Andrade de Almeida M, Canão P, Capela J, Sá Couto P, Carneiro S
Faculty of Medicine, University of Porto, Porto, Portugal.
General Surgery Department, São João Local Health Unit, Porto, Portugal.
Langenbecks Arch Surg. 2025 Jul 1;410(1):204. doi: 10.1007/s00423-025-03788-4.
Non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) is a premalignant tumor formerly known as non-invasive encapsulated follicular variant of papillary thyroid carcinoma. The aim of this study was to investigate the clinicopathological traits of NIFTP to discern them from well-differentiated cancers and potentially avoid overtreatment.
We conducted a retrospective cohort study of NIFTP cases from July 2017 to November 2022 at our center. A review of demographic, clinical, sonographic, cytologic and surgical data was performed.
During the study period 70 NIFTP cases were included. Among the cohort 74.3% (52/70) were women and the mean age was 55 years (range, 25–84). The majority of patients presented euthyroid (92.9%). Median NIFTP size was 2.5 cm (range, 1.0-10.8). Most nodules displayed low or intermediate risk on ultrasound being labeled EU-TIRADS 3 (46/70, 65.7%) and EU-TIRADS 4 (23/70, 32.9%). In cytology they were typically diagnosed as Bethesda III (15/70, 21.4%) or Bethesda IV (41/70, 58.6%). Regarding surgical procedures, 36 patients (51.4%) underwent lobo-isthmectomy and 34 patients (48.6%) received total thyroidectomy. Thirteen patients (18.6%) had coexisting microcarcinomas. No patients received radioiodine ablation. After a median follow-up of 27.5 months, no structural or biochemical recurrences were observed.
Non-suspect thyroid nodules on preoperative ultrasound when combined with an indeterminate cytology and altered molecular profile should raise awareness towards the possibility of NIFTP. Even though neither FNAB nor CNB are definitive for NIFTP, CNB may be considered when additional architectural assessment is needed. Management with lobectomy seems to suffice unless total thyroidectomy is justified.
具有乳头状核特征的非侵袭性滤泡性甲状腺肿瘤(NIFTP)是一种癌前肿瘤,以前称为非侵袭性包裹性滤泡性乳头状甲状腺癌。本研究的目的是调查NIFTP的临床病理特征,以将其与高分化癌区分开来,并可能避免过度治疗。
我们对2017年7月至2022年11月在本中心的NIFTP病例进行了一项回顾性队列研究。对人口统计学、临床、超声、细胞学和手术数据进行了回顾。
在研究期间,纳入了70例NIFTP病例。在该队列中,74.3%(52/70)为女性,平均年龄为55岁(范围25-84岁)。大多数患者甲状腺功能正常(92.9%)。NIFTP的中位大小为2.5cm(范围1.0-10.8)。大多数结节在超声上显示低风险或中风险,被标记为EU-TIRADS 3(46/70,65.7%)和EU-TIRADS 4(23/70,32.9%)。在细胞学上,它们通常被诊断为贝塞斯达III级(15/70,21.4%)或贝塞斯达IV级(41/70,58.6%)。关于手术方式,36例患者(51.4%)接受了甲状腺叶峡部切除术,34例患者(48.6%)接受了全甲状腺切除术。13例患者(18.6%)合并微小癌。没有患者接受放射性碘消融。中位随访27.5个月后,未观察到结构或生化复发。
术前超声检查中无可疑的甲状腺结节,结合不确定的细胞学检查和改变的分子特征,应提高对NIFTP可能性的认识。尽管细针穿刺活检(FNAB)和粗针穿刺活检(CNB)对NIFTP都不是确诊性的,但在需要额外的结构评估时,可以考虑CNB。除非有充分理由进行全甲状腺切除术,否则甲状腺叶切除术似乎就足够了。