Clinicopathological features for predicting central and lateral lymph node metastasis in papillary thyroid microcarcinoma: Analysis of 66 cases that underwent central and lateral lymph node dissection
- Authors:
- Published online on: November 18, 2016 https://doi.org/10.3892/mco.2016.1085
- Pages: 49-55
-
Copyright: © Tao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
The annual incidence of thyroid carcinoma is 6.2% (1) and accounts for 2.7% of all malignant tumor types in females worldwide (2,3). Papillary thyroid microcarcinoma (PTMC), which is defined as a papillary carcinoma with the dimensions equal to or <1.0 cm, according to the World Health Organization classification (4), accounts for 6–35% of thyroid carcinoma and 35.7–61.5% of papillary thyroid carcinoma (PTC) (5–10). PTMC is considered with favorable biological features and good long-term prognosis, as the 10-year disease-specific survival of 99.5% (11). The rate of neck lymph metastasis is 3.1–45.7%, and the sites include level II, III, IV, V, VI (12–14). Lymph node metastasis, particularly central lymph node metastasis (CLNM), is considered to be the most important risk factor associated with recurrence (15–17).
Currently, the surgical approach for PTMC, particularly the ranges of lymph nodes dissection remains controversial (18,19). Although numerous previous studies have suggested that unilateral or bilateral lobectomy, plus prophylactic central lymph node dissection (PCLND; dissection of the level VI lymph nodes which lie in central position of the neck (6,20), including prelaryngeal, pretracheal and paratracheal lymph nodes) for PTMC is enough (21–23), and even overtreatment is performed when no positive lymph nodes were identified in clinical examination (cN0), others still insist that prophylactic lateral lymph node dissection (PLLND) should be performed in certain conditions (24,25). PCLND may cause temporary parathyroid laryngeal damage and injury to laryngeal nerves (26); PLLND may damage accessory nerves, cervical plexus and cause additional complications. Neck ultrasound (US) and contrast-enhanced computed tomography (CT) are widely used for preoperative imaging to visualize the lymph metastasis; unfortunately, both US and contrast-enhanced CT are not particularly accurate, with low sensitivities of 23–53.2 and 41–66.7%, respectively (27,28). Therefore, the risk factors of CLNM and LLNM are important for surgeons to determine the range of neck lymph dissection. Current research demonstrated that age ≥45 years, tumor size >0.5 cm, extrathyroid invasion, multifocality and calcifications were all possible risk factors of CLNM (13,16–20); however, few previous studies have investigated predicting factors of LLNM.
Loss of cellular polarity/cohesiveness (LOP/C) in the invasive front was considered to be a useful morphological feature of the epithelial-mesenchymal transition (EMT) under hematoxylin and eosin staining (29). LOP refers to a phenomenon in which the carcinoma cells are arranged in micropapillary structures with a fibrous axis or irregular tubular patterns, and the nuclei were round and located in the apical cytoplasm, or flat and located centrally (30–32). LOC means that the carcinoma cells were loosely arranged, singly or in small clusters resembling foamy histiocytes or in micropapillary structures (29–32). The invasive front was defined as the interface between the tumor and the adjacent non-neoplastic tissue when the tumor exhibited invasive growth, in which desmoplasia is usually observed (29–32). When LOP/C was definitely present in at least two sites in the invasive front, it is considered to be significant (30). In PTC, LOP/C is associated with increased risk of lymph node metastasis, extrathyroid invasion and aggressive clinical behavior (29); however, the role of LOP/C in PTMC remains to be investigated. In the present study, LOP/C in PTMC was observed and analyzed.
