Prevalence and diagnostic significance of non‐invasive follicular thyroid neoplasm with papillary‐like nuclear features in Japan—A multi‐institutional study

Author:

Hirokawa Mitsuyoshi1ORCID,Ito Masahiro2ORCID,Motoi Noriko3ORCID,Chiba Tomohiro4ORCID,Imamura Yoshiaki5ORCID,Yasuoka Hironao6ORCID,Hino Rumi7ORCID,Higuchi Miyoko1ORCID,Miyauchi Akira8ORCID,Akamizu Takashi9ORCID

Affiliation:

1. Department of Diagnostic Pathology and Cytology Kuma Hospital Kobe Japan

2. Department of Pathology, National Hospital Organization (NHO) Nagasaki Medical Center Nagasaki Japan

3. Department of Pathology Saitama Cancer Center Saitama Japan

4. Division of Pathology, Cancer Institute Japanese Foundation for Cancer Research Tokyo Japan

5. Division of Diagnostic Pathology and Surgical Pathology University of Fukui Hospital Fukui Japan

6. Department of Pathology Osaka Police Hospital Osaka Japan

7. Department of Sports and Health Science Daito Bunka University Saitama Japan

8. Department of Surgery Kuma Hospital Kobe Japan

9. Department of Internal Medicine Kuma Hospital Kobe Japan

Abstract

AbstractThis multi‐institutional study investigated non‐invasive follicular thyroid neoplasm with papillary‐like nuclear features (NIFTP) frequency and its diagnostic significance in Japan. We reviewed 4008 thyroid nodules resected in six institutions before NIFTP was proposed. Overall, 26 cases diagnosed as non‐invasive encapsulated follicular variant of papillary thyroid carcinoma (PTC) and 145 cases of follicular thyroid adenoma (FTA) were included. Of these nodules, 80.8% and 31.0%, respectively, were NIFTPs. In five institutions, NIFTPs were more commonly found in FTA than in PTC nodules. When NIFTP was included with PTC, the overall prevalence was 2.3%, with rates in five institutions below 5.0% (0.8%–4.4%). One NIFTP case with nuclear score 3 revealed nodal metastasis 2.5 years post‐resection, and the carcinoma cells were immunohistochemically positive for BRAF. FTAs or NIFTPs with nuclear score 2 did not metastasize. NIFTP was more common among FTA than among PTC nodules, possibly due to underdiagnosis of PTC on nuclear findings. Considering the clinical findings, molecular pathogenesis, and therapeutic strategy in Japan, NIFTP with nuclear score 2 is not different from FTA, and use of this entity terminology is not meaningful. In contrast, NIFTP with nuclear score 3 has potential for metastasis and BRAFV600E mutation. Therefore, in NIFTP cases, nuclear scores 2 and 3 should be separately reported.

Publisher

Wiley

Subject

General Medicine,Pathology and Forensic Medicine

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