Endocrinol Metab.  2020 Dec;35(4):696-715. 10.3803/EnM.2020.807.

Updates in the Pathologic Classification of Thyroid Neoplasms: A Review of the World Health Organization Classification

Affiliations
  • 1Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, China
  • 2Department of Pathology and Thyroid Disease Center, Izumi City General Hospital, Izumi, Japan
  • 3Department of Human Pathology, Wakayama Medical University, Graduate School of Medicine, Wakayama, Japan
  • 4Department of Hospital Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea
  • 5Cancer Research Institute, College of Medicine, The Catholic University of Korea, Seoul, Korea

Abstract

Advances in medical sciences and evidence-based medicine have led to momentous changes in classification and management of thyroid neoplasms. Much progress has been made toward avoiding overdiagnosis and overtreatment of thyroid cancers. The new 2017 World Health Organization (WHO) classification of thyroid neoplasms updated the diagnostic criteria and molecular and genetic characteristics reflecting the biology and behavior of the tumors, and newly introduced the category of borderline malignancy or uncertain malignant potential. Some neoplasms were subclassified, renamed, or redefined as a specific entity. This review introduces changes in the fourth edition WHO classification of thyroid tumors and updates the contemporary diagnosis and classification of thyroid tumors. We also discuss several challenges with the proposal of new diagnostic entities, since they have unique histopathologic and molecular features and clinical relevance.

Keyword

Thyroid neoplasms; Classification; Diagnosis; Prognosis; Mutation; Clinical decision-making

Figure

  • Fig. 1 Noninvasive follicular thyroid neoplasm with papillary-like nuclear features. (A) Gross photo showing an encapsulated solid nodule confined to the thyroid gland. (B) Microscopically, the tumor shows a follicular growth pattern. Some follicular cells reveal mild nuclear enlargement, nuclear membrane irregularity, and a pale chromatin pattern which correspond to a nuclear score of 3 (H&E stain, ×400).

  • Fig. 2 Schematic explanation of encapsulated follicular patterned thyroid tumors. NIFTP, noninvasive follicular thyroid neoplasm with papillary-like nuclear features; FV-PTC, follicular variant papillary thyroid carcinoma; FT-UMP, follicular tumor of uncertain malignant potential; WDT-UMP, well-differentiated tumor of uncertain malignant potential; WDC-NOS, well differentiated carcinoma not otherwise specified.

  • Fig. 3 Schematic explanation of encapsulated papillary patterned thyroid tumors. Noninvasive encapsulated papillary patterned thyroid tumors with papillary thyroid carcinoma (PTC)-like nuclear features were not defined in the fourth edition World Health Organization classification of tumors of endocrine organs [2]. Ohba et al. [27] proposed to name it noninvasive encapsulated papillary RAS-like thyroid tumor (NEPRAS). FT-UMP, follicular tumor of uncertain malignant potential; WDT-UMP, well-differentiated tumor of uncertain malignant potential; WDC-NOS, well-differentiated carcinoma not otherwise specified.

  • Fig. 4 Noninvasive encapsulated papillary RAS-like thyroid tumor (NEPRAS). (A) Low-power view of an encapsulated papillary patterned thyroid without capsular or vascular invasion (H&E stain, ×40). (B) Higher magnification reveals mild nuclear enlargement and nuclear membrane irregularity which correspond to a nuclear score of 2 (H&E stain, ×400). Ohba et al. [27] proposed to name this tumor NEPRAS.

  • Fig. 5 Schematic explanation of how to classify four different noninvasive encapsulated thyroid tumors including encapsulated papillary thyroid carcinoma (PTC), noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP), noninvasive encapsulated papillary RAS-like thyroid tumor (NEPRAS), and follicular adenoma. NS, nuclear score.

  • Fig. 6 Hyalinizing trabecular tumor. (A) Tumor cells are arranged in a trabecular pattern and show a spindle shape, abundant cytoplasm, and papillary thyroid carcinoma-like nuclear features (H&E stain, ×400). (B) Fine needle aspiration cytology shows intranuclear pseudoinclusions (arrows) (H&E stain, ×400).

  • Fig. 7 Tall cell variant of papillary thyroid carcinoma (PTC) mixed with classic papillary PTC. (A) The region of tall cells comprises more than 30% of the tumor (H&E stain, ×40). (B) Tall cells are arranged in a “tram-track” parallel pattern and are more than twice as tall as they are wide (H&E stain, ×400).

  • Fig. 8 Columnar cell variant of papillary thyroid carcinoma (PTC). (A) Papillary and glandular architecture lined by columnar cells showing nuclear stratification and lacking characteristic nuclear features of PTC (H&E stain, ×400). (B) Columnar cells resemble secretory-type endometrium having supranuclear cytoplasmic vacuoles (H&E stain, ×400).

