Werner SC. Classification of thyroid disease. Report of the committee on nomenclature. The American Thyroid Association I. J Clin Endocrinol Metab. 1969;29:860–2. https://doi.org/10.1210/jcem-29-6-860.
CAS
CrossRef
PubMed
Google Scholar
Monaco F. Classification of thyroid diseases. In: Monaco F, et al., editors. Thyroid diseases: clinical fundamentals and therapy. Boca Raton, FL: CRC; 1993. p. 3–11.
Google Scholar
Davies TF, Amino N. A new classification for human autoimmune thyroid disease. Thyroid. 1993;3:331–3.
CAS
CrossRef
Google Scholar
Weetman AP. Graves’ disease. N Engl J Med. 2000;343:1236–48.
CAS
CrossRef
Google Scholar
Zhang J, Zhao L, Ga Y, et al. A classification of Hashimoto’s thyroiditis based on immunohistochemistry for IgG4 and IgG. Thyroid. 2014;24:364–70. https://doi.org/10.1089/thy.2013.0211.
CAS
CrossRef
PubMed
Google Scholar
Kottahachchi D, Topliss DJ. Immunoglobulin G4-related thyroid diseases. Eur Thyroid J. 2016;5:231–9. https://doi.org/10.1159/000452623.
CAS
CrossRef
PubMed
PubMed Central
Google Scholar
Mandac JC, Chaudhry S, Sherman KE, Tomer Y. The clinical and physiological spectrum of interferon-alpha induced thyroiditis: toward a new classification. Hepatology. 2006;43:661–72.
CAS
CrossRef
Google Scholar
Mammen JS, Ghazarian SR, Rosen A, Ladenson PW. Patterns of interferon-alpha-induced thyroid dysfunction vary with ethnicity, sex, smoking status, and pretreatment thyrotropin in an international cohort of patients treated for hepatitis C. Thyroid. 2013;23:1151–8. https://doi.org/10.1089/thy.2012.0565.
CAS
CrossRef
PubMed
PubMed Central
Google Scholar
Mammen JS, Ghazarian SR, Pulkstenis E, et al. Phenotypes of interferon-α-induced thyroid dysfunction among patients treated for hepatitis C are associated with pretreatment serum TSH and female sex. J Clin Endocrinol Metab. 2012;97:3270–6. https://doi.org/10.1210/jc.2012-1026.
CAS
CrossRef
PubMed
Google Scholar
Stagnaro-Green A. Approach to the patient with postpartum thyroiditis. J Clin Endocrinol Metab. 2012;97:334–42. https://doi.org/10.1210/jc.2011-2576.
CAS
CrossRef
PubMed
Google Scholar
Takeshima K, Inaba H, Ariyasu H, et al. Clinicopathological features of Riedel’s thyroiditis associated with IgG4-related disease in Japan. Endocr J. 2015;62:725–31. https://doi.org/10.1507/endocrj.EJ15-0175.
CAS
CrossRef
PubMed
Google Scholar
Hennessey JV. Clinical review: Riedel’s thyroiditis: a clinical review. J Clin Endocrinol Metab. 2011;96:3031–41. https://doi.org/10.1210/jc.2011-0617.
CAS
CrossRef
PubMed
Google Scholar
Haugen BR, Nawaz S, Cohn A, et al. Secondary malignancy of the thyroid gland: a case report with review of the literature. Thyroid. 1994;4:297–300.
CAS
CrossRef
Google Scholar
RA DL, Lloyd RV, Heitz PU, et al., editors. World Health Organization classification of tumours. Pathology and genetics of tumours of endocrine organs. Lyon: IARC Press; 2004.
Google Scholar
Shaw JH, Holden A, Sage M. Thyroid lymphoma. Br J Surg. 1989;76:895–7.
CAS
CrossRef
Google Scholar
Tseleni S, Arvanitis D, Kakaviatos N, et al. Primary myxoid chondrosarcoma of the thyroid gland. Arch Pathol Lab Med. 1988;112:94–6.
Google Scholar
Ito Y, Miyauchi A. Prognostic factors and therapeutic strategies for differentiated carcinoma of the thyroid. Endocr J. 2009;56:177–19.2.
CrossRef
Google Scholar
Burgess JR, Tucker P. Incidence trends for papillary thyroid carcinoma and their correlation with thyroid surgery and thyroid fine-needle cytology. Thyroid. 2006;16:47–53.
