Le Loarer F, Szuhai K, Tirode F (2020) World Health Organization (WHO) Classification of soft tissue and bone tumours, 5th ed. International Agency for Research on Cancer (IARC), Lyon: Round cell sarcoma with EWSR1-non-ETS fusions, p 326–329
Watson S, Perrin V, Guillemot D, Reynaud S, Coindre JM, Karanian M, Guinebretière JM, Freneaux P, Le Loarer F, Bouvet M, Galmiche-Rolland L, Larousserie F, Longchampt E, Ranchere-Vince D, Pierron G, Delattre O, Tirode F (2018) Transcriptomic definition of molecular subgroups of small round cell sarcomas. J Pathol 245(1):29–40. https://doi.org/10.1002/path.5053
Article CAS PubMed Google Scholar
Koelsche C, Kriegsmann M, Kommoss FKF, Stichel D, Kriegsmann K, Vokuhl C, Grünewald TGP, Romero-Pérez L, Kirchner T, de Alava E, Diaz-Martin J, Hartmann W, Baumhoer D, Antonescu CR, Szuhai K, Flucke U, Dirksen U, Pfister SM, Jones DTW, Mechtersheimer G, von Deimling A (2019) DNA methylation profiling distinguishes Ewing-like sarcoma with EWSR1-NFATc2 fusion from Ewing sarcoma. J Cancer Res Clin Oncol 145(5):1273–1281. https://doi.org/10.1007/s00432-019-02895-2
Article CAS PubMed PubMed Central Google Scholar
Wang GY, Thomas DG, Davis JL, Ng T, Patel RM, Harms PW, Betz BL, Schuetze SM, McHugh JB, Horvai AE, Cho SJ, Lucas DR (2019) EWSR1-NFATC2 Translocation-associated sarcoma clinicopathologic findings in a rare aggressive primary bone or soft tissue tumor. Am J Surg Pathol 43(8):1112–1122. https://doi.org/10.1097/PAS.0000000000001260
Perret R, Escuriol J, Velasco V, Mayeur L, Soubeyran I, Delfour C, Aubert S, Polivka M, Karanian M, Meurgey A, Le Guellec S, Weingertner N, Hoeller S, Coindre JM, Larousserie F, Pierron G, Tirode F, Le Loarer F (2020) NFATc2-rearranged sarcomas: clinicopathologic, molecular, and cytogenetic study of 7 cases with evidence of AGGRECAN as a novel diagnostic marker. Mod Pathol 33(10):1930–1944. https://doi.org/10.1038/s41379-020-0542-z
Article CAS PubMed Google Scholar
Yoshida KI, Machado I, Motoi T, Parafioriti A, Lacambra M, Ichikawa H, Kawai A, Antonescu CR, Yoshida A (2020) NKX3-1 is a useful immunohistochemical marker of EWSR1-NFATC2 sarcoma and mesenchymal chondrosarcoma. Am J Surg Pathol 44(6):719–728. https://doi.org/10.1097/PAS.0000000000001441
Article PubMed PubMed Central Google Scholar
Makise N, Yoshida KI, Iijima T, Yoshida A, Ushiku T, Ishida T (2021) Skeletal EWSR1-NFATC2 sarcoma previously diagnosed as Ewing-like adamantinoma: a case report and literature review emphasizing its unique radiological features. Pathol Int 71(9):614–620. https://doi.org/10.1111/pin.13135
Marshall AE, Cramer HM, Wu HH (2014) The usefulness of the cell transfer technique for immunocytochemistry of fine-needle aspirates. Cancer Cytopathol 122(12):898–902. https://doi.org/10.1002/cncy.21469
Wangsiricharoen S, Wakely PE Jr, Siddiqui MT, Ali SZ (2021) Cytopathology of chondromyxoid fibroma: a case series and review of the literature. J Am Soc Cytopathol 10(4):366–381. https://doi.org/10.1016/j.jasc.2021.04.001
Bommer KK, Ramzy I, Mody D (1997) Fine-needle aspiration biopsy in the diagnosis and management of bone lesions: a study of 450 cases. Cancer 81(3):148–56. https://doi.org/10.1002/(sici)1097-0142(19970625)81:3%3c148::aid-cncr4%3e3.0.co;2-n. (25)
Article CAS PubMed Google Scholar
Brcic I, Scheipl S, Bergovec M, Leithner A, Szkandera J, Sotlar K, Suda AJ, Smolle MA, Kraus T, Rosenberg AE, Liegl-Atzwanger B, Igrec J (2022) Implementation of copy number variations-based diagnostics in morphologically challenging EWSR1/FUS::NFATC2 neoplasms of the bone and soft tissue. Int J Mol Sci 23(24):16196. https://doi.org/10.3390/ijms232416196
Article PubMed PubMed Central Google Scholar
Tornóczky T, Bogner B, Krausz T, Ottóffy G, Szuhai K (2012) Angiomatoid fibrous histiocytoma: pleomorphic variant associated with multiplication of EWSR1-CREB1 fusion gene. Pathol Oncol Res 18(2):545–548. https://doi.org/10.1007/s12253-011-9468-6
Xiao S, Renshaw A, Cibas ES, Hudson TJ, Fletcher JA (1995) Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations. Am J Pathol 147(4):896–904
CAS PubMed PubMed Central Google Scholar
Lee SE, Lee EH, Park H, Sung JY, Lee HW, Kang SY, Seo S, Kim BH, Lee H, Seo AN, Ahn G, Choi YL (2012) The diagnostic utility of the GNAS mutation in patients with fibrous dysplasia: meta-analysis of 168 sporadic cases. Hum Pathol 43(8):1234–1242. https://doi.org/10.1016/j.humpath.2011.09.012
Article CAS PubMed Google Scholar
Tabareau-Delalande F, Collin C, Gomez-Brouchet A, Decouvelaere AV, Bouvier C, Larousserie F, Marie B, Delfour C, Aubert S, Rosset P, de Muret A, Pagès JC, de Pinieux G (2013) Diagnostic value of investigating GNAS mutations in fibro-osseous lesions: a retrospective study of 91 cases of fibrous dysplasia and 40 other fibro-osseous lesions. Mod Pathol 26(7):911–921. https://doi.org/10.1038/modpathol.2012.223
Comments (0)