  • Fig. 9 Hobnail variant of papillary thyroid carcinoma (PTC) and mimicker. (A) True hobnail variant (H&E stain, ×400). (B) Hobnail-like morphology is often seen in classic PTC with cystic changes (H&E stain, ×400).

  • Fig. 10 Follicular thyroid carcinoma (FTC). (A) Minimally invasive FTC showing capsular invasion only (H&E stain, ×16). (B) A focus of vascular invasion found in an encapsulated angioinvasive FTC (H&E stain, ×253).

  • Fig. 11 Classification of encapsulated thyroid tumors of follicular cell origin according to growth pattern and molecular profiles. Noninvasive encapsulated papillary RAS-like thyroid tumor (NEPRAS) is not currently included as a distinct entity of World Health Organization classification. PTC, papillary thyroid carcinoma; HA, Hürthle cell adenoma; HCC, Hürthle cell carcinoma; FA, follicular adenoma; FTC, follicular thyroid carcinoma; NIFTP, noninvasive follicular thyroid neoplasm with papillary-like nuclear features; iEFVPTC, invasive encapsulated follicular variant of papillary thyroid carcinoma.

  • Fig. 12 Well-differentiated thyroid carcinoma with high-grade features. Papillary thyroid carcinoma showing necrosis (A, H&E stain, ×100) and high proliferative activity with a Ki-67 rate of 18% (B, H&E stain, ×400). Follicular thyroid carcinoma with necrosis (C, H&E stain, ×100) and high mitotic figure (D, H&E stain, ×400). Three mitotic figures (arrows) are noted in one high-power field.

  • Fig. 13 Anaplastic thyroid carcinoma (ATC) associated with papillary thyroid carcinoma (PTC). (A) Left area is ATC and right is PTC (H&E stain, ×100). (B) CD10 immunostain shows a diffuse and strong positivity in ATC (left) and is negative in PTC (right) (×100). (C) High-power view image shows pleomorphic tumor cells (H&E stain, ×400). (D) PAX8 immunostain shows a focal positivity (×400).


