Classification and General Considerations of Thyroid Cancer

Annals of Clinical Pathology Central Review Article *Corresponding author Hiroshi Katoh, Department of Surgery, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, 252-0374, Japan, Tel: 81-42-778-8735; Fax:81-42-778-9556; Email: Classification and General Considerations of Thyroid Cancer Submitted: 22 December 2014 Hiroshi Katoh*, Keishi Yamashita, Takumo Enomoto and Masahiko Watanabe © 2015 Katoh et al. Accepted: 12 March 2015 Published: 13 March 2015 ISSN: 2373-9282 Copyright OPEN ACCESS Department of Surgery, Kitasato University School of Medicine, Japan Keywords Abstract Thyroid cancer is the most common malignancy in endocrine system, composed of four major types; papillary thyroid carcinoma, follicular thyroid carcinoma, anaplastic thyroid carcinoma, and medullary thyroid carcinoma. The incidence of thyroid cancer, especially differentiated thyroid cancer, is increasing in developed countries. Growing body of studies on molecular pathogenesis in thyroid cancer provide clues for further research and diagnostic/therapeutic targets. The general pathological classifications and clinical features of follicular cell derived thyroid carcinomas are overviewed, and recent advances of genetic alterations are discussed in this review. ABBREVIATIONS PTC: Papillary Thyroid Cancer; FTC: Follicular Thyroid Cancer; ATC: Anaplastic Thyroid Cancer; MTC: Medullary Thyroid Cancer; PDTC: Poorly Differentiated Thyroid Cancer; DTC: Differentiated Thyroid Cancer INTRODUCTION Thyroid cancer is the most common malignant disease in endocrine system and is rapidly increasing in incidence [1]. The increasing incidence partially reflects earlier detection of small asymptomatic cancers because of prevalence of screening (i.e., small papillary cancers). However, the incidence has also increased across all tumor sizes and stages [2]. Most of thyroid cancers show biologically indolent phenotype and have an excellent prognosis with survival rates of more than 95% at 20 years although the recurrence or persistent rate is still high [3]. The incidence of thyroid cancer is about three to four times higher among females than males worldwide, ranking the sixth most common malignancy diagnosed in women. Thyroid cancer can occur at any age but it is rare in childhood. Most tumors are diagnosed during third to sixth decade of life. Most primary thyroid cancers are epithelial tumors that originate from thyroid follicular cells. These cancers develop three main pathological types of carcinomas: papillary thyroid carcinoma (PTC), follicular thyroid carcinoma (FTC) and anaplastic thyroid carcinoma (ATC). Medullary thyroid carcinoma (MTC) arises from thyroid parafollicular (C) cells. A histologic classification of thyroid tumors is shown in (Table 1) [4,5]. PTC and FTC are categorized as differentiated thyroid cancer (DTC) because of well differentiation and indolent tumor • Thyroid cancer • Pathological classification • Genetic alteration growth. PTC consists of 85-90% of all thyroid cancer cases, followed by FTC (5-10%) and MTC (about 2%). ATC accounts for less than 2% of thyroid cancers and typically arises in the elder patients. Its incidence continues to rise with age. The mechanism of MTC carcinogenesis is the activation of RET signaling caused by RET mutations [6], which are not observed in follicular thyroid cell derived cancers. Accordingly, this review mainly focuses on follicular thyroid cell derived cancers. The classic treatment for thyroid cancer is conventional thyroidectomy, in part of cases, with adjuvant radioiodine ablation, and most patients can be cured with these treatments. On the other hand, surgically inoperative recurrence, refractoriness to radioiodine in DTC, poorly differentiated thyroid carcinoma and ATC are still lethal diseases. The recent substantial developments in understanding molecular pathogenesis of thyroid cancer have shown promising treatment strategies. In this review, we discuss general pathological characteristics of follicular thyroid cell derived cancers and some recent advancement of molecular pathogenesis. GENERAL AND PATHOLOGICAL FEATURES Papillary carcinoma PTC is a major differentiated adenocarcinoma which consists of 90% of thyroid cancers and shows papillary proliferation pathologically. Most cases have excellent prognosis but approximately 10% of PTC patients undergo recurrences such as lymph node recurrence and lung metastasis. Selecting