am J Surg Pathol 2003;27:750–61.Google Scholar

Selected references

Appleton, MAC, Attanoos, RL, Jasani, B. Thrombomodulin as a marker of vascular and lymphatic tumors. Histopathology 1996;29:153–7.Google Scholar
Attanoos, RL, Goddard, H, Gibbs, AR. Mesothelioma-binding antibodies: Thrombomodulin, OV632 and HBME-1 and their use in the diagnosis of malignant mesothelioma. Histopathology 1996;29:209–15.Google Scholar
Collins, CL, Ordonez, NG, Schaefer, R, et al. Thrombomodulin expression in malignant pleural mesothelioma and pulmonary adenocarcinoma. Am J Pathol 1992;141:827–33.Google Scholar
Ordonez, NG. Value of thrombomodulin immunostaining in the diagnosis of mesothelioma. Histopathology 1997;31:2530.Google Scholar

Selected references

De Micco, C, Ruf, J, Carayon, P, et al. Immunohistochemical study of thyroglobulin in thyroid carcinomas with monoclonal antibodies. Cancer 1987;59:471–6.Google Scholar
Wilson, NW, Pambakian, H, Richardson, TC, et al. Epithelial markers in thyroid carcinoma: An immunoperoxidase study. Histopathology 1986;10:815–29.Google Scholar

Selected references

Agoff, SN, Lamps, LW, Philip, AT, et al. Thyroid transcription factor-1 is expressed in extrapulmonary small cell carcinomas but not in other extrapulmonary neuroendocrine tumors. Mod Pathol 2000,13:238–42.Google Scholar
Bingle, CD. Thyroid transcription factor-1. Int J Biochem Cell Biol 1997;29:1471–3.CrossRefGoogle ScholarPubMed
Comperat, E, Zhang, F, Perrotin, C, et al. Variable sensitivity and specificity of TTF1 antibodies in lung metastatic adenocarcinoma of colorectal origin. Mod Pathol 2005;18: 1371–6.CrossRefGoogle ScholarPubMed

Selected references

Chen, G, Courey, AJ. Groucho/TLE family proteins and transcriptional repression. Gene 2000;249:116.Google Scholar
Duncan, VE, Wicker, JA, Kelly, DR, et al. TLE1 expression in malignant rhabdoid tumor and atypical teratoid/rhabdoid tumor. Pediatr Dev Pathol 2018;21(6):522–7.CrossRefGoogle ScholarPubMed
El Beaino, M, et al. Diagnostic value of TLE1 in synovial sarcoma: A systematic review and meta-analysis. Sarcoma 2020:7192347.CrossRefGoogle Scholar
Foo, WC, Cruise, MW, Wick, MR, et al. Immunohistochemical staining for TLE1 distinguishes synovial sarcoma from histologic mimics. Am J Clin Pathol 2011;135:839–44.Google Scholar
Jagdis, A, Rubin, BP, Tubbs, RR, et al. Prospective evaluation of TLE1 as a diagnostic immunohistochemical marker in synovial sarcoma. Am J Surg Pathol 2009;33:1743–51.CrossRefGoogle ScholarPubMed
Kosemehmetoglu, K, Vrana, JA, Folpe, AL. TLE1 expression is not specific for synovial sarcoma: A whole section study of 163 soft tissue and bone neoplasms. Mod Pathol 2009;22(7):872–8.Google Scholar
Li, WS, Liao, IC, Wen, MC, et al. BCOR-CCNB3-positive soft tissue sarcoma with round-cell and spindle-cell histology: A series of four cases highlighting the pitfall of mimicking poorly differentiated synovial sarcoma. Histopathology 2016;69(5):792801.Google Scholar
Pukhalskaya, T, Smoller, BR. TLE1 expression fails to distinguish between synovial sarcoma, atypical fibroxanthoma, and dermatofibrosarcoma protuberans. J Cutan Pathol 2020;47(2):135–8.Google Scholar
Terry, J, Saito, T, Subramanian, S, et al. TLE1 as a diagnostic immunohistochemical marker for synovial sarcoma emerging from gene expression profiling studies. Am J Surg Pathol 2007;31(2):240–6.Google Scholar
Zaccarini, DJ, Deng, X, Tull, J, et al. Expression of TLE-1 and CD99 in carcinoma: Pitfalls in diagnosis of synovial sarcoma. Appl Immunohistochem Mol Morphol 2018;26(6):368–73.CrossRefGoogle ScholarPubMed

Selected references

Di Leo, A, Larsimont, D, Gancberg, D, et al. HER-2 and topoisomerase II alpha as predictive markers in a population of node-positive breast cancer patients randomly treated with adjuvant CMF or epirubicin plus cyclophosphamide. Ann Oncol 2001;12:1081–9.Google Scholar
Gotleib, WH, Goldberg, I, Weisz, B, et al. Topoisomerase II immunostaining as a prognostic marker for survival in ovarian cancer. Gynecol Oncol 2001;82:99104.CrossRefGoogle Scholar

Selected references

Conley, FK, Jenkins, KA, Remington, JS. Toxoplasma gondii infection of the central nervous system: Use of the peroxidase-antiperoxidase method to demonstrate Toxoplasma in formalin-fixed, paraffin-embedded tissue sections. Hum Pathol 1981;12:690–8.Google Scholar
Kriek, JA, Remington, JS. Toxoplasmosis in the adult – an overview. N Engl J Med 1978;298:550–3.Google Scholar

Selected references

Hofbauer, GF, Kamarashev, J, Geertsen, R, et al. Tyrosinase immunoreactivity in formalin-fixed, paraffin-embedded primary and metastatic melanoma: Frequency and distribution. J Cutan Pathol 1998;25:204–9.Google Scholar
Jungbluth, AA, Iversen, K, Copian, K, et al. T311 – an anti-tyrosinase monoclonal antibody for the detection of melanocytic lesions in paraffin embedded tissues. Pathol Res Pract 2000;196:235–42.Google Scholar
Kaufmann, O, Koch, S, Burghardt, J, et al. Tyrosinase, Melan-A, and KBA62 as markers for the immunohistochemical identification of metastatic amelanotic melanomas on paraffin sections. Mod Pathol 1998;11:740–6.Google Scholar

Selected references

Ceccamea, A, Carlei, F, Dominici, C, et al. Correlation between tyrosine hydroxylase immunoreactive cells in tumors and urinary catecholamine output in neuroblastoma patients. Tumori 1986 31;72(5):451–7.CrossRefGoogle ScholarPubMed
Iwase, K, Nagasaka, A, Nagatsu, I, et al. Tyrosine hydroxylase indicates cell differentiation of catecholamine biosynthesis in neuroendocrine tumors. J Endocrinol Invest 1994;17:235–9.Google Scholar
Meijer, WG, Copray, SC, Hollema, H, et al. Catecholamine-synthesizing enzymes in carcinoid tumors and pheochromocytomas. Clin Chem 2003;49:586–93.Google Scholar
Takahashi, H, Wakabayashi, K, Ikuta, F, et al. Esthesioneuroblastoma: A nasal catecholamine-producing tumor of neural crest origin. Demonstration of tyrosine hydroxylase-immunoreactive tumor cells. Acta Neuropathol 1988;76:522–7.Google Scholar

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