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Reference

1. Delellis RA, Lloyd RV, Heitz PU, Eng C. World Health Organization classification of tumours of endocrine organs. 3rd ed. Lyon: International Agency for Research on Cancer (IARC);2004. p. 49–123.
2. Lloyd RV, Osamura RY, Kloppel G, Rosai J. WHO classification of tumours of endocrine organs. 4th ed. Lyon: International Agency for Research on Cancer (IARC);2017. p. 65–143.
3. Williams ED. Guest editorial: two proposals regarding the terminology of thyroid tumors. Int J Surg Pathol. 2000; 8:181–3.
Article
4. Carney JA, Hirokawa M, Lloyd RV, Papotti M, Sebo TJ. Hyalinizing trabecular tumors of the thyroid gland are almost all benign. Am J Surg Pathol. 2008; 32:1877–89.
Article
5. Kakudo K, Bai Y, Liu Z, Li Y, Ito Y, Ozaki T. Classification of thyroid follicular cell tumors: with special reference to borderline lesions. Endocr J. 2012; 59:1–12.
Article
6. Kakudo K, Bai Y, Liu Z, Ozaki T. Encapsulated papillary thyroid carcinoma, follicular variant: a misnomer. Pathol Int. 2012; 62:155–60.
Article
7. Kakudo K, El-Naggar AK, Hodak SP, Khanafshar E, Nikiforov YE, Nose V, et al. Noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) in thyroid tumor classification. Pathol Int. 2018; 68:327–33.
Article
8. Nikiforov YE, Seethala RR, Tallini G, Baloch ZW, Basolo F, Thompson LD, et al. Nomenclature revision for encapsulated follicular variant of papillary thyroid carcinoma: a paradigm shift to reduce overtreatment of indolent tumors. JAMA Oncol. 2016; 2:1023–9.
Article
9. Baloch ZW, Seethala RR, Faquin WC, Papotti MG, Basolo F, Fadda G, et al. Noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP): a changing paradigm in thyroid surgical pathology and implications for thyroid cytopathology. Cancer Cytopathol. 2016; 124:616–20.
Article
10. Bychkov A, Hirokawa M, Jung CK, Liu Z, Zhu Y, Hong SW, et al. Low rate of noninvasive follicular thyroid neoplasm with papillary-like nuclear features in Asian practice. Thyroid. 2017; 27:983–4.
Article
11. Bychkov A, Keelawat S, Agarwal S, Jain D, Jung CK, Hong S, et al. Impact of non-invasive follicular thyroid neoplasm with papillary-like nuclear features on the Bethesda system for reporting thyroid cytopathology: a multi-institutional study in five Asian countries. Pathology. 2018; 50:411–7.
Article
12. Cho U, Mete O, Kim MH, Bae JS, Jung CK. Molecular correlates and rate of lymph node metastasis of non-invasive follicular thyroid neoplasm with papillary-like nuclear features and invasive follicular variant papillary thyroid carcinoma: the impact of rigid criteria to distinguish non-invasive follicular thyroid neoplasm with papillary-like nuclear features. Mod Pathol. 2017; 30:810–25.
Article
13. Akaishi J, Kondo T, Sugino K, Ogimi Y, Masaki C, Hames KY, et al. Prognostic impact of the turin criteria in poorly differentiated thyroid carcinoma. World J Surg. 2019; 43:2235–44.
Article
14. Ibrahim AA, Wu HH. Fine-needle aspiration cytology of noninvasive follicular variant of papillary thyroid carcinoma is cytomorphologically distinct from the invasive counterpart. Am J Clin Pathol. 2016; 146:373–7.
Article
15. Maletta F, Massa F, Torregrossa L, Duregon E, Casadei GP, Basolo F, et al. Cytological features of “noninvasive follicular thyroid neoplasm with papillary-like nuclear features” and their correlation with tumor histology. Hum Pathol. 2016; 54:134–42.
Article
16. Parente DN, Kluijfhout WP, Bongers PJ, Verzijl R, Devon KM, Rotstein LE, et al. Clinical safety of renaming encapsulated follicular variant of papillary thyroid carcinoma: is NIFTP truly benign? World J Surg. 2018; 42:321–6.
Article
17. Rosario PW, Mourao GF. Noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP): a review for clinicians. Endocr Relat Cancer. 2019; 26:R259–66.
Article
18. Seethala RR, Baloch ZW, Barletta JA, Khanafshar E, Mete O, Sadow PM, et al. Noninvasive follicular thyroid neoplasm with papillary-like nuclear features: a review for pathologists. Mod Pathol. 2018; 31:39–55.
Article
19. Strickland KC, Vivero M, Jo VY, Lowe AC, Hollowell M, Qian X, et al. Preoperative cytologic diagnosis of noninvasive follicular thyroid neoplasm with papillary-like nuclear features: a prospective analysis. Thyroid. 2016; 26:1466–71.
Article