CrossRef
Google Scholar
Albores-Saavedra J, Henson DE, Glazer E, Schwartz AM. Changing patterns in the incidence and survival of thyroid cancer with follicular phenotype-papillary, follicular and anaplastic: a morphological and epidemiological study. Endocr Pathol. 2007;18:1–7.
CrossRef
Google Scholar
Tallini G, Tuttle RM, Ghossein RA. The history of the follicular variant of papillary thyroid carcinoma. J Clin Endocrinol Metab. 2017;102(1):15–22.
PubMed
Google Scholar
Mete O, Asa SL. Pathological definition and clinical significance of vascular invasion in thyroid carcinomas of follicular epithelial derivation. Med Pathol. 2011;24:1545–52.
CrossRef
Google Scholar
Williams ED. Guest editorial: two proposals regarding the terminology of thyroid tumors. Int J Surg Pathol. 2000;8:181–3.
CrossRef
Google Scholar
Sakamoto A, Kasai A, Sugano H. Poorly differentiated carcinoma of thyroid. A clinicopathologic entity for a high risk group of papillary and follicular carcinomas. Cancer. 1983;52:1849–55.
CAS
CrossRef
Google Scholar
Carcangiu ML, Zampi G, Rosai J. Poorly differentiated (“insular”) thyroid carcinoma. A reinterpretation of Langhans’ “wuchernde Struma”. Am J Surg Pathol. 1984;8:655–68.
CAS
CrossRef
Google Scholar
Volante M, Collini P, Nikiforov YE, et al. Poorly differentiated thyroid carcinoma; the Turin proposal for the use of uniform diagnostic criteria and an algorithmic diagnostic approach. Am J Surg Pathol. 2007;31:1256–64.
CrossRef
Google Scholar
Volante M, Bussolati G, Papotti M. The story of poorly differentiated thyroid carcinoma: from Langhans’ description to the Turin proposal via Juan Rosai. Semin Diagn Pathol. 2016;33:277–83.
CrossRef
Google Scholar
Baloch Z, Livolsi VA, Tondon R. Aggressive variants of follicular cell derived thyroid carcinoma; the so called “real thyroid carcinomas”. J Cin Pathol. 2013;66:733–43.
CrossRef
Google Scholar
Kakudo K, Tang W, Ito Y, et al. Papillary carcinoma of the thyroid in Japan: subclassification of common type and identification of low risk group. J Clin Pathol. 2004;57:1041–6.
CAS
CrossRef
Google Scholar
Bai Y, Kakudo K, Li Y, et al. Subclassification of non-solid type papillary thyroid carcinoma identification of high-risk group in common type. Cancer Sci. 2008;99:1908–15.
CAS
PubMed
Google Scholar
Ito Y, Hirokawa M, Uruno T, et al. Prevalence and biologic behavior of variants of papillary thyroid carcinoma: experience at a single institute. Pathology. 2008;40:617–22.
CrossRef
Google Scholar
Asioli S, Erickson LA, Sebo TJ, et al. Papillary thyroid carcinoma with prominent hobnail features: a new aggressive variant of moderately differentiated papillary carcinoma. Am J Surg Pathol. 2010;34:44–52.
CrossRef
Google Scholar
Kato H, Yamashita K, Enomoto T, et al. Classification and general considerations of thyroid cancer. Ann Clin Pathol. 2015;3:1045–53.
Google Scholar
Sak SD. Variants of papillary thyroid carcinoma: multiple faces of a familiar tumor. Turk Patoloji Derg. 2015;31:34–47.
PubMed
Google Scholar
Motosugi U, Murata S, Nagata K, et al. Thyroid papillary carcinomas with micropapillary and hobnail growth pattern: a histological variant with intermediate malignancy? Thyroid. 2009;19:535–7.
CrossRef
Google Scholar
Lino-Silvia LS, Dominguez-Malagon HR, Caro-Sanchez CH, et al. Thyroid gland papillary Ca with “micropapillary pattern”, a recently recognized poor prognostic finding: clinicopathologic and survival analysis of 7 cases. Hum Pathol. 2012;43:1596–600.
CrossRef
Google Scholar
Sugitani I, Toda K, Yamamoto N, et al. Re-evaluation of histopathological factors affecting prognosis of differentiated thyroid carcinoma in a iodide-sufficient country. World J Surg. 2010;34:1265–73.
CrossRef
Google Scholar
Shi X, Liu R, Basolo F, et al. Differential clinicopathological risk and prognosis of major papillary thyroid cancer variants. J Clin Endocrinol Metab. 2016;101:264–74.