such high risk patients is the most important challenge as well as treatment of radioiodine refractory PTC. Clinicopathologically, age>45 years, large tumor size, extra thyroidal invasion, distant Cite this article: Katoh H, Yamashita K, Enomoto T, Watanabe M (2015) Classification and General Considerations of Thyroid Cancer. Ann Clin Pathol 3(1): 1045. Email: Katoh et al. (2015) Central Table 1: Thyroid tumors by world health organization (2004). I. Primary 1. Epithelial 2. Non-epithelial A. Follicular cell derived 1) Benign - Follicular adenoma 2) Uncertain malignant potential (UMP) - Hyalinizing trabecular tumor 3) Malignant - Papillary carcinoma - Follicular carcinoma - Poorly differentiated carcinoma - Undifferentiated (Anaplastic) carcinoma B. C cell derived - Medullary carcinoma C. Mixed follicular and C cell derived - Mixed medullary and follicular carcinoma - Mixed medullary and papillary carcinoma D. Epithelial tumors of different or uncertain cell derived - Mucoepidermoid carcinoma - Sclerosing mucoepidermoid carcinoma with eosinophilia - Squamous cell carcinoma - Mucinous carcinoma - Spindle cell tumor with thymus-like differentiation (SETTLE) - Carcinoma showing thymus-like differentiation (CASTLE) - Ectopic thymoma II. Secondary - Primary lymphoma and plasmacytoma - Angiosarcoma - Teratoma - Smooth muscle tumors - Peripheral nerve sheath tumors - Paraganglioma - Solitary fibrous tumor - Follicular dendric cell tumor - Langerhans cell histiocytosis - Rosai-Dorfman disease - Granular cell tumor metastasis, vascular invasion and poor differentiated histology are well known detrimental prognostic factors [4]. PTC is usually gray-white color and shows a variety of gross appearance such as tumors with central scar and infiltrative borders, encapsulated tumor and lesional calcification (Figure 1A). Nearly half of PTCs have multifocal lesions and regional lymph node metastasis. These characteristics do not affect longterm survival [7-9]. Most of PTCs shows papillary growth pattern but nuclear features are more important diagnostic hallmark which are common in almost all cases than such growth pattern itself (Figure 1B) [4]. The nuclear appearances of PTC are clear, ground glass, or Orphan-Annie eyed [10,11]. These nuclei are larger than normal follicular nuclei and overlapping each other. The nuclei contain eosinophilic inclusions and have longitudinal grooves [12]. These nuclear features are important characteristics of PTC but not specific. Indeed, chronic thyroiditis frequently shows similar intranuclear inclusions or nuclear grooves as well as follicular adenoma [4]. Several subtypes are thought to be associated with either favorable or aggressive phenotype although it is still controversial. Here, we discuss about follicular variant, tall cell variant, diffuse sclerosis variant, and solid variant. A certain part of follicular variant of papillary carcinoma (FVPTC) is classified as FTC or follicular adenoma in the past. Ann Clin Pathol 3(1): 1045 (2015) The nuclei of this variant rarely have all of the features of PTC (eg. rare nuclear groove). Accordingly, FVPTCs are often diagnosed as indeterminate cytology in contrast to high diagnostic accuracy of usual PTC. FVPTC is recognized by its follicular structure with papillary cytology, and composed of 2 subtypes; diffuse/invasive (infiltrative) and encapsulated type. FVPTC is associated with favorable prognosis especially if tumor is encapsulated [13]. Diffuse/invasive subtype has similar clinical features to usual PTC. Diagnosis of encapsulated subtype is still under debate since this subtype shows no invasion or incomplete nuclear characteristics. This encapsulated subtype is slowly growing and conservative treatment may be warranted [14]. Tall cell variant composes 10% of PTC, and have a 10-year mortality rate of up to 25%, less favorable prognosis than usual PTC. This variant is often associated with poor prognostic characteristics such as elder age, extra thyroidal invasion, and high mitotic rate. The tall cells are twice as tall as its width, and should occupy >50% of papillary carcinoma cells [4]. The diffuse sclerosis variant is 3% of PTC, which infiltrates the entire thyroid gland and is associated with younger age [15]. Presence of many psammoma bodies is one of hallmark of this variant. Extensive calcification causes exceedingly firm tumor. Background thyroid of this variant shows chronic lymphatic thyroiditis with lymphocytic infiltration, resembling