20. Thompson LD. Ninety-four cases of encapsulated follicular variant of papillary thyroid carcinoma: a name change to noninvasive follicular thyroid neoplasm with papillary-like nuclear features would help prevent overtreatment. Mod Pathol. 2016; 29:698–707.
Article
21. Thompson LD, Poller DN, Kakudo K, Burchette R, Nikiforov YE, Seethala RR. An international interobserver variability reporting of the nuclear scoring criteria to diagnose noninvasive follicular thyroid neoplasm with papillary-like nuclear features: a validation study. Endocr Pathol. 2018; 29:242–9.
Article
22. Yang GC, Fried KO, Scognamiglio T. Sonographic and cytologic differences of NIFTP from infiltrative or invasive encapsulated follicular variant of papillary thyroid carcinoma: a review of 179 cases. Diagn Cytopathol. 2017; 45:533–41.
23. Hirokawa M, Carney JA, Goellner JR, DeLellis RA, Heffess CS, Katoh R, et al. Observer variation of encapsulated follicular lesions of the thyroid gland. Am J Surg Pathol. 2002; 26:1508–14.
Article
24. Liu Z, Bychkov A, Jung CK, Hirokawa M, Sui S, Hong S, et al. Interobserver and intraobserver variation in the morphological evaluation of noninvasive follicular thyroid neoplasm with papillary-like nuclear features in Asian practice. Pathol Int. 2019; 69:202–10.
Article
25. Lloyd RV, Erickson LA, Casey MB, Lam KY, Lohse CM, Asa SL, et al. Observer variation in the diagnosis of follicular variant of papillary thyroid carcinoma. Am J Surg Pathol. 2004; 28:1336–40.
Article
26. Kakudo K, Liu Z, Bychkov A, Jung CK. Thyroid FNA cytology, differential diagnoses and pitfalls. 2nd ed. Singapore: Springer;2019. Chapter 21, Nuclear features of papillary thyroid carcinoma (BRAF-like tumors), noninvasive follicular thyroid neoplasm with papillary-like nuclear features (RAS-like tumors) and follicular adenoma/follicular thyroid carcinoma (RAS-like tumors). p. 173–9.
27. Ohba K, Mitsutake N, Matsuse M, Rogounovitch T, Nishino N, Oki Y, et al. Encapsulated papillary thyroid tumor with delicate nuclear changes and a KRAS mutation as a possible novel subtype of borderline tumor. J Pathol Transl Med. 2019; 53:136–41.
Article
28. Jung CK, Park SY, Kim JH, Kakudo K. New insights into classification and risk stratification of encapsulated thyroid tumors with a predominantly papillary architecture. J Pathol Transl Med. 2020; 54:197–203.
Article
29. Rosario PW. Noninvasive encapsulated papillary RAS-like thyroid tumor (NEPRAS) or encapsulated papillary thyroid carcinoma (PTC). J Pathol Transl Med. 2020; 54:263–4.
Article
30. Sambade C, Franssila K, Cameselle-Teijeiro J, Nesland J, Sobrinho-Simoes M. Hyalinizing trabecular adenoma: a misnomer for a peculiar tumor of the thyroid gland. Endocr Pathol. 1991; 2:83–91.
Article
31. Nikiforova MN, Nikiforov YE, Ohori NP. GLIS rearrangements in thyroid nodules: a key to preoperative diagnosis of hyalinizing trabecular tumor. Cancer Cytopathol. 2019; 127:560–6.
32. Marchio C, Da Cruz Paula A, Gularte-Merida R, Basili T, Brandes A, da Silva EM, et al. PAX8-GLIS3 gene fusion is a pathognomonic genetic alteration of hyalinizing trabecular tumors of the thyroid. Mod Pathol. 2019; 32:1734–43.
Article
33. Cancer Genome Atlas Research Network. Integrated genomic characterization of papillary thyroid carcinoma. Cell. 2014; 159:676–90.
34. Nikiforova MN, Nikitski AV, Panebianco F, Kaya C, Yip L, Williams M, et al. GLIS rearrangement is a genomic hallmark of hyalinizing trabecular tumor of the thyroid gland. Thyroid. 2019; 29:161–73.
Article
35. Nath MC, Erickson LA. Aggressive variants of papillary thyroid carcinoma: hobnail, tall cell, columnar, and solid. Adv Anat Pathol. 2018; 25:172–9.
Article
36. Ho AS, Luu M, Barrios L, Chen I, Melany M, Ali N, et al. Incidence and mortality risk spectrum across aggressive variants of papillary thyroid carcinoma. JAMA Oncol. 2020; 6:706–13.
Article
37. Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid. 2016; 26:1–133.
Article
38. Song E, Jeon MJ, Oh HS, Han M, Lee YM, Kim TY, et al. Do aggressive variants of papillary thyroid carcinoma have worse clinical outcome than classic papillary thyroid carcinoma? Eur J Endocrinol. 2018; 179:135–42.
Article