CAS
CrossRef
Google Scholar
Zhu Z, Gandhi M, Nikiforova MN, et al. Molecular profile and clinical- pathologic features of the follicular variant of papillary thyroid carcinoma. An unusually high prevalence of ras mutations. Am J Clin Pathol. 2003;120:71–7.
CAS
CrossRef
Google Scholar
Jung CK, Little MP, Lubin JH, et al. The increase in thyroid cancer incidence during the last four decades is accompanied by a high frequency of BRAF mutations and a sharp increase in RAS mutations. J Clin Endocrinol Metab. 2014;99:276–85.
CrossRef
Google Scholar
Ciampi R, Nikiforov YE. Alterations of the BRAF gene in thyroid tumors. Endocr Pathol. 2005;16:163–72.
CAS
CrossRef
Google Scholar
Nikiforov YE, Seethala RR, Tallini G, et al. Nomenclature revision for encapsulated follicular variant of papillary thyroid carcinoma. JAMA Oncol. 2016;2(8):1023–9.
CrossRef
Google Scholar
Ganly I, Wang L, Tuttle RM, et al. Invasion rather than nuclear features correlates with outcome in encapsulated follicular tumors: further evidence for the reclassification of the encapsulated papillary thyroid carcinoma follicular variant. Hum Pathol. 2015;46:657–64.
CrossRef
Google Scholar
Akslen LA, LiVolsi VA. Prognostic significance of histological grading compared with subclassification of papillary thyroid carcinoma. Cancer. 2000;88:1902–8.
CAS
CrossRef
Google Scholar
Rivera M, Ricarte-Filho J, Patel S, et al. Encapsulated thyroid tumors of follicular cell origin with high grade features (high mitotic rate/tumor necrosis): a clinicopathologic and molecular study. Hum Pathol. 2010;41:172–80.
CAS
CrossRef
Google Scholar
Gnemmi V, Renaud F, DoCao CD, et al. Poorly differentiated thyroid carcinomas: application of Turin proposal provides diagnostic results similar to those from assessment of high-grade features. Histopathology. 2014;64:263–73.
CrossRef
Google Scholar
Xu B, Ibrahimpasic T, Wang L, Sabra MM, et al. Clinicopathologic features of fatal non-anaplastic follicular cell-derived thyroid carcinomas. Thyroid. 2016;26(11):1588–97.
CAS
CrossRef
Google Scholar
Xu B, Wang L, Tuttle RM, Ganly I, Ghossein R. Prognostic impact of extent of vascular invasion in low-grade encapsulated follicular cell-derived thyroid carcinomas: a clinicopathologic study of 276 cases. Hum Pathol. 2015;46:1789–98.
CrossRef
Google Scholar
Stojadinovic A, Ghossein RA, Hoos A, et al. Hurthle cell carcinoma: a critical histopathological appraisal. J Clin Oncol. 2001;19:2616–25.
CAS
CrossRef
Google Scholar
Ito Y, Hirokawa M, Miyauchi A, et al. Diagnostic and surgical indications of oxyphilic follicular tumors in Japan: surgical specimens and cytology. Endocr J. 2016;63(11):977–82.
CAS
CrossRef
Google Scholar
Kakudo K, Bai Y, Katayama S, et al. Classification of thyroid follicular cell tumors of the thyroid gland: analysis involving Japanese patients from one institute. Pathol Int. 2009;59:359–67.
CrossRef
Google Scholar
Kakudo K, Bai Y, Liu Z, et al. Classification of thyroid follicular cell tumors: with special reference to borderline lesions. Endocr J. 2011;59:1–12.
CrossRef
Google Scholar
Kakudo K, Wakasa T, Ohta Z, et al. Prognostic classification of thyroid follicular cell tumors using Ki 67 labelling index risk stratification of thyroid follicular cell carcinomas. Endocr J. 2015;62:1–12.
CrossRef
Google Scholar
Niemeier LA, Kuffner Akatsu H, et al. A combined molecular-pathologic score improves risk stratification of thyroid papillary microcarcinoma. Cancer. 2012;118:2069–77.
CAS
CrossRef
Google Scholar
Wojakowska A, Chekan M, Marczak L, et al. Detection of metabolites discriminating subtypes of thyroid cancer: molecular profiling of FFPE samples using the GC/MS approach. Mol Cell Endocrinol. 2015;417:149–57.