Hashimoto disease [16]. This variant PTC often shows extra thyroidal extension and regional lymph node metastasis at diagnosis, 2/9 Email: Katoh et al. (2015) Central Figure 1 Typical images of papillary thyroid carcinoma Macroscopic (A) (scale bar = 10 mm) and microscopic (B) (H&E, x200) features of PTC. leading to decreased recurrence free survival although mortality is low [17]. Solid variant PTC is diagnosed when solid growth represents more than 50% of tumor. This variant is commonly seen in children and often associated with secondary PTC patients after the Chernobyl nuclear accident [18,19]. Both lymphatic and venous invasion are frequently observed in this variant [20]. Some studies reported that the solid variant is associated with poor prognosis whereas others considered the prognosis of this variant is almost as good as usual PTC [21,22]. Follicular carcinoma FTC represents 5-15% of thyroid cancer with follicular differentiation but no papillary nuclear characteristics [4]. FTC is a solitary encapsulated tumor with gray-tan-pink color, usually focal hemorrhage. FTC is diagnosed by follicular cell invasion of the tumor capsule and/or blood vessels. Vascular invasion leads to worse prognosis than capsular infiltration alone [23]. Majority of FTCs are minimally invasive with slight tumor capsular invasion alone (Figure 2). These minimally invasive FTCs are similar appearance to follicular adenomas and rarely cause distant metastasis [24]. Accordingly, a minimally invasive FTC is difficult to distinguish from a follicular adenoma in cytology or frozen section, and can be diagnosed only after thyroidectomy. Widely invasive FTC is much less common but ~80% of these tumors cause distant metastasis, leading to high mortality rate at around 20% [4]. The poor prognostic factors are distant metastasis, age>45 years, large tumor size, extensive vascular invasion, extra thyroidal extension, and widely invasive tumors [25]. Hürthle cell carcinoma Hürthle cell carcinoma (oxyphilic cell carcinoma) is presumed to be a variant of FTC but its prognosis is thought to be worse than usual FTC [26,27]. A variant of papillary carcinoma is rare and have similar prognosis as FTC [28]. More than 75% follicular cells with oncocytic characteristics are included in Hürthle cell tumor [29]. Oxyphilic or oncocytic cells are characterized by its polygonal shape, eosinophilic granular cytoplasm, hyper chromatic or vesicular nuclei with large nucleolus, and abundant mitochondria. Ann Clin Pathol 3(1): 1045 (2015) Anaplastic carcinoma ATC is extremely aggressive undifferentiated tumor, with almost 100% disease-specific mortality [30], representing about 40% thyroid cancer deaths by only <2% of thyroid cancers. The median survival from diagnosis is around 6 months [31]. ATC extensively invades into surrounding structures, and distant metastases are observed at diagnosis in one-third of ATC patients. Peak age of patients is older than that of DTCs and >70% of patients are women [32]. Approximately 50% of ATC patients have prior or concurrent DTC. It is suggesting that ATC emerges as a result of de-differentiation of DTC. In contrast to DTC, ATC usually does not uptake iodine, leading to refractoriness against radioiodine treatment. Although clinically apparent ATCs are usually unresectable, intrathyroidal ATCs are surgically resectable and such radical resection offers better outcomes [33]. ATC shows extremely invasive large solid tumor with necrosis and hemorrhage (Figure 3). Large, pleomorphic giant cells resembling osteoclasts is one of hallmark of ATC cells [34]. ATC is composed of spindle cells and squamoid cells. Medullary carcinoma MTC represents less than 5% of thyroid carcinomas, which is neuroendocrine tumor originated from C cells of ultimobranchial body of neural crest and secrets calcitonin. Seventy to eighty percent of MTCs are sporadic while 20-30% of MTCs are familial. Familial MTCs are all autosomal dominant inheritance of germ line RET mutations and classified to 3 categories; multiple endocrine neoplasia 2A (MEN2A), multiple endocrine neoplasia 2B (MEN2B), and familial medullary thyroid carcinoma (FMTC) [35]. Peak age of familial MTC is younger (approximately 35 years) that that of sporadic MTC (40-60 years). The overall 5-year survival of patients with MTC is 86%. Poor prognostic factors include older age, advanced stage, the presence of lymph node metastasis at diagnosis, and somatic RET mutation [36]. Sporadic