Two unusual epithelial c ell phenotypes allow to detect papillary carcinoma in fine-needle aspirates of the thyroid
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Keywords

diagnostic cytology, fine-needle aspiration, papillary thyroid carcinoma

How to Cite

Bozhok, Y., & Nikonenko , A. (2024). Two unusual epithelial c ell phenotypes allow to detect papillary carcinoma in fine-needle aspirates of the thyroid. Endokrynologia, 29(2), 126-134. https://doi.org/10.31793/1680-1466.2024.29-2.126

Abstract

Fine needle aspiration (FNA) biopsy is the most commonly used method for diagnosing papillary thyroid carcinoma (PTC) and other thyroid lesions. However, cytomorphologic markers of PTC currently used in diagnostic FNA cytology are insufficiently specific. They are observed in both malignant and benign lesions, expressed by cells of not every PTC subtype and by a varying fraction of the tumor cell population. The aim was to examine new morphological markers of PTC applicable in FNA smears of a thyroid gland material. Material and methods. The study material included FNA smears of nodular goiter (n=620), follicular
thyroid adenoma (n=332), Hashimoto’s thyroiditis (n=54), oncocytic cell lesions (n=50), follicular thyroid carcinoma (n=22), medullary thyroid carcinoma (n=42), and PTC (n=280). FNA smears from patients of both sexes (1164 women and 236 men) aged from 17 to 87 years were examined. To analyze them cytochemistry, immunocytochemistry and computer morphometry were applied. Results. Two unusual epithelial cell phenotypes were identified in FNA smears of PTC but never in smears of benign and non-PTC malignant lesions of the thyroid. Cytokeratin (CK) immunocytochemistry indicated the epithelial origin of these enlarged and pleomorphic cells. Key features of the first cell phenotype included a clear cytoplasm, sharply-delineated cell borders strongly refracting light, low or negative reaction for thyroglobulin, and epCAM-negativity. Cells of the second phenotype possessed a RNA-containing macula, displayed thyroglobulin-positivity and specific pattern of epCAM expression. The question whether cells of the two identified phenotypes are related cell forms is open to discussion. Conclusions. The cells revealed are observed only in PTC and, thus, can be used as highly specific morphological markers having a potential to improve the reliability of PTC detection in Giemsa-stained conventional FNA smears of the thyroid. The unusual morphology of these cells permits their easy identification without time-consuming immunocytochemistry.

https://doi.org/10.31793/1680-1466.2024.29-2.126
pdf (Українська)

References

Sherman SI. Thyroid carcinoma. Lancet. 2003 Feb 8;361(9356):501-11. doi: 10.1016/s0140-6736(03)12488-9.

Galera-Davidson H, Gonzalez-Campora R. Thyroid. In: Bibbo M, Wilbur DC. (eds.) Comprehensive Cytopathology, Philadelphia, USA: Saunders/Elsevier; 2008. p.633-70.

Bozhok Y, Greenebaum E, Bogdanova TI, McConnell RJ, Zelinskaya A, Brenner AV, et al. NA cohort study of thyroid cancer and other thyroid diseases after the Chernobyl accident: cytohistopathologic correlation and accuracy of fine-needle aspiration biopsy in nodules detected during the first screening in Ukraine (1998-2000). Cancer. 2009 Apr 25;117(2):73-81. doi: 10.1002/cncy.20002.

Clark DP, Faquin WC. Thyroid cytopathology (Essentials in cytopathology). New York: Springer; 2010.

Bozhok YM, Golovko O, Nikonenko AG. nPAsym: an open-source plugin for ImageJ to quantify nuclear shape asymmetry. Comput Methods Programs Biomed. 2020 Nov;196:105562. doi: 10.1016/j.cmpb.2020.105562.

Cong B, Cagan RL. Cell competition and cancer from Drosophila to mammals. Oncogenesis. 2024 Jan 3;13(1):1. doi: 10.1038/s41389-023-00505-y.

Fennell KA, Vassiliadis D, Lam EYN, Martelotto LG, Balic JJ, Hollizeck S, et al. Non-genetic determinants of malignant clonal fitness at single-cell resolution. Nature. 2022 Jan;601(7891):125-31. doi: 10.1038/s41586-021-04206-7.

Lloyd RV, Osamura RY, Kloppel G, Rosai J. (eds.) WHO classification of tumours of endocrine organs: 4th ed. Lyon: IARC Press; 2017.

Nikonenko AG, Bozhok YM. Patterns of papillary thyroid carcinoma cells analyzed in fine-needle aspiration smears may reveal changes in tumor cell behavior. Diagn Cytopathol. 2012 May;40 Suppl 1:E55-61. doi: 10.1002/dc.21695.

Rosignolo F, Maggisano V, Sponziello M, Celano M, Di Gioia CR, D’Agostino M, et al. Reduced expression of THRβ in papillary thyroid carcinomas: relationship with BRAF mutation, aggressiveness and miR expression. J Endocrinol Invest. 2015 Dec;38(12):1283-9. doi: 10.1007/s40618-015-0309-4.

DeLellis RA, Shin SJ, Treaba DO. Immunohistology of endocrine tumors. In: Dabbs DJ. (ed.) Diagnostic Immunohistochemistry. Philadelphia: Saunders/Elsevier; 2010. p.291-339.

Yang GC, Fried K, Scognamiglio T. Cytological features of clear cell thyroid tumors, including a papillary thyroid carcinoma with prominent hobnail features. Diagn Cytopathol. 2013 Sep;41(9):757-61. doi: 10.1002/dc.22935.

Morrison C, Wakely P Jr. Aspiration cytopathology of metastatic mucinous papillary thyroid carcinoma. Mod Pathol. 2001 Apr;14(4):361-5. doi: 10.1038/modpathol.3880316.

Harshan M, Crapanzano JP, Aslan DL, Vazquez MF, Saqi A. Papillary thyroid carcinoma with atypical histiocytoid cells on fine-needle aspiration. Diagn Cytopathol. 2009 Apr;37(4):244-50. doi: 10.1002/dc.20990.

Bozhok YuM, Nikonenko AG. A strategy to search for new cytologic criteria in the differential diagnostics of thyroid cancers based on current (post-Chernobyl) practice in Ukraine. In: Kakudo K. (ed.) Thyroid FNA cytology. Differential diagnoses and pitfalls, Singapore: Springer Nature; 2019. p.565-77.

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