39. Limberg J, Ullmann TM, Stefanova D, Buicko JL, Finnerty BM, Zarnegar R, et al. Does aggressive variant histology without invasive features predict overall survival in papillary thyroid cancer?: a national cancer database analysis. Ann Surg. 2019. Oct. 9. [Epub]. https://doi.org/10.1097/SLA.00000-00000003632 .
Article
40. Jung CK. Papillary thyroid carcinoma variants with tall columnar cells. J Pathol Transl Med. 2020; 54:123.
Article
41. Ganly I, Ibrahimpasic T, Rivera M, Nixon I, Palmer F, Patel SG, et al. Prognostic implications of papillary thyroid carcinoma with tall-cell features. Thyroid. 2014; 24:662–70.
Article
42. Wong KS, Higgins SE, Marqusee E, Nehs MA, Angell T, Barletta JA. Tall cell variant of papillary thyroid carcinoma: impact of change in WHO definition and molecular analysis. Endocr Pathol. 2019; 30:43–8.
Article
43. Beninato T, Scognamiglio T, Kleiman DA, Uccelli A, Vaca D, Fahey TJ 3rd, et al. Ten percent tall cells confer the aggressive features of the tall cell variant of papillary thyroid carcinoma. Surgery. 2013; 154:1331–6.
Article
44. Dettmer MS, Schmitt A, Steinert H, Capper D, Moch H, Komminoth P, et al. Tall cell papillary thyroid carcinoma: new diagnostic criteria and mutations in BRAF and TERT. Endocr Relat Cancer. 2015; 22:419–29.
Article
45. Vuong HG, Long NP, Anh NH, Nghi TD, Hieu MV, Hung LP, et al. Papillary thyroid carcinoma with tall cell features is as aggressive as tall cell variant: a meta-analysis. Endocr Connect. 2018; 7:R286–93.
Article
46. Bongers PJ, Kluijfhout WP, Verzijl R, Lustgarten M, Vermeer M, Goldstein DP, et al. Papillary thyroid cancers with focal tall cell change are as aggressive as tall cell variants and should not be considered as low-risk disease. Ann Surg Oncol. 2019; 26:2533–9.
Article
47. Oh WJ, Lee YS, Cho U, Bae JS, Lee S, Kim MH, et al. Classic papillary thyroid carcinoma with tall cell features and tall cell variant have similar clinicopathologic features. Korean J Pathol. 2014; 48:201–8.
Article
48. Rivera M, Ghossein RA, Schoder H, Gomez D, Larson SM, Tuttle RM. Histopathologic characterization of radioactive iodine-refractory fluorodeoxyglucose-positron emission tomography-positive thyroid carcinoma. Cancer. 2008; 113:48–56.
Article
49. Silver CE, Owen RP, Rodrigo JP, Rinaldo A, Devaney KO, Ferlito A. Aggressive variants of papillary thyroid carcinoma. Head Neck. 2011; 33:1052–9.
Article
50. Shi X, Liu R, Basolo F, Giannini R, Shen X, Teng D, et al. Differential clinicopathological risk and prognosis of major papillary thyroid cancer variants. J Clin Endocrinol Metab. 2016; 101:264–74.
Article
51. Villar-Taibo R, Peteiro-Gonzalez D, Cabezas-Agricola JM, Aliyev E, Barreiro-Morandeira F, Ruiz-Ponte C, et al. Aggressiveness of the tall cell variant of papillary thyroid carcinoma is independent of the tumor size and patient age. Oncol Lett. 2017; 13:3501–7.
Article
52. Enriquez ML, Baloch ZW, Montone KT, Zhang PJ, LiVolsi VA. CDX2 expression in columnar cell variant of papillary thyroid carcinoma. Am J Clin Pathol. 2012; 137:722–6.
Article
53. Sujoy V, Pinto A, Nose V. Columnar cell variant of papillary thyroid carcinoma: a study of 10 cases with emphasis on CDX2 expression. Thyroid. 2013; 23:714–9.
Article
54. Yunta PJ, Ponce JL, Prieto M, Merino F, Sancho-Fornos S. The importance of a tumor capsule in columnar cell thyroid carcinoma: a report of two cases and review of the literature. Thyroid. 1999; 9:815–9.
Article
55. Huang WT, Yang SF, Wang SL, Chan HM, Chai CY. Encapsulated columnar-cell carcinoma of the thyroid: a case report. Kaohsiung J Med Sci. 2005; 21:241–4.
Article
56. Chen JH, Faquin WC, Lloyd RV, Nose V. Clinicopathological and molecular characterization of nine cases of columnar cell variant of papillary thyroid carcinoma. Mod Pathol. 2011; 24:739–49.
Article
57. Ieni A, Barresi V, Cardia R, Licata L, Di Bari F, Benvenga S, et al. The micropapillary/hobnail variant of papillary thyroid carcinoma: a review of series described in the literature compared to a series from one southern Italy pathology institution. Rev Endocr Metab Disord. 2016; 17:521–7.
Article
58. Kakudo K, Tang W, Ito Y, Mori I, Nakamura Y, Miyauchi A. Papillary carcinoma of the thyroid in Japan: subclassification of common type and identification of low risk group. J Clin Pathol. 2004; 57:1041–6.
Article
59. Bai Y, Kakudo K, Li Y, Liu Z, Ozaki T, Ito 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.