MTC is usually solitary whereas most of familial MTC exhibit bilateral, multicentric foci. MTCs typically exhibit gray-tan color, firm, solid tumors and do not have a well-formed capsule. Tumor includes high concentration of C cells. MTC cells are round to oval, spindle, or polyhedral. Broad fibro vascular bands separate tumors into nodules (Figure 4). The nuclei are round to oval with salt-andpepper nuclear chromatin. Amyloid deposits from calcitonin are 3/9 Email: Katoh et al. (2015) Central Figure 2 Typical images of follicular thyroid carcinoma Gross (scale bar = 10 mm) and microscopic (H&E, x200) images of minimally invasive (A and B) or widely invasive (C and D) FTC Table 2: Genes involved in thyroid follicular cell derived tumors. Genes Type of tumors BRAFV600E (mutation) PTC (usual) RET/PTC (translocation) HRAS, KRAS, NRAS (mutation) FVPTC 15 ATC 25 TCPTC PTC (usual) ATC 0 FA FVPTC 30-50 PTC (usual) 20-40 20-30 0 0-30 PDTC 0 ATC FA PAX8-associated nuclear transcription 25-65 0 0 PTC (usual) <2 ATC 10-20 FTC MAPK and PI3K-AKT 0-20 FVPTC FTC Ann Clin Pathol 3(1): 1045 (2015) 20-25 30-50 ATC MAPK and PI3K-AKT 0-10 FTC PDTC PTEN (mutation) 15-45 0 PDTC MAPK 80-100 FTC PTC (usual) PAX8/PPARγ (translocation) Associated signaling pathways 45 PI3K-AKT 10-15 4/9 Email: Katoh et al. (2015) Central PTEN (deletion) CTNNB1 (mutation) TP53 (mutation) IDH1 (mutation) NDUFA13 (GRIM19) (mutation) FTC 30 ATC 60-70 ATC 70-80 FVPTC 20 ATC 10-30 PDTC PDTC PTC (usual) FTC HCTC PI3K-AKT 25 WNT-β-catenin 25 p53-coupled pathways 10 IDH1-associated metabolic pathways 2-25 15 Mitochondrial function Abbreviations: FVPTC: Follicular Variant PTC; TCPTC: Tall Cell Variant PTC; FA: Follicular Adenoma; PDTC: Poorly Differentiated Thyroid Cancer; HCTC: Hürthle Cell Thyroid Cancer; IDH1: Isocitrate Dehydrogenase 1; NDUFA13: NADH Dehydrogenase (Ubiquinone) 1α Subcomplex 13 frequently present in stroma. A background of C cell hyperplasia is observed in familial but not in sporadic MTCs [37]. Molecular pathogenesis Similarly to other solid cancers, thyroid cancer is initiated by genetic alterations and epigenetic changes in driver oncogenes or tumor suppressor genes [38,39]. Recent advancement of molecular diagnosis in thyroid cancer provides more effective treatment strategies for individual cases. The well known genetic mutation underlying tumorigenesis in thyroid is the activating mutation of RET oncogene in MTC [6]. This RET mutation is not present in thyroid follicular cell derived tumors which represent the most common types of thyroid neoplasms, that is, follicular adenoma and well differentiated papillary and follicular carcinomas. Poorly differentiated and anaplastic carcinomas are considered to develop as a consequence of dedifferentiation of a well differentiated PTC or FTC (Figure 5). In these follicular cell derived cancers, other molecular alterations such as the RAS pathway and the PI3K-AKT pathway are identified in follicular cell derived carcinomas. Here, we focus on the molecular pathogenesis of follicular cell derived carcinoma. (Table 2) demonstrates genetic alterations which have been identified to be involved in thyroid cancer development. Gene mutations BRAF point mutation (T1799A) in exon 15 leads to the expression of BRAF-V600E mutant protein and results in constitutive serine/threonine kinase activation [40,41]. BRAFV600E mutation is one of the most common genetic alteration in thyroid cancer, occurring in approximately 45% (30 to 70%) of sporadic PTC whereas about 15% in follicular variant PTC [42]. Particularly, 80 to 100% of tall cell variant PTC harbor BRAFV600E mutation. BRAFV600E mutation predicts poorer clinical outcomes in PTC, including aggressive pathological features, and higher recurrence rate [43,44]. BRAFV600E mutation is considered to cause loss of radioiodine avidity and consequently refractoriness to radioiodine treatment. RAS point mutation is frequently found in thyroid cancer as well as other solid cancers. Among genes of three RAS isoforms (HRAS, KRAS, and NRAS), NRAS is predominantly mutated in thyroid tumors. RAS mutation is relatively rare (0-20%) in usual PTC whereas almost half of FTC and follicular variant PTC harbor Ann Clin Pathol 3(1): 1045 (2015) RAS mutation [45,46]. RAS mutation is observed in approximately 20% of follicular adenoma, suggesting that RAS mutation is early event in tumorigenesis. RAS mutation dampens GTPase activity, leading to constitutive active state. RAS mutation