Wu L, Jiao Q, Tang J, Jin J Z, Su X L, Liu Z Y
Department of Pathology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200233, China.
Zhonghua Bing Li Xue Za Zhi. 2025 May 8;54(5):518-523. doi: 10.3760/cma.j.cn112151-20241125-00783.
To investigate the cytopathological features of thyroid tumor with DICER1 mutation. A retrospective study on the preoperative cell smear was conducted on thyroid tumors with DICER1 gene mutations detected by Sanger sequencing in the Department of Pathology Shanghai Sixth People's Hospital affiliated to Shanghai Jiaotong University School of Medicine from May 2022 to November 2024. Totally 163 cases with histological features indicating DICER1 mutation related thyroid tumor underwent Sanger sequencing. Fifteen cases were confirmed to harbor DICER1 mutation (15/163,9.2%). Fourteen of 15 patients were female, and only 1 was male; average age 42(31,47) years. Eight cases presented with D1709 hotspot mutation (8/15) and 7 cases with the E1813 hotspot mutation (7/15) and there was no statistical significant difference between mutation rate of different hotspot (=0.620,=0.438). All specimens were stained with hematoxylin-eosin staining. A moderate number of cells were observed for all cases, predominantly with macrofollicular pattern and rare small papillae. The cell nuclei were mainly uniform, small, round and dark, slightly enlarged or medium-sized. Several cases could also present RAS-like nuclear features: 3 cases showed visible nuclear grooves. According to the expert consensus on the cytopathological diagnosis of thyroid fine needle aspiration (version 2023),the cytopathological diagnostic categories were: Ⅱ, 6 cases; Ⅲ, 2 cases; Ⅳ, 6 cases; and Ⅴ, 1 case. Postoperative histological diagnoses included follicular thyroid carcinoma in 2 cases, high-grade differentiated thyroid carcinoma in 1 case, follicular thyroid adenoma in 3 cases, follicular thyroid tumor of undetermined malignant potential in 4 case, and thyroid follicular nodular disease in 5 cases. The morphological features of DICER1-mutated thyroid tumors are predominant macrofollicles, with uniformly small round and dark nuclei. It is difficult to identify typically diagnostic atrophic follicles on cell smear, leading to a preoperative diagnosis of benign non-neoplastic or indeterminate category. Therefore, it is necessary to carefully observe the macro-follicles and small round dark nuclear features, which is necessary to suggest a genetic test of DICER1 gene and to confirm the diagnosis before surgery.
探讨DICER1突变型甲状腺肿瘤的细胞病理学特征。对上海交通大学医学院附属第六人民医院病理科2022年5月至2024年11月期间经Sanger测序检测出DICER1基因突变的甲状腺肿瘤患者的术前细胞涂片进行回顾性研究。共有163例具有提示DICER1突变相关甲状腺肿瘤组织学特征的病例接受了Sanger测序。15例被证实存在DICER1突变(15/163,9.2%)。15例患者中14例为女性,仅1例为男性;平均年龄42(31,47)岁。8例出现D1709热点突变(8/15),7例出现E1813热点突变(七/十五),不同热点突变率之间无统计学差异(=0.620,=0.438)。所有标本均进行苏木精-伊红染色。所有病例均观察到中等数量的细胞,主要为大滤泡型,罕见小乳头。细胞核主要均匀、小、圆形且深染,略有增大或中等大小。部分病例还可呈现RAS样核特征:3例可见核沟。根据甲状腺细针穿刺细胞病理学诊断专家共识(2023版),细胞病理学诊断分类为:Ⅱ类6例;Ⅲ类2例;Ⅳ类6例;Ⅴ类1例。术后组织学诊断包括滤泡状甲状腺癌2例,高分化甲状腺癌1例,滤泡状甲状腺腺瘤3例,具有不确定恶性潜能的滤泡状甲状腺肿瘤4例,甲状腺滤泡结节病5例。DICER1突变型甲状腺肿瘤的形态学特征以大滤泡为主,细胞核均匀、小、圆形且深染。在细胞涂片上难以识别典型的诊断性萎缩滤泡,导致术前诊断为良性非肿瘤性或不确定类别。因此,有必要仔细观察大滤泡和小圆形深染核特征,建议进行DICER1基因检测并在手术前确诊。