Materials and methods
Patients
The clinical data of 66 patients with PTMC, who underwent unilateral or bilateral lobectomy plus prophylactic cervical lymph node dissections between January 2008 and June 2015 in the Affiliated Hospital of Shandong Medical Sciences (Shandong, China) were retrospectively analyzed. All cases were unilateral lesion and cervical lymph node cN0. The age range was 19–69 years (median, 43.5 years) and the ratio of male:female was 1:4.08. All PTMC patients were confirmed by intraoperative frozen section pathological examination, followed by unilateral or bilateral lobectomy and prophylactic ipsilateral regional lymphadenectomy, including level II, III, IV, V, VI, were performed. Postoperative paraffin section histopathology examinations were performed and pathological features, including subtypes, tumor size, extrathyroidal invasion, multifocality, calcifications, LOP/C, CLNM and LLNM were subjected to a meticulous histopathology examination by two pathologists (Zhiyan Liu and Xiangshan Yang).
Statistical analysis
Fisher's exact test or χ2 test, and binary logistic regression were used to investigate the cases using SPSS software (version 17.0; SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference.
Results
Neck lymph metastasis of 66 PTMC cases
A total of 60.6% (44/66) of cases exhibited neck lymph metastasis, including central and lateral. Only 36.4% (24/66) cases exhibited CLNM and LLNM simultaneously, 13.6% (10/66) have CLNM without LLNM and 9.1% (6/66) have LLNM only. The lymph node metastasis rate of level II, III, IV demonstrated no statistical significance (20, 30.3 and 25.8, respectively, χ2=3.465, P=0.177). Compared with these groups, level VI was higher with a rate of 56.1% (37/66, χ2=25.871, P<0.0001) and level V was lower (4.8%, 3/66, χ2=16.404, P<0.01) (Table I).
Univariate analysis outcome of the high-risk factors of total neck lymph metastasis of PTMC
Univariate analysis revealed that LOP/C was significantly associated with both central or lateral lymph metastasis (P=0.001 and P<0.0001), and the male gender exhibited a statistical significant difference compared with female in CLNM (76.9 vs. 45.3%, P=0.04), while the age <45 years, tumor size >0.5 cm and multifocality were high-risk factors of LLNM (P=0.022, 0.044 and 0.005, respectively). Extrathyroid invasion and calcifications were demonstrated to be not statistically significant with CLNM and LLNM (Table II).
The data of binary logistic regression for outcome of the central and lateral lymph metastasis risk factors of PTMC revealed that LOP/C was significantly associated with CLNM (P=0.007) and LLNM (P=0.029) (Tables III and IV). Both multivariable analysis and χ2 test revealed that CLNM was another important risk factor of LLNM (P=0.021; Table IV) (χ2=17.867, P<0.001, Table V). Gender, age, subtypes, extrathyroid invasion, multifocality and calcifications faile to reach statistical significance for either CLNM or LLNM (Tables III and IV).
Table III.Multivariable analysis of risk factors for papillary thyroid microcarcinoma central lymph node metastasis. |
Table IV.Multivariable analysis of risk factors for papillary thyroid microcarcinoma lateral lymph node metastasis. |
Discussion
The male gender and an age ≥45 have been consistently recognized as independent risk factors of lymph metastasis in thyroid carcinoma (33). However, in PTMC, this view is remains controversial. The result of Zhao et al (34) shows male gender and age ≥45 are at a higher risk of lymph node metastasis; however, certain other previous studies demonstrated that no statistically significant association existed between them (20,34,35). The research of 1,990 PTMC cases reported that the male incidence of thyroid carcinoma was associated with absence of environment protection mechanisms and emphasized that surgical intervention may possibly improve male's prognosis (36). An age ≥45 is commonly considered as a risk factor for tumor recurrence and lymph node metastasis, however, other literature has suggested that adolescents tend to develop neck lymph node metastasis (35–37). The univariate analysis revealed that male gender tended to associate more with CLNM (10/13, 76.9%, P=0.04) and patients <45 years were more at risk of LLNM (18/33, 54.5%, P=0.022). However, in the multivariate analysis, these factors failed to reach statistical significance (Tables III and IV).