activates PI3KAKT pathway in thyroid tumorigenesis. Tumor suppressor gene PTEN is a negative regulator of PI3KAKT signaling pathway by opposing function of PI3K. Mutation or deletion of PTEN causes follicular thyroid cell tumorigenesis as well known in Cowden’s disease (syndrome). Cowden’s syndrome is an autosomally inherited disease caused by germ line mutations of the PTEN [47]. Cowden’s disease is a cancer predisposition syndrome closely related to an increased risk of thyroid, breast and endometrial cancers as well as benign hamartomas. Alteration of PTEN is often observed in 40% of FTC overall. Silencing of PTEN by promoter hypermethylation is also found in FTC and ATC [48-50]. Other genes are also mutated in thyroid cancers such as CTNNB1, TP53, IDH1 [51], and NDUFA13 (GRIM19). CTNNB1 is involved in WNT-β-catenin pathway and often mutated in ATC [52]. TP53 encodes tumor suppressor p53 and is involved in a variety of solid cancers. TP53 mutation is frequently observed in ATC (70-80%) [53,54]. Mutations CTNNB1 and TP53 are preferentially observed in ATC or poorly differentiated thyroid carcinoma, suggesting that these genetic alterations may be associated with dedifferentiation or late event in follicular cell derived cancer progression (Figure 5). Although Hürthle cell thyroid cancer does not carry common genetic alterations such as BRAFV600E, RAS or RET/PTC [55], 15% of Hürthle cell thyroid cancer harbor mutations of NDUFA13 (GRIM19) instead [56]. Gene translocations Chromosomal rearrangements of the tyrosine kinase protooncogene RET, specifically RET/PTC rearrangements, are found in 15-45% of usual PTC and 80% of radiation-induced PTC [57,58]. RET is a proto-oncogene encoding receptor tyrosine kinase (RTK). Accordingly, these rearrangements constitutively activate tyrosine kinase, resulting in activation of the MAPK and PI3K-AKT pathways. Among numerous types of RET/PTC translocation, RET/PTC1 (fusion with CCDC6) and RET/PTC3 (fusion with NCOA4) are most common [59,60]. In cases of the Chernobyl accident, RET/PTC3 translocation was commonly observed, then followed by RET/PTC1 translocation with delay [61]. 5/9 Email: Katoh et al. (2015) Central Figure 3 Anaplastic thyroid carcinoma Microscopic images of 2 cases of ATC (H&E, x200). Figure 4 Medullary thyroid carcinoma Macroscopic (A) (scale bar = 10 mm) and microscopic (B) (H&E, x200) features of MTC. RET/PTC BRAFV600E Papillary carcinoma TP53 CTNNB1 PIK3CA Thyroid follicular cells TP53 CTNNB1 PIK3CA Poorly differentiate dcarcinoma TP53 CTNNB1 PIK3CA RAS PAX8/PPARγ Follicular adenoma Anaplastic carcinoma Follicular carcinoma Figure 5 Putative progression steps of thyroid follicular cell derived tumors and associated genetic mutations. Ann Clin Pathol 3(1): 1045 (2015) 6/9 Email: Katoh et al. (2015) Central The paired box 8 (PAX8)/ peroxisome proliferatoractivated receptor γ (PPARG) gene translocation is another common recombinant oncogene in thyroid cancer. PAX8/PPARG translocation is often observed in FTC (25-60%) and follicular variant PTC (∼30%). The PAX8/PPARG fusion protein acts as a dominant-negative inhibitor of wild-type tumor suppressor mechanism of PPARγ [62]. In contrast, the effects of PAX8/PPARG translocation on PAX8 function are still elusive. DNA polymorphisms According to recent advancement in genome-wide analysis, gene variants have been shown to affect on susceptibility to differentiated thyroid cancer (DTC) although it is likely to be low impact on tumorigenesis [63]. DNA polymorphism is a DNA sequence variation occurring commonly with the same population, where the minimum frequency is typically taken as 1%. Associations of DNA polymorphism with DTC are needed to be confirmed. Combined GSTN1-null/GSTT1-null (cytosolic phase II enzyme related genes) genotypes and homozygous carries of the P53 72Pro allele are reported to be associated with a high risk of DTC [64-66]. In the large-scale study in Iceland, two common variants on 9q22.33 and 14q13.3 are associated with DTC [67]. The gene nearest to the 9q22.33 locus is FOXE1 (TTF2) and NKX2-1 (TTF1) is among the genes located at the 14q13.3 locus. These genes encode important transcription factors associated with thyroid functions. Individuals who are homozygous for both variants showed 5.7 fold higher risk of DTC than non-carriers. MicroRNAs MicroRNA (miR) is a small (19-25 nucleotides) non-coding RNA that negatively regulates the expression of coding genes [68]. miRs are considered regulating