Article
60. Bai Y, Kakudo K, Nakamura M, Ozaki T, Li Y, Liu Z, et al. Loss of cellular polarity/cohesiveness in the invasive front of papillary thyroid carcinoma and periostin expression. Cancer Lett. 2009; 281:188–95.
Article
61. Asioli S, Erickson LA, Sebo TJ, Zhang J, Jin L, Thompson GB, et al. Papillary thyroid carcinoma with prominent hobnail features: a new aggressive variant of moderately differentiated papillary carcinoma: a clinicopathologic, immunohistochemical, and molecular study of eight cases. Am J Surg Pathol. 2010; 34:44–52.
Article
62. Liu Z, Kakudo K, Bai Y, Li Y, Ozaki T, Miyauchi A, et al. Loss of cellular polarity/cohesiveness in the invasive front of papillary thyroid carcinoma, a novel predictor for lymph node metastasis; possible morphological indicator of epithelial mesenchymal transition. J Clin Pathol. 2011; 64:325–9.
Article
63. Asioli S, Erickson LA, Righi A, Lloyd RV. Papillary thyroid carcinoma with hobnail features: histopathologic criteria to predict aggressive behavior. Hum Pathol. 2013; 44:320–8.
Article
64. Ambrosi F, Righi A, Ricci C, Erickson LA, Lloyd RV, Asioli S. Hobnail variant of papillary thyroid carcinoma: a literature review. Endocr Pathol. 2017; 28:293–301.
Article
65. Lee YS, Kim Y, Jeon S, Bae JS, Jung SL, Jung CK. Cytologic, clinicopathologic, and molecular features of papillary thyroid carcinoma with prominent hobnail features: 10 case reports and systematic literature review. Int J Clin Exp Pathol. 2015; 8:7988–97.
66. Teng L, Deng W, Lu J, Zhang J, Ren X, Duan H, et al. Hobnail variant of papillary thyroid carcinoma: molecular profiling and comparison to classical papillary thyroid carcinoma, poorly differentiated thyroid carcinoma and anaplastic thyroid carcinoma. Oncotarget. 2017; 8:22023–33.
Article
67. Lubitz CC, Economopoulos KP, Pawlak AC, Lynch K, Dias-Santagata D, Faquin WC, et al. Hobnail variant of papillary thyroid carcinoma: an institutional case series and molecular profile. Thyroid. 2014; 24:958–65.
Article
68. Wong KS, Chen TY, Higgins SE, Howitt BE, Lorch JH, Alexander EK, et al. A potential diagnostic pitfall for hobnail variant of papillary thyroid carcinoma. Histopathology. 2020; 76:707–13.
Article
69. Volante M, Collini P, Nikiforov YE, Sakamoto A, Kakudo K, Katoh R, 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.
Article
70. Collini P, Mattavelli F, Pellegrinelli A, Barisella M, Ferrari A, Massimino M. Papillary carcinoma of the thyroid gland of childhood and adolescence: morphologic subtypes, biologic behavior and prognosis: a clinicopathologic study of 42 sporadic cases treated at a single institution during a 30-year period. Am J Surg Pathol. 2006; 30:1420–6.
71. LiVolsi VA, Abrosimov AA, Bogdanova T, Fadda G, Hunt JL, Ito M, et al. The Chernobyl thyroid cancer experience: pathology. Clin Oncol (R Coll Radiol). 2011; 23:261–7.
Article
72. Nikiforov YE, Erickson LA, Nikiforova MN, Caudill CM, Lloyd RV. Solid variant of papillary thyroid carcinoma: incidence, clinical-pathologic characteristics, molecular analysis, and biologic behavior. Am J Surg Pathol. 2001; 25:1478–84.
73. Tronko MD, Bogdanova TI, Komissarenko IV, Epstein OV, Oliynyk V, Kovalenko A, et al. Thyroid carcinoma in children and adolescents in Ukraine after the Chernobyl nuclear accident: statistical data and clinicomorphologic characteristics. Cancer. 1999; 86:149–56.
Article
74. Ohashi R. Solid variant of papillary thyroid carcinoma: an under-recognized entity. Endocr J. 2020; 67:241–8.
Article
75. Ohashi R, Kawahara K, Namimatsu S, Igarashi T, Sakatani T, Sugitani I, et al. Clinicopathological significance of a solid component in papillary thyroid carcinoma. Histopathology. 2017; 70:775–81.
Article
76. Caplan RH, Wester S, Kisken AW. Diffuse sclerosing variant of papillary thyroid carcinoma: case report and review of the literature. Endocr Pract. 1997; 3:287–92.
Article
77. Joung JY, Kim TH, Jeong DJ, Park SM, Cho YY, Jang HW, et al. Diffuse sclerosing variant of papillary thyroid carcinoma: major genetic alterations and prognostic implications. Histopathology. 2016; 69:45–53.
Article
78. Sheu SY, Schwertheim S, Worm K, Grabellus F, Schmid KW. Diffuse sclerosing variant of papillary thyroid carcinoma: lack of BRAF mutation but occurrence of RET/PTC rearrangements. Mod Pathol. 2007; 20:779–87.
