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A Multi-institutional Study of Prevalence and Clinicopathologic Features of Non-invasive Follicular Thyroid Neoplasm with Papillary-like Nuclear Features (NIFTP) in Korea

Authors
Seo, Ja YeongPark, Ji HyunPyo, Ju YeonCha, Yoon JinJung, Chan KwonSong, Dong EunKwak, Jeong JaPark, So YeonNa, Hee YoungKim, Jang-HeeSeok, Jae YeonKim, Hee SungHong, Soon Won
Issue Date
Nov-2019
Publisher
KOREAN SOC PATHOLOGISTS
Keywords
Thyroid carcinoma; Follicular variant; Papillary carcinoma; Non-invasive follicular thyroid neoplasm with papillary-like nuclear features
Citation
JOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE, v.53, no.6, pp.378 - 385
Journal Title
JOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE
Volume
53
Number
6
Start Page
378
End Page
385
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/17989
DOI
10.4132/jptm.2019.09.18
ISSN
2383-7837
Abstract
Background: In the present multi-institutional study, the prevalence and clinicopathologic characteristics of non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) were evaluated among Korean patients who underwent thyroidectomy for papillary thyroid carcinoma (PTC). Methods: Data from 18,819 patients with PTC from eight university hospitals between January 2012 and February 2018 were retrospectively evaluated. Pathology reports of all PTCs and slides of potential NIFTP cases were reviewed. The strict criterion of no papillae was applied for the diagnosis of METE Due to assumptions regarding misclassification of NIFTP as non-PTC tumors, the lower boundary of NIFTP prevalence among PTCs was estimated. Mutational analysis for BRAF and three RAS isoforms was performed in 27 randomly selected NIFTP cases. Results: The prevalence of NIFTP was 1.3% (238/18,819) of all PTCs when the same histologic criteria were applied for NIFTP regardless of the tumor size but decreased to 0.8% (152/18,819) when tumors >= 1 cm in size were included. The mean follow-up was 37.7 months and no patient with NIFTP had evidence of lymph node metastasis, distant metastasis, or disease recurrence during the follow-up period. A difference in prevalence of NIFTP before and after NIFTP introduction was not observed. BRAP(V600E) mutation was not found in NIFTP. The mutation rate for the three RAS genes was 55.6% (15/27). Conclusions: The low prevalence and indolent clinical outcome of NIFTP in Korea was confirmed using the largest number of cases to date. The introduction of NIFTP may have a small overall impact in Korean practice.
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