TERT Promoter Mutation in an Aggressive Cribriform Morular Variant of Papillary Thyroid Carcinoma

被引:0
作者
Eun Ji Oh
Sohee Lee
Ja Seong Bae
Yourha Kim
Sora Jeon
Chan Kwon Jung
机构
[1] The Catholic University of Korea,Department of Hospital Pathology, Seoul St. Mary’s Hospital, College of Medicine
[2] The Catholic University of Korea,Department of Surgery, Seoul St. Mary’s Hosptial, College of Medicine
[3] The Catholic University of Korea,Department of Biomedicine & Health Sciences
来源
Endocrine Pathology | 2017年 / 28卷
关键词
Papillary thyroid carcinoma; Cribriform-morular variant; Telomerase reverse transcriptase; Biomarker;
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学科分类号
摘要
The cribriform-morular variant of papillary thyroid carcinoma (CMV-PTC) is a rare thyroid neoplasm characterized by unique morphologic findings and association with familial adenomatous polyposis. The biologic behavior of this variant has been reported to behave similarly to classic PTC. We report a rare sporadic case of CMV-PTC occurring in a 45-year-old female with multiple lymph nodes and bone metastases, which were detected after total thyroidectomy and radioactive iodine remnant ablation. Molecular analyses of primary thyroid and metastatic tumor tissues revealed a telomerase reverse transcriptase (TERT) promoter mutation, but absence of BRAF, KRAS, NRAS, HRAS, and PIK3CA mutations. Over a 4-year follow-up period, structurally identifiable bone metastases were persistent, but serial post-operative serum thyroglobulin levels remained undetectable in the absence of thyroglobulin antibody. The literature was reviewed. This is the first case of aggressive CMV-PTC showing TERT promoter mutation. TERT promoter mutations may help in predicting aggressive clinical behavior in CMV-PTC. Postoperative serum thyroglobulin measurement may have no impact on clinical decision-making in this type of tumor.
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页码:49 / 53
页数:4
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  • [1] Harach HR(1994)Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm Histopathology 25 549-561
  • [2] Williams GT(2004)Cribriform-morular variant of papillary thyroid carcinoma: clue to early detection of familial adenomatous polyposis-associated colon cancer World J Surg 28 886-889
  • [3] Williams ED(2009)The cytological, clinical, and pathological features of the cribriform-morular variant of papillary thyroid carcinoma and mutation analysis of CTNNB1 and BRAF genes Thyroid 19 905-913
  • [4] Tomoda C(2015)Cribriform-morular variant of papillary thyroid carcinoma Pathol Res Pract 211 712-716
  • [5] Miyauchi A(2009)Cribriform-morular variant of papillary thyroid carcinoma: molecular characterization of a case with neuroendocrine differentiation and aggressive behavior Am J Clin Pathol 131 134-142
  • [6] Uruno T(2014)Clinicopathological features of rare BRAF mutations in Korean thyroid cancer patients J Korean Med Sci 29 1054-1060
  • [7] Takamura Y(2013)Molecular genotyping of follicular variant of papillary thyroid carcinoma correlates with diagnostic category of fine-needle aspiration cytology: values of RAS mutation testing Thyroid 23 1416-1422
  • [8] Ito Y(2016)Clinical utility of TERT promoter mutations and ALK rearrangement in thyroid cancer patients with a high prevalence of the BRAF V600E mutation Diagn Pathol 11 21-1188
  • [9] Miya A(2015)Cribriform-morular variant of papillary thyroid carcinoma: a study of 3 cases featuring the PIK3CA mutation Hum Pathol 46 1180-208
  • [10] Kobayashi K(2014)Classic papillary thyroid carcinoma with tall cell features and tall cell variant have similar clinicopathologic features Korean J Pathol 48 201-1189