Article
79. Pillai S, Gopalan V, Smith RA, Lam AK. Diffuse sclerosing variant of papillary thyroid carcinoma: an update of its clinicopathological features and molecular biology. Crit Rev Oncol Hematol. 2015; 94:64–73.
Article
80. Thompson LD, Wieneke JA, Heffess CS. Diffuse sclerosing variant of papillary thyroid carcinoma: a clinicopathologic and immunophenotypic analysis of 22 cases. Endocr Pathol. 2005; 16:331–48.
Article
81. Koo JS, Hong S, Park CS. Diffuse sclerosing variant is a major subtype of papillary thyroid carcinoma in the young. Thyroid. 2009; 19:1225–31.
Article
82. Fukushima M, Ito Y, Hirokawa M, Akasu H, Shimizu K, Miyauchi A. Clinicopathologic characteristics and prognosis of diffuse sclerosing variant of papillary thyroid carcinoma in Japan: an 18-year experience at a single institution. World J Surg. 2009; 33:958–62.
Article
83. Malandrino P, Russo M, Regalbuto C, Pellegriti G, Moleti M, Caff A, et al. Outcome of the diffuse sclerosing variant of papillary thyroid cancer: a meta-analysis. Thyroid. 2016; 26:1285–92.
Article
84. Kim HJ, Sung JY, Oh YL, Kim JH, Son YI, Min YK, et al. Association of vascular invasion with increased mortality in patients with minimally invasive follicular thyroid carcinoma but not widely invasive follicular thyroid carcinoma. Head Neck. 2014; 36:1695–700.
Article
85. Xu B, Ghossein R. Encapsulated thyroid carcinoma of follicular cell origin. Endocr Pathol. 2015; 26:191–9.
Article
86. O’Neill CJ, Vaughan L, Learoyd DL, Sidhu SB, Delbridge LW, Sywak MS. Management of follicular thyroid carcinoma should be individualised based on degree of capsular and vascular invasion. Eur J Surg Oncol. 2011; 37:181–5.
Article
87. Cracolici V, Ritterhouse LL, Segal JP, Puranik R, Wanjari P, Kadri S, et al. Follicular thyroid neoplasms: comparison of clinicopathologic and molecular features of atypical adenomas and follicular thyroid carcinomas. Am J Surg Pathol. 2020; 44:881–92.
88. Maximo V, Sobrinho-Simoes M. Mitochondrial DNA ‘common’ deletion in Hurthle cell lesions of the thyroid. J Pathol. 2000; 192:561–2.
89. Bishop JA, Wu G, Tufano RP, Westra WH. Histological patterns of locoregional recurrence in Hürthle cell carcinoma of the thyroid gland. Thyroid. 2012; 22:690–4.
Article
90. Haq M, Harmer C. Differentiated thyroid carcinoma with distant metastases at presentation: prognostic factors and outcome. Clin Endocrinol (Oxf). 2005; 63:87–93.
Article
91. Gasparre G, Porcelli AM, Bonora E, Pennisi LF, Toller M, Iommarini L, et al. Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors. Proc Natl Acad Sci U S A. 2007; 104:9001–6.
Article
92. Maximo V, Soares P, Lima J, Cameselle-Teijeiro J, Sobrinho-Simoes M. Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hurthle cell tumors. Am J Pathol. 2002; 160:1857–65.
93. Chindris AM, Casler JD, Bernet VJ, Rivera M, Thomas C, Kachergus JM, et al. Clinical and molecular features of Hurthle cell carcinoma of the thyroid. J Clin Endocrinol Metab. 2015; 100:55–62.
Article
94. Ganly I, Makarov V, Deraje S, Dong Y, Reznik E, Seshan V, et al. Integrated genomic analysis of Hurthle cell cancer reveals oncogenic drivers, recurrent mitochondrial mutations, and unique chromosomal landscapes. Cancer Cell. 2018; 34:256–70.
Article
95. Jung CK, Kim Y, Jeon S, Jo K, Lee S, Bae JS. Clinical utility of EZH1 mutations in the diagnosis of follicular-patterned thyroid tumors. Hum Pathol. 2018; 81:9–17.
Article
96. Sakamoto A, Kasai N, Sugano H. Poorly differentiated carcinoma of the thyroid: a clinicopathologic entity for a high-risk group of papillary and follicular carcinomas. Cancer. 1983; 52:1849–55.
Article
97. Hiltzik D, Carlson DL, Tuttle RM, Chuai S, Ishill N, Shaha A, et al. Poorly differentiated thyroid carcinomas defined on the basis of mitosis and necrosis: a clinicopathologic study of 58 patients. Cancer. 2006; 106:1286–95.
Article
98. Asioli S, Erickson LA, Righi A, Jin L, Volante M, Jenkins S, et al. Poorly differentiated carcinoma of the thyroid: validation of the Turin proposal and analysis of IMP3 expression. Mod Pathol. 2010; 23:1269–78.
Article
99. Bai S, Baloch ZW, Samulski TD, Montone KT, LiVolsi VA. Poorly differentiated oncocytic (Hürthle cell) follicular carcinoma: an institutional experience. Endocr Pathol. 2015; 26:164–9.
