Kawasaki Kanako, Kai Keita, Tanaka Nariyuki, Kido Shinichi, Ibi Arisa, Minesaki Akimichi, Yamauchi Moriyasu, Kuratomi Yuichiro, Aishima Shinichi, Nakashima Masahiro, Ito Masahiro
Department of Pathology & Microbiology, Saga University Faculty of Medicine, Saga, Japan.
Department of Otolaryngology - Head & Neck Surgery, Saga University Faculty of Medicine, Saga, Japan.
Thyroid Res. 2023 Aug 7;16(1):24. doi: 10.1186/s13044-023-00167-3.
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.
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.
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.
甲状腺乳头状癌(PTC)和甲状腺滤泡状癌(FTC)是常见的分化型甲状腺癌,但同时发生碰撞瘤的情况极为罕见。
患者为一名69岁的日本女性,有多处颈部淋巴结肿大及甲状腺肿瘤。对肿大淋巴结进行术前细针穿刺细胞学检查,结果显示为甲状腺乳头状癌(PTC)的细胞学诊断。遂行全甲状腺切除术、右侧颈部清扫术及气管旁清扫术。对切除标本进行组织病理学和免疫组化分析,发现为PTC与FTC的碰撞瘤。在清扫的淋巴结中发现了乳头状癌的多处转移。在PTC病灶中,BRAF(V600E)免疫组化呈阳性,而在FTC病灶中呈阴性。基因分析进一步显示,PTC存在TERT启动子C228T突变,FTC存在NRAS密码子61突变。患者术后8个月死于癌症复发。
PTC与FTC碰撞瘤的病例非常罕见,接受基因检查的病例更少。本病例通过免疫组化和基因分析的病理检查得以成功诊断。PTC病灶中的TERT启动子突变与癌症的侵袭性行为一致。