CAS
CrossRef
Google Scholar
Nikiforov YE, Rowland JM, Bove KE, et al. Distinct pattern of ret oncogene rearrangements in morphological variants of radiation-induced and sporadic thyroid papillary carcinomas in children. Cancer Res. 1997;57:1690–4.
CAS
PubMed
Google Scholar
Kimura ET, Nikiforova MN, Zhu Z, et al. High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. Cancer Res. 2003;63:1454–7.
CAS
PubMed
Google Scholar
Giordano TJ, Kuick R, Thomas DG, et al. Molecular classification of papillary thyroid carcinoma: distinct BRAF, RAS and RET/PTC mutation-specific gene expression profiles discovered by DNA microarray analysis. Oncogene. 2005;24:6646–56.
CAS
CrossRef
Google Scholar
Giordano TJ. Follicular cell thyroid neoplasia: insights from genomics and the cancer genome atlas research network. Curr Opin Oncol. 2016;28:1–4.
CAS
CrossRef
Google Scholar
Pratilas CA, Taylor BS, Ye Q, et al. (V600)BRAF is associated with disable feedback inhibition of RAF-MEK signaling and elevated transcriptional output of the pathway. Proc Natl Acad Sci U S A. 2009;106:4519–24.
CAS
CrossRef
Google Scholar
Guerra A, Sapio MR, Marotta V, et al. The primary occurrence of BRAF(V600) is a rare clonal event in papillary thyroid carcinoma. J Clin Endocrinol Metab. 2012;97:517–24.
CAS
CrossRef
Google Scholar
Liu X, Bishop J, Shan Y, et al. Highly prevalent TERT promoter mutations in aggressive thyroid cancers. Endocr Relat Cancer. 2013b;20:603–10.
CrossRef
Google Scholar
Hsiao SJ, Nikiforov YE. Molecular approaches to thyroid cancer diagnosis. Endocr Relat Cancer. 2014;21:301–13.
CrossRef
Google Scholar
Pierlorenzo P, Battista S, Pierantoni GM, Fusco A. Deregulation of micro RNA expression in thyroid neoplasias. Nat Rev Endocrinol. 2014;10:88–101.
CrossRef
Google Scholar
Ito Y, Yoshida H, Maruo R, et al. BRAF mutation in papillary thyroid carcinoma in a Japanese population: its lack of correlation with high-risk clinicopathological features and disease-free survival of patients. Endocr J. 2009;56:89–97.
CAS
CrossRef
Google Scholar
Xing M, Alzahrani AS, Carson KA, Viola D, et al. Association between BRAF V600 mutation and mortality in patients with papillary thyroid cancer. JAMA. 2013;309:1493–501.
CAS
CrossRef
Google Scholar
Torregrossa L, Viola D, Sensi E, et al. Papillary thyroid carcinoma with rare exon 15 BRAF mutation has indolent behavior: a single-institution experience. J Clin Endocrinol Metab. 2016;101:4413–20.
CAS
CrossRef
Google Scholar
Pratilas CA, Solit DB. Therapeutic strategies for targeting BRAF in human cancer. Rev Recent Clin Trials. 2007;2:121–34.
CAS
CrossRef
Google Scholar
Leboeuf R, Baumgartner JE, Benezra M, et al. BRAFV600E mutation is associated with preferential sensitivity to mitogen-activated protein kinase kinase inhibition in thyroid cancer cell lines. J Clin Endocrinol Metab. 2008;93:2194–201.
CAS
CrossRef
Google Scholar
Durante C, Puxeddu E, Ferretti E, et al. BRAF mutations in papillary thyroid carcinomas inhibit genes involved in iodine metabolism. J Clin Endocrinol Metab. 2007;92:2840–3.
CAS
CrossRef
Google Scholar
Farndon JR, Leight GS, Dilley WG, et al. Familial medullary thyroid carcinoma without associated endocrinopathies: a distinct entity. Br J Surg. 1986;73:278–81.
CAS
CrossRef
Google Scholar
Santoro M, Carlomagno F, Romano A, et al. Activation of RET as a dominant transforming gene by germline mutations of MENA and MEN 2B. Science. 1995;267:381–3.
CAS
CrossRef
Google Scholar
Eng C, Clayton D, Schuffenecker I, et al. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. JAMA. 1996;276:1575–9.
CAS
CrossRef
Google Scholar
Machens A, Gimm O, Hinze R, et al. Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties. J Clin Endocrinol Metab. 2001;86:1104–9.
CAS
PubMed
Google Scholar