around 30% of the human genome and may act as tumor suppressor genes or oncogenes [69]. A polymorphism in one miR (miR-146a) and other numerous miRs involved in major signaling pathways (mainly PTEN-PI3K-AKT pathway) are suggested to be important in DTC carcinogenesis [70]. CONCLUSION This review overviews the general pathological features and molecular pathogenesis in follicular cell derived thyroid carcinomas. Recent advances in understanding molecular pathogenesis of thyroid carcinoma give clues to develop novel clinical strategies. However, the mechanisms of tumorigenesis in thyroid remain to be elusive including penetrance of genetic alteration or environmental factors. ACKNOWLEDGEMENTS We thank Kazuya Yamashita for the assistance to collecting pathological images. REFERENCES 1. Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011; 61: 69-90. 2. Enewold L, Zhu K, Ron E, Marrogi AJ, Stojadinovic A, Peoples GE, et al. Rising thyroid cancer incidence in the United States by demographic and tumor characteristics, 1980-2005. Cancer Epidemiol Biomarkers Prev. 2009; 18: 784-791. Ann Clin Pathol 3(1): 1045 (2015) 3. Tuttle RM, Ball DW, Byrd D, Dilawari RA, Doherty GM, Duh QY, et al. Thyroid carcinoma. J Natl Compr Canc Netw. 2010; 8: 1228-1274. 4. DeLellis RA, Lloyd RV, Heitz PU. Pathology and Genetics: Tumors of Endocrine Organs. WHO classification of Tumors. IARC Press, Lyon 2004. 5. Nikiforov YE, Biddinger PW, Thompson LDR. Diagnostic Pathology and Molecular Genetics of the Thyroid. Lippincott Williams & Wilkins 2009. 6. Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, et al. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 1994; 367: 375-376. 7. Cady B. Staging in thyroid carcinoma. Cancer. 1998; 83: 844-847. 8. Hay ID, Bergstralh EJ, Goellner JR, Ebersold JR, Grant CS. Predicting outcome in papillary thyroid carcinoma: development of a reliable prognostic scoring system in a cohort of 1779 patients surgically treated at one institution during 1940 through 1989. Surgery 1993; 114: 1050-7; discussion 7-8. 9. Shaha AR1, Loree TR, Shah JP. Prognostic factors and risk group analysis in follicular carcinoma of the thyroid. Surgery. 1995; 118: 1131-1136. 10. Baloch ZW, LiVolsi VA, Asa SL, Rosai J, Merino MJ, Randolph G, et al. Diagnostic terminology and morphologic criteria for cytologic diagnosis of thyroid lesions: a synopsis of the National Cancer Institute Thyroid Fine-Needle Aspiration State of the Science Conference. Diagn Cytopathol 2008; 36: 425-437. 11. Hapke MR, Dehner LP. The optically clear nucleus. A reliable sign of papillary carcinoma of the thyroid? Am J Surg Pathol. 1979; 3: 31-38. 12. Scopa CD1, Melachrinou M, Saradopoulou C, Merino MJ. The significance of the grooved nucleus in thyroid lesions. Mod Pathol. 1993; 6: 691-694. 13. Tielens ET, Sherman SI, Hruban RH, Ladenson PW. Follicular variant of papillary thyroid carcinoma. A clinicopathologic study. Cancer. 1994; 73: 424-431. 14. Liu J, Singh B, Tallini G, Carlson DL, Katabi N, Shaha A, et al. Follicular variant of papillary thyroid carcinoma: a clinicopathologic study of a problematic entity. Cancer. 2006; 107: 1255-1264. 15. Sherman SI. Thyroid carcinoma. Lancet. 2003; 361: 501-511. 16. Chan JK, Tsui MS, Tse CH. Diffuse sclerosing variant of papillary carcinoma of the thyroid: a histological and immunohistochemical study of three cases. Histopathology. 1987; 11: 191-201. 17. 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: 958-962. 18. Furmanchuk AW, Averkin JI, Egloff B, Ruchti C, Abelin T, Schäppi W, et al. Pathomorphological findings in thyroid cancers of children from the Republic of Belarus: a study of 86 cases occurring between 1986 (‘post-Chernobyl’) and 1991. Histopathology. 1992; 21: 401-408. 19. Nikiforov Y, Gnepp DR, Fagin JA. Thyroid lesions in children and adolescents after the Chernobyl disaster: implications for the study of radiation tumorigenesis. J Clin Endocrinol Metab. 1996; 81: 9-14. 20. Nikiforov Y, Gnepp DR. Pediatric thyroid cancer after the Chernobyl disaster. Pathomorphologic study of 84 cases (1991-1992) from the Republic of Belarus. Cancer 1994; 74: 748-766. 21. Collini P, Mattavelli F, Pellegrinelli A, Barisella M, Ferrari A, Massimino M. Papillary carcinoma of the thyroid gland of childhood and 7/9 Email: Katoh et al. (2015) Central 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: 14201426. 22. 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: 1478-1484. 