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Collision tumor of a papillary and follicular thyroid carcinoma: a case report

Authors :
Kanako Kawasaki
Keita Kai
Nariyuki Tanaka
Shinichi Kido
Arisa Ibi
Akimichi Minesaki
Moriyasu Yamauchi
Yuichiro Kuratomi
Shinichi Aishima
Masahiro Nakashima
Masahiro Ito
Source :
Thyroid Research, Vol 16, Iss 1, Pp 1-8 (2023)
Publication Year :
2023
Publisher :
BMC, 2023.

Abstract

Abstract Background Papillary thyroid carcinoma (PTC) and follicular thyroid carcinoma (FTC) are common differentiated thyroid cancers, but the detection of a collision tumor is an extremely rare event. Case presentation The patient was a 69-year-old Japanese female with multiple cervical lymph node swellings and a thyroid tumor. Preoperative fine needle aspiration cytology of the enlarged lymph node revealed a cytological diagnosis of papillary thyroid carcinoma (PTC). A total thyroidectomy, right cervical dissection and paratracheal dissection were performed. Histopathological and immunohistochemical analyses of resected specimens revealed a collision tumor of PTC and FTC. Multiple metastases of papillary carcinoma were found in the dissected lymph nodes. In the PTC lesion, IHC for BRAF (V600E) was positive but negative for the FTC lesion. Genetic analyses further revealed a TERT promoter C228T mutation in PTC and a NRAS codon 61 mutation in FTC. The patient died of recurrent cancer 8 months after surgery. Conclusions A case of a collision tumor of PTC and FTC is very rare, and even fewer cases have been subjected to genetic scrutiny. The present case was successfully diagnosed by pathological examination using immunohistochemical and genetic analyses. The TERT promoter mutation in the PTC lesion was consistent with the aggressive behavior of the cancer.

Details

Language :
English
ISSN :
17566614
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Thyroid Research
Publication Type :
Academic Journal
Accession number :
edsdoj.93e657349c243de87726fccab47f7f5
Document Type :
article
Full Text :
https://doi.org/10.1186/s13044-023-00167-3