Tallini Giovanni, De Leo Antonio, Repaci Andrea, de Biase Dario, Bacchi Reggiani Maria Letizia, Di Nanni Doriana, Ambrosi Francesca, Di Gioia Cira, Grani Giorgio, Rhoden Kerry Jane, Solaroli Erica, Monari Fabio, Filetti Sebastiano, Durante Cosimo
Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna-Molecular Diagnostic Unit, 40138 Azienda USL di Bologna, Italy.
Pathology Unit, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, S. Orsola-Malpighi Hospital, 40138 Bologna, Italy.
Cancers (Basel). 2020 Jan 19;12(1):246. doi: 10.3390/cancers12010246.
It is unclear whether the site of origin of papillary thyroid microcarcinoma (mPTC) with respect to the thyroid surface has an influence on clinicopathologic parameters. The objectives of the study were to: (i) Accurately measure the mPTC distance from the thyroid surface; (ii) analyze whether this distance correlates with relevant clinicopathologic parameters; and (iii) investigate the impact of the site of origin of the mPTC on risk stratification. Clinicopathologic features and mutational status were analyzed and correlated with the site of origin of the mPTC in a multicenter cohort of 298 mPTCs from six Italian medical institutions. Tumors arise at a median distance of 3.5 mm below the surface of the thyroid gland. Statistical analysis identified four distinct clusters. Group A, mPTC: size ≥ 5 mm and distance of the edge of the tumor from the thyroid capsule = 0 mm; group B, mPTC: size ≥ 5 mm and distance of the edge of the tumor from the thyroid capsule > 0 mm; group C, mPTC: size < 5 mm and distance of the edge of the tumor from the thyroid capsule = 0 mm; and group D, mPTC: size < 5 mm and distance of the edge of the tumor from the thyroid capsule > 0 mm. Univariate analysis demonstrates significant differences between the groups: Group A shows the most aggressive features, and group D the most indolent ones. By multivariate analysis, group A tumors are characterized by tall cell histotype, V600E mutation, tumor fibrosis, aggressive growth with invasive features, vascular invasion, lymph node metastases, and intermediate ATA risk. The mPTC clinicopathologic features vary according to the tumor size and distance from the thyroid surface. A four-group model may be useful for risk stratification and to refine the selection of nodules to be targeted for fine needle aspiration.
甲状腺微小乳头状癌(mPTC)相对于甲状腺表面的起源部位是否会对临床病理参数产生影响尚不清楚。本研究的目的是:(i)准确测量mPTC距甲状腺表面的距离;(ii)分析该距离是否与相关临床病理参数相关;(iii)研究mPTC的起源部位对风险分层的影响。在一个来自意大利六个医疗机构的298例mPTC多中心队列中,分析了临床病理特征和突变状态,并将其与mPTC的起源部位相关联。肿瘤起源于甲状腺表面以下3.5mm的中位距离处。统计分析确定了四个不同的组。A组,mPTC:大小≥5mm且肿瘤边缘距甲状腺被膜的距离 = 0mm;B组,mPTC:大小≥5mm且肿瘤边缘距甲状腺被膜的距离>0mm;C组,mPTC:大小<5mm且肿瘤边缘距甲状腺被膜的距离 = 0mm;D组,mPTC:大小<5mm且肿瘤边缘距甲状腺被膜的距离>0mm。单因素分析显示各组之间存在显著差异:A组表现出最具侵袭性的特征,而D组表现出最惰性的特征。多因素分析显示,A组肿瘤的特征为高细胞组织学类型、V600E突变、肿瘤纤维化、具有侵袭特征的侵袭性生长、血管侵犯、淋巴结转移和ATA风险分层为中级。mPTC的临床病理特征因肿瘤大小和距甲状腺表面的距离而异。一个四组模型可能有助于风险分层,并优化细针穿刺活检结节的选择。