23. Van Heerden JA, Hay ID, Goellner JR, Salomao D, Ebersold JR, Bergstralh EJ, et al. Follicular thyroid carcinoma with capsular invasion alone: a nonthreatening malignancy. Surgery. 1992; 112: 1130-1136. 24. LiVolsi VA, Asa SL. The demise of follicular carcinoma of the thyroid gland. Thyroid. 1994; 4: 233-236. 25. Ito Y, Hirokawa M, Higashiyama T, Takamura Y, Miya A, Kobayashi K, et al. Prognosis and prognostic factors of follicular carcinoma in Japan: importance of postoperative pathological examination. World J Surg. 2007; 31: 1417-1424. 26. Lopez-Penabad L, Chiu AC, Hoff AO, Schultz P, Gaztambide S, Ordoñez NG, et al. Prognostic factors in patients with Hürthle cell neoplasms of the thyroid. Cancer. 2003; 97: 1186-1194. 27. Sugino K, Ito K, Mimura T, Kameyama K, Iwasaki H, Ito K. Hürthle cell tumor of the thyroid: analysis of 188 cases. World J Surg. 2001; 25: 1160-1163. 28. Herrera MF, Hay ID, Wu PS, Goellner JR, Ryan JJ, Ebersold JR, et al. Hürthle cell (oxyphilic) papillary thyroid carcinoma: a variant with more aggressive biologic behavior. World J Surg. 1992; 16: 669-674. 29. Stojadinovic A, Ghossein RA, Hoos A, Urist MJ, Spiro RH, Shah JP, et al. Hürthle cell carcinoma: a critical histopathologic appraisal. J Clin Oncol. 2001; 19: 2616-2625. 30. Are C, Shaha AR. Anaplastic thyroid carcinoma: biology, pathogenesis, prognostic factors, and treatment approaches. Ann Surg Oncol. 2006; 13: 453-464. 31. Untch BR, Olson JA Jr. Anaplastic thyroid carcinoma, thyroid lymphoma, and metastasis to thyroid. Surg Oncol Clin N Am. 2006; 15: 661-679, x. 32. Kebebew E, Greenspan FS, Clark OH, Woeber KA, McMillan A. Anaplastic thyroid carcinoma. Treatment outcome and prognostic factors. Cancer. 2005; 103: 1330-1335. 33. Sugitani I, Hasegawa Y, Sugasawa M, Tori M, Higashiyama T, Miyazaki M, et al. Super-radical surgery for anaplastic thyroid carcinoma: a large cohort study using the Anaplastic Thyroid Carcinoma Research Consortium of Japan database. Head Neck. 2014; 36: 328-333. 34. Gaffey MJ, Lack EE, Christ ML, Weiss LM. Anaplastic thyroid carcinoma with osteoclast-like giant cells. A clinicopathologic, immunohistochemical, and ultrastructural study. Am J Surg Pathol 1991; 15:160-168. 35. Giuffrida D, Gharib H. Current diagnosis and management of medullary thyroid carcinoma. Ann Oncol. 1998; 9: 695-701. 36. Elisei R, Cosci B, Romei C, Bottici V, Renzini G, Molinaro E, et al. Prognostic significance of somatic RET oncogene mutations in sporadic medullary thyroid cancer: a 10-year follow-up study. J Clin Endocrinol Metab. 2008; 93: 682-687. 37. Etit D, Faquin WC, Gaz R, Randolph G, DeLellis RA, Pilch BZ. Histopathologic and clinical features of medullary microcarcinoma and C-cell hyperplasia in prophylactic thyroidectomies for medullary carcinoma: a study of 42 cases. Arch Pathol Lab Med 2008; 132: 17671773. Ann Clin Pathol 3(1): 1045 (2015) 38. Hanahan D, Weinberg RA. The hallmarks of cancer. Cell 2000; 100: 57-70. 39. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011; 144: 646-674. 40. Cohen Y, Xing M, Mambo E, Guo Z, Wu G, Trink B, et al. BRAF mutation in papillary thyroid carcinoma. J Natl Cancer Inst. 2003; 95: 625-627. 41. Xing M. Molecular pathogenesis and mechanisms of thyroid cancer. Nat Rev Cancer. 2013; 13: 184-199. 42. Xing M. BRAF mutation in thyroid cancer. Endocr Relat Cancer. 2005; 12: 245-262. 43. Xing M, Alzahrani AS, Carson KA, Viola D, Elisei R, Bendlova B, et al. Association between BRAF V600E mutation and mortality in patients with papillary thyroid cancer. JAMA. 2013; 309: 1493-1501. 44. Xing M, Westra WH, Tufano RP, Cohen Y, Rosenbaum E, Rhoden KJ, et al. BRAF mutation predicts a poorer clinical prognosis for papillary thyroid cancer. J Clin Endocrinol Metab. 2005; 90: 6373-6379. 45. Garcia-Rostan G, Zhao H, Camp RL, Pollan M, Herrero A, Pardo J, et al. Ras mutations are associated with aggressive tumor phenotypes and poor prognosis in thyroid cancer. J Clin Oncol. 2003; 21: 3226-3235. 46. Liu Z, Hou P, Ji M, Guan H, Studeman K, Jensen K, et al. Highly prevalent genetic alterations in receptor tyrosine kinases and phosphatidylinositol 3-kinase/akt and mitogen-activated protein kinase pathways in anaplastic and follicular thyroid cancers. J Clin Endocrinol Metab. 2008; 93: 3106-3116. 47. Gustafson S, Zbuk KM, Scacheri C, Eng C. Cowden syndrome. Semin Oncol. 2007; 34: 428-434. 48. Alvarez-Nuñez F, Bussaglia E, Mauricio D, Ybarra J, Vilar M, Lerma E, et al. PTEN promoter methylation in sporadic thyroid carcinomas. Thyroid. 2006; 16: 17-23. 