Article
100. Ziad el A, Ruchala M, Breborowicz J, Gembicki M, Sowinski J, Grzymislawski M. Immunoexpression of TTF-1 and Ki-67 in a coexistent anaplastic and follicular thyroid cancer with rare long-life surviving. Folia Histochem Cytobiol. 2008; 46:461–4.
101. Kakudo K, Wakasa T, Ohta Y, Yane K, Ito Y, Yamashita H. Prognostic classification of thyroid follicular cell tumors using Ki-67 labeling index: risk stratification of thyroid follicular cell carcinomas. Endocr J. 2015; 62:1–12.
Article
102. Deeken-Draisey A, Yang GY, Gao J, Alexiev BA. Anaplastic thyroid carcinoma: an epidemiologic, histologic, immunohistochemical, and molecular single-institution study. Hum Pathol. 2018; 82:140–8.
Article
103. Dettmer M, Schmitt A, Steinert H, Haldemann A, Meili A, Moch H, et al. Poorly differentiated thyroid carcinomas: how much poorly differentiated is needed? Am J Surg Pathol. 2011; 35:1866–72.
104. Wong KS, Lorch JH, Alexander EK, Marqusee E, Cho NL, Nehs MA, et al. Prognostic significance of extent of invasion in poorly differentiated thyroid carcinoma. Thyroid. 2019; 29:1255–61.
Article
105. Ibrahimpasic T, Ghossein R, Shah JP, Ganly I. Poorly differentiated carcinoma of the thyroid gland: current status and future prospects. Thyroid. 2019; 29:311–21.
Article
106. Bournaud C, Descotes F, Decaussin-Petrucci M, Berthiller J, de la Fouchardiere C, Giraudet AL, et al. TERT promoter mutations identify a high-risk group in metastasis-free advanced thyroid carcinoma. Eur J Cancer. 2019; 108:41–9.
Article
107. Xu B, Ghossein R. Poorly differentiated thyroid carcinoma. Semin Diagn Pathol. 2020; 37:243–7.
Article
108. Keutgen XM, Sadowski SM, Kebebew E. Management of anaplastic thyroid cancer. Gland Surg. 2015; 4:44–51.
109. Kuhn E, Ragazzi M, Ciarrocchi A, Torricelli F, de Biase D, Zanetti E, et al. Angiosarcoma and anaplastic carcinoma of the thyroid are two distinct entities: a morphologic, immunohistochemical, and genetic study. Mod Pathol. 2019; 32:787–98.
Article
110. Talbott I, Wakely PE Jr. Undifferentiated (anaplastic) thyroid carcinoma: practical immunohistochemistry and cytologic look-alikes. Semin Diagn Pathol. 2015; 32:305–10.
Article
111. Bishop JA, Sharma R, Westra WH. PAX8 immunostaining of anaplastic thyroid carcinoma: a reliable means of discerning thyroid origin for undifferentiated tumors of the head and neck. Hum Pathol. 2011; 42:1873–7.
Article
112. Lai WA, Hang JF, Liu CY, Bai Y, Liu Z, Gu H, et al. PAX8 expression in anaplastic thyroid carcinoma is less than those reported in early studies: a multi-institutional study of 182 cases using the monoclonal antibody MRQ-50. Virchows Arch. 2020; 476:431–7.
Article
113. Nakazawa T, Kondo T, Vuong HG, Odate T, Kawai M, Tahara I, et al. High expression of CD10 in anaplastic thyroid carcinomas. Histopathology. 2018; 73:492–9.
Article
114. Oh EJ, Bychkov A, Cho H, Kim TM, Bae JS, Lim DJ, et al. Prognostic implications of CD10 and CD15 expression in papillary thyroid carcinoma. Cancers (Basel). 2020; 12:1413.
Article
115. Xu B, Fuchs T, Dogan S, Landa I, Katabi N, Fagin JA, et al. Dissecting anaplastic thyroid carcinoma: a comprehensive clinical, histologic, immunophenotypic, and molecular study of 360 cases. Thyroid. 2020; 30:1505–17.
Article
116. Leeman-Neill RJ, Kelly LM, Liu P, Brenner AV, Little MP, Bogdanova TI, et al. ETV6-NTRK3 is a common chromosomal rearrangement in radiation-associated thyroid cancer. Cancer. 2014; 120:799–807.
Article
117. Dogan S, Wang L, Ptashkin RN, Dawson RR, Shah JP, Sherman EJ, et al. Mammary analog secretory carcinoma of the thyroid gland: a primary thyroid adenocarcinoma harboring ETV6-NTRK3 fusion. Mod Pathol. 2016; 29:985–95.
Article
118. Stevens TM, Kovalovsky AO, Velosa C, Shi Q, Dai Q, Owen RP, et al. Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study. Mod Pathol. 2015; 28:1084–100.
Article
119. Tirro E, Martorana F, Romano C, Vitale SR, Motta G, Di Gregorio S, et al. Molecular alterations in thyroid cancer: from bench to clinical practice. Genes (Basel). 2019; 10:709.
Article
120. Cocco E, Scaltriti M, Drilon A. NTRK fusion-positive cancers and TRK inhibitor therapy. Nat Rev Clin Oncol. 2018; 15:731–47.
Article
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