Thyroid metastases: a 45-year population-based descriptive study (1979-2024).

IF 2.9
Adeline Theresette-Guilbert, Camil M'gabar, Pierre Martin, Mohamad Zalzali
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Abstract

Background: Metastases to the thyroid are rare but clinically important, as they may mimic primary thyroid malignancy and can be the first sign of recurrence of a prior solid tumor.

Methods: We conducted a retrospective descriptive population-based study using a thyroid cancer registry in northeastern France. All patients diagnosed with thyroid metastasis between 1975 and 2024 were identified; medical records and pathology reports were reviewed to confirm secondary origin and to collect demographic, clinical, pathological and treatment data. Thyroid metastases diagnosed within 6 months of the primary cancer were classified as synchronous; all others were considered metachronous. Overall survival was estimated from the dates of primary cancer diagnosis and of thyroid metastasis diagnosis using Kaplan-Meier methods and compared by primary tumor site using the log-rank test.

Results: Among the 3,647 thyroid tumors recorded between 1975 and 2024, 37 potential secondary thyroid tumors were identified; after medical record review, 8 cases were excluded (insufficient clinical data or uncertain histological origin), leaving 29 confirmed thyroid metastases. Mean age at thyroid metastasis diagnosis was 61.7 years (median 65; range 38-84), with slight male predominance (55.2%; sex ratio 1.23). Primary sites were kidney (24.1%), head and neck (20.7%), lung (17.2%) and lower gastrointestinal (13.8%). Metastases were metachronous in nearly half of the cases (48.3%). Thyroid surgery was performed in 62.1% of cases. Median survival was 5 years after initial diagnosis and 30 months after the diagnosis of thyroid metastasis. Renal cancers showed more favorable outcomes (120 vs 17 months' survival; log-rank, p=0.0037).

Conclusions: In this population-based series spanning 50 years, thyroid metastases were a rare but not exceptional clinical situation. They should be considered in the evaluation of thyroid nodules in patients with history of solid cancer. Renal primaries are associated with more favorable survival.

甲状腺转移:一项45年基于人群的描述性研究(1979-2024)。
背景:甲状腺转移是罕见的,但在临床上很重要,因为它们可能与原发性甲状腺恶性肿瘤相似,并且可能是先前实体瘤复发的第一个迹象。方法:我们在法国东北部的甲状腺癌登记处进行了一项基于人群的回顾性描述性研究。1975年至2024年间诊断为甲状腺转移的所有患者均被确诊;对医疗记录和病理报告进行了审查,以确认次要来源,并收集人口、临床、病理和治疗数据。原发癌后6个月内诊断的甲状腺转移归为同步转移;所有其他的都被认为是同步的。使用Kaplan-Meier方法从原发性肿瘤诊断日期和甲状腺转移诊断日期估计总生存期,并使用log-rank检验对原发性肿瘤部位进行比较。结果:1975 ~ 2024年记录的3647例甲状腺肿瘤中,鉴定出潜在继发性甲状腺肿瘤37例;经病历审查,排除8例(临床资料不足或组织学来源不确定),剩下29例确诊甲状腺转移。甲状腺转移诊断的平均年龄为61.7岁(中位65岁,范围38-84岁),男性略占优势(55.2%,性别比1.23)。原发部位为肾脏(24.1%)、头颈部(20.7%)、肺部(17.2%)和下胃肠道(13.8%)。近一半的病例(48.3%)发生异时性转移。62.1%的病例行甲状腺手术。中位生存期为首次诊断后5年,甲状腺转移诊断后30个月。肾癌表现出更有利的结果(120个月vs 17个月;log-rank, p=0.0037)。结论:在这个以人群为基础的跨越50年的系列研究中,甲状腺转移是一种罕见但并不例外的临床情况。在评估有实体癌病史的患者甲状腺结节时应考虑这些因素。肾脏原发与更有利的生存相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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