49. Hou P, Ji M, Xing M. Association of PTEN gene methylation with genetic alterations in the phosphatidylinositol 3-kinase/AKT signaling pathway in thyroid tumors. Cancer. 2008; 113: 2440-2447. 50. Schagdarsurengin U, Gimm O, Dralle H, Hoang-Vu C, Dammann R. CpG island methylation of tumor-related promoters occurs preferentially in undifferentiated carcinoma. Thyroid. 2006; 16: 633-642. 51. Murugan AK, Bojdani E, Xing M. Identification and functional characterization of isocitrate dehydrogenase 1 (IDH1) mutations in thyroid cancer. Biochem Biophys Res Commun. 2010; 393: 555-559. 52. Garcia-Rostan G, Tallini G, Herrero A, D’Aquila TG, Carcangiu ML, Rimm DL. Frequent mutation and nuclear localization of beta-catenin in anaplastic thyroid carcinoma. Cancer Res. 1999; 59: 1811-1815. 53. Donghi R, Longoni A, Pilotti S, Michieli P, Della Porta G, Pierotti MA. Gene p53 mutations are restricted to poorly differentiated and undifferentiated carcinomas of the thyroid gland. J Clin Invest. 1993; 91: 1753-1760. 54. Fagin JA, Matsuo K, Karmakar A, Chen DL, Tang SH, Koeffler HP. High prevalence of mutations of the p53 gene in poorly differentiated human thyroid carcinomas. J Clin Invest. 1993; 91: 179-184. 55. Musholt PB, Musholt TJ, Morgenstern SC, Worm K, Sheu SY, Schmid KW. Follicular histotypes of oncocytic thyroid carcinomas do not carry mutations of the BRAF hot-spot. World J Surg. 2008; 32: 722-728. 56. Máximo V, Botelho T, Capela J, Soares P, Lima J, Taveira A, et al. Somatic and germline mutation in GRIM-19, a dual function gene involved in mitochondrial metabolism and cell death, is linked to mitochondrionrich (Hurthle cell) tumours of the thyroid. Br J Cancer. 2005; 92: 18921898. 57. Bounacer A, Wicker R, Caillou B, Cailleux AF, Sarasin A, Schlumberger 8/9 Email: Katoh et al. (2015) Central M, et al. High prevalence of activating ret proto-oncogene rearrangements, in thyroid tumors from patients who had received external radiation. Oncogene. 1997; 15: 1263-1273. 58. Rabes HM, Demidchik EP, Sidorow JD, Lengfelder E, Beimfohr C, Hoelzel D, et al. Pattern of radiation-induced RET and NTRK1 rearrangements in 191 post-chernobyl papillary thyroid carcinomas: biological, phenotypic, and clinical implications. Clin Cancer Res 2000; 6: 1093-1103. 59. Grieco M, Santoro M, Berlingieri MT, Melillo RM, Donghi R, Bongarzone I, et al. PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas. Cell 1990; 60: 557-563. 60. Santoro M, Dathan NA, Berlingieri MT, Bongarzone I, Paulin C, Grieco M, et al. Molecular characterization of RET/PTC3; a novel rearranged version of the RETproto-oncogene in a human thyroid papillary carcinoma. Oncogene 1994; 9: 509-516. 61. Trovisco V, Soares P, Preto A, Castro P, Máximo V, Sobrinho-Simões M. Molecular genetics of papillary thyroid carcinoma: great expectations. Arq Bras Endocrinol Metabol. 2007; 51: 643-653. 62. Placzkowski KA, Reddi HV, Grebe SK, Eberhardt NL, McIver B. The Role of the PAX8/PPARgamma Fusion Oncogene in Thyroid Cancer. PPAR Res 2008; 2008: 672829. 63. Adjadj E, Schlumberger M, de Vathaire F. Germ-line DNA polymorphisms and susceptibility to differentiated thyroid cancer. Lancet Oncol. 2009; 10: 181-190. 64. Canbay E, Dokmetas S, Canbay EI, Sen M, Bardakci F. Higher glutathione transferase GSTM1 0/0 genotype frequency in young thyroid carcinoma patients. Curr Med Res Opin. 2003; 19: 102-106. 65. Granja F, Morari J, Morari EC, Correa LA, Assumpção LV, Ward LS. Proline homozygosity in codon 72 of p53 is a factor of susceptibility for thyroid cancer. Cancer Lett. 2004; 210: 151-157. 66. Morari EC, Leite JL, Granja F, da Assumpção LV, Ward LS. The null genotype of glutathione s-transferase M1 and T1 locus increases the risk for thyroid cancer. Cancer Epidemiol Biomarkers Prev. 2002; 11: 1485-1488. 67. Gudmundsson J, Sulem P, Gudbjartsson DF, Jonasson JG, Sigurdsson A, Bergthorsson JT, et al. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet. 2009; 41: 460-464. 68. Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell. 2009; 136: 215-233. 69. Esquela-Kerscher A, Slack FJ. Oncomirs - microRNAs with a role in cancer. Nat Rev Cancer. 2006; 6: 259-269. 70. De la Chapelle A, Jazdzewski K. MicroRNAs in thyroid cancer. J Clin Endocrinol Metab. 2011; 96: 3326-3336. Cite this article Katoh H, Yamashita K, Enomoto T, Watanabe M (2015) Classification and General Considerations of Thyroid Cancer. Ann Clin Pathol 3(1): 1045. Ann Clin Pathol 3(1): 1045 (2015) View publication stats 9/9