Department of Pathology, Centro Hospitalar S. João, Porto, Portugal.
Department of Pathology, Medical Faculty of the University of Porto, Porto, Portugal.
Endocr Relat Cancer. 2018 Apr;25(4):R247-R258. doi: 10.1530/ERC-17-0513. Epub 2018 Feb 9.
The 2017 edition of the WHO book on Classification of Tumours of Endocrine Organs includes a new section entitled 'Other encapsulated follicular-patterned thyroid tumours', in which the newly created NIFTP (non-invasive follicular thyroid neoplasm with papillary-like nuclear features) is identified and described in detail. Despite deleting the word 'carcinoma' from its name, NIFTP is not a benign tumor either and is best regarded as a neoplasm with 'very low malignant potential'. The main goal of the introduction of NIFTP category is to prevent overdiagnosis and overtreatment. Sampling constraints, especially when dealing with heterogeneous and/or large nodules, and difficulties in the invasiveness evaluation, are the major weaknesses of the histological characterization of NIFTP. At the cytological level, NIFTP can be separated from classic papillary carcinoma (cPTC) but not from encapsulated, invasive follicular variant PTC. The impact of NIFTP individualization for cytopathology is the drop of rates of malignancy for each Bethesda category in general and for indeterminate categories in particular. The biggest impact will be seen in institutions with a high frequency of FVPTC. The introduction of NIFTP has changed the utility of predictive values of molecular tests because mutations and rearrangements are frequently detected in NIFTP. This turns less promising the application of mutation detection panels as indicators of malignancy and will probably contribute to switch to a rule-out approach of molecular testing. Selection for surgery will go on being determined by a combined detection of clinical, cytological and ultrasound suspicious features.
世界卫生组织(WHO)2017 年版《内分泌器官肿瘤分类》新增了“其他包膜滤泡型甲状腺肿瘤”一节,其中详细介绍和定义了新创建的非浸润性滤泡性甲状腺肿瘤伴乳头状核特征(NIFTP)。尽管 NIFTP 名称中删除了“癌”一词,但它也不是良性肿瘤,最好被视为“恶性潜能非常低”的肿瘤。引入 NIFTP 类别的主要目的是防止过度诊断和过度治疗。采样限制,特别是在处理异质性和/或大结节以及侵袭性评估困难时,是 NIFTP 组织学特征的主要弱点。在细胞学水平上,NIFTP 可以与经典的甲状腺乳头状癌(cPTC)区分开来,但不能与包膜内浸润性滤泡变异型 PTC 区分开来。NIFTP 个体化对细胞病理学的影响是各 Bethesda 类别恶性率的普遍下降,尤其是不确定类别。影响最大的将是在滤泡状为主型 PTC 发生率高的机构。NIFTP 的引入改变了分子检测预测值的应用,因为 NIFTP 中经常检测到 突变和 重排。这使得突变检测面板作为恶性指标的应用不太有前景,可能会促使向分子检测排除方法转变。手术选择将继续由临床、细胞学和超声可疑特征的综合检测决定。