Molecular profile of follicular tumors of the thyroid gland

D. Dolidze, A. Shabunin, S. D. Сovantsev, Z. A. Bagateliya, Y. Kobzev, D. L. Rotin, K. Mulaeva, M. V. Kovaleva
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Abstract

More than 90 % of newly diagnosed cases of endocrine cancer occur in the thyroid gland. Introduction of fine needle puncture of the thyroid gland, with the classification of cytological material according to the Bethesda system, has become the cornerstone of the diagnosis of malignant neoplasms of the thyroid gland. However, traditionally in this classification there remains a weak link called a follicular tumor (category IV). The detection of a follicular tumor in the cytological material does not allow one to reliably classify the mass as benign or malignant and requires surgical intervention with morphological verification. In recent years, the possibilities of molecular genetic testing have improved markedly. Follicular tumors tend to accumulate mutations, which over time can lead to malignant transformation, but can also be used as a method of timely diagnosis. This review analyzes the literature on the possibilities of molecular genetic testing in assessing the malignant potential of follicular formations of the thyroid gland.
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甲状腺滤泡性肿瘤的分子特征
超过90%的新诊断的内分泌癌病例发生在甲状腺。采用细针穿刺甲状腺,根据Bethesda系统对细胞学物质进行分类,已成为甲状腺恶性肿瘤诊断的基石。然而,在传统的分类中,仍然存在一个称为滤泡性肿瘤(IV类)的薄弱环节。在细胞学材料中检测滤泡性肿瘤不能可靠地将肿块分类为良性或恶性,需要手术干预并进行形态学验证。近年来,分子基因检测的可能性显著提高。滤泡性肿瘤往往会积累突变,随着时间的推移可能导致恶性转化,但也可以作为及时诊断的一种方法。这篇综述分析了分子基因检测在评估甲状腺滤泡形成恶性潜能方面的可能性的文献。
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