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术前检测到启动子突变但无[具体缺失内容未给出]的甲状腺结节的病理诊断:一项包含52例病例的双中心研究系列

Pathological Diagnosis of Thyroid Nodules with Preoperatively Detected Promoter Mutations in the Absence of : A Bi-Center Series of 52 Cases.

作者信息

Alzumaili Bayan A, Instrum Ryan, Alabkaa Anas, Sadow Peter M, Tuttle Michael R, Xu Bin, Morris Luc G T, Ghossein Ronald A

机构信息

Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

出版信息

Thyroid. 2025 Jul 28. doi: 10.1177/10507256251363450.

Abstract

Mutations in the promoter region of () in thyroid nodules with indeterminate cytology are quoted to confer a high (∼80-95%) probability for thyroid carcinoma when detected on genomic classifier (GC) ThyroSeq. mutations may also occur in benign and low-risk thyroid neoplasms, and the risk of malignancy (ROM) in nodules harboring mutations without is unknown. We analyzed the ROM and the surgical diagnosis in a retrospective cohort of thyroid nodules with treated at two academic medical centers. From 2323 patients with ThyroSeq GC performed on preoperative fine needle aspiration samples, 52 cases (2.3%) were identified harboring mutations without coexisting . The surgical diagnosis was obtained from resection ( = 51) or biopsy ( = 1, anaplastic thyroid carcinoma). The ROM was 65%. The reviewed diagnoses were benign/low-risk neoplasms in 18 (35%), carcinoma-American Thyroid Association (ATA) low/intermediate-risk in 14 (27%), and carcinoma-ATA high-risk in 20 (38.5%). All 18 benign or low-risk neoplasms had their tumor capsule submitted entirely, and 78% underwent total thyroidectomy. The molecular alterations were substratified into four groups: alone ( = 21, 40%), + ( = 18, 35%), + other non- mutation ( = 8, 15%), and + + other alterations ( = 5, 10%), and the ROM for each group was 57%, 78%, 50%, and 80%, respectively. The frequency of a high-risk malignancy, which would often lead to a recommendation for total thyroidectomy, was 9.5%, 44.5%, 37.5%, and 80%, respectively. The frequency of high-risk carcinomas was significantly higher when a nodule harbored and other concomitant alterations (48%) compared with alone (9.5%; = 0.006). Thirty five percent of nodules without are benign/low-risk thyroid neoplasms, leading to their overtreatment. The incidence of high-risk carcinomas increases in -mutated nodules with the presence of additional mutations. If the indolent histology found in these lesions is confirmed at the behavior level, lobectomy may be sufficient for the initial management of thyroid nodules without as long as there is no aggressive clinical or imaging feature. This will spare many patients from the side effects of total thyroidectomy.

摘要

在甲状腺细针穿刺活检结果不确定的甲状腺结节中,()启动子区域的突变在通过基因组分类器(GC)ThyroSeq检测到时,被认为有很高(约80 - 95%)的概率发展为甲状腺癌。 突变也可能发生在良性和低风险甲状腺肿瘤中,而在仅存在 突变而无 的结节中,其恶性风险(ROM)尚不清楚。我们分析了在两个学术医学中心接受治疗的一组甲状腺结节患者的ROM及手术诊断情况。在2323例对术前细针穿刺样本进行ThyroSeq GC检测的患者中,52例(2.3%)被确定仅存在 突变而无并存 。手术诊断通过切除(n = 51)或活检(n = 1,未分化甲状腺癌)获得。ROM为65%。复查诊断结果为良性/低风险肿瘤18例(35%)、美国甲状腺协会(ATA)低/中风险癌14例(27%)、ATA高风险癌20例(38.5%)。所有18例良性或低风险肿瘤均完整提交了肿瘤包膜,78%接受了甲状腺全切术。分子改变被分为四组:单独 (n = 21,40%)、 + (n = 18,35%)、 + 其他非 突变(n = 8,15%)、 + + 其他改变(n = 5,10%),每组的ROM分别为57%、78%、50%和80%。通常会导致建议进行甲状腺全切术的高风险恶性肿瘤的发生率分别为9.5%、44.5%、37.5%和80%。当结节同时存在 及其他伴随改变时,高风险癌的发生率显著高于单独存在 时(48%对比9.5%;P = 0.006)。35%仅存在 突变的甲状腺结节为良性/低风险甲状腺肿瘤,导致过度治疗。在存在额外突变的 突变结节中,高风险癌的发生率增加。如果这些病变中发现的惰性组织学特征在行为层面得到证实,对于无 的 甲状腺结节,只要没有侵袭性的临床或影像学特征,叶切除术可能足以作为初始治疗方法。这将使许多患者免受甲状腺全切术的副作用影响。

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