Tumor size >0.5 cm is also recognized as a risk factor for lymph node metastasis in PTMC (17,35). PTMC with size >0.5 cm may be associated with more vascular and extrathyroid invasion, more incidence in females and more CLNM (38). Lee et al (39) demonstrated that PTMC CLNM of tumor size ≤0.5 cm compared with size >0.5 cm was 18.2 vs. 29.2% (P=0.018), and LLNM was only 5.5% (39). The present univariate analysis results revealed more LLNM of PTMC >0.5 cm (53.1 vs. 29.4%, P=0.044); however, it still failed to reach statistical significance in the multivariate analysis.
A total of 5 subtypes were found in the 66 cases, according to pathological features (40): Classical papillary variant (CPV), unclassical papillary variant (UCPV), follicular variant (FCV), tall cell variant (TCV) and diffuse sclerosing variant (DSV). TCV and DSV were considered as aggressive variants (41) and tend to exhibit more aggressive pathological characteristics, including higher rates of extrathyroidal extension compared with classic PTMC, more multifocality in TCV and more lymph metastasis in DSV; however, the survival appears to be similar (42). In the present study, CLNM and LLNM exhibited no statistically significant difference between each subtype, and subtype was not a high risk factor of CLNM and LLNM (P=0.251 and 0.381, respectively; Tables III and IV). However, due to a reduced number of DSV and TSV, further research is required.
Extrathyroid invasion, multifocality and calcification are all valuable high-risk factors of lymph metastasis of PTMC (43–45). PTMC with these pathological characters exhibit more aggressive biological behavior (42). Multifocality was considered the intraglandular spread of the primary tumor, which indicated the tumor cells were apt to shed off from primary lesion and distribute in thyroid (46,47). When the primary lesion penetrated the fibrous capsule of thyroid, the tumor cells metastasized easier without the restrain of the capsule (29). Shindo et al (44) and Chow et al (48) reported that neck lymph node metastasis was significantly correlated with tumor multifocality. Multiple microcalcifications were recognized as an important feature of malignancy, and PTMC with calcification was detected with a large size and higher lymph node ratio compared with non-calcified lesions (45). Unfortunately, these options remain controversial (34,38). The present univariate analysis result revealed that multifocality was a significant high-risk factor for LLNM, however, in the multivariate analysis, they were not significant.
The EMT is a crucial step in the process of migration of carcinoma tumors from the primary site into surrounding tissues (49–51), which features a loss of epithelial properties and the acquisition of mesenchymal properties, including the loss of apical-basal polarity, loss of cell-cell adhesion, loss of E-cadherin expression, and overexpression of vimentin, epidermal growth factor receptor (EGFR), matrix metalloproteinase-9, TGF-β, NFκb and integrin pathway members in the invasive front (52,53). However, the affirmation of the EMT requires examination of biomarkers, including E-cadherin, N-cadherin, vimentin and fibronectin (53,54). LOP/C in the invasive front is considered to be a be a useful morphological feature of the EMT, and can be observed directly under hematoxylin and eosin staining, without immunohistochemical examination (29). PTCs with LOP/C was significantly correlated with poor clinical outcome as extrathyroid invasion and lymph node metastasis more frequently, and the majority exhibited extrathyroid invasion and were in an advanced tumor stage at surgery (29–32). The present research revealed that in PTMC, more multifocality (20/23 vs. 18/43, χ2=12.476, P<0.0001), CLNM and LLNM were more observed in the cases with LOP/C compared with the cases without (Table II), which proved that the invasive capacity of tumor was enhanced, and LOP/C was confirmed to be a high-risk factor of CLNM and LLNM (P=0.007 and 0.029, respectively; Tables III and IV).
PCLND is recommended as the standard treatment of PTMC; however, the controversy has never ceased. Certain surgeons advocate that PCLND must not be recommended to patients with PTMC, for its reduced malignancy, and PCLND may cause perioperative side effect, including hypoparathyroidism and laryngeal nerve injury (55,56). Additionally, CLNM does not affect the PTMC prognosis (57), even with re-operation following recurrence (58). By contrast, other clinicians suggest that PCLND can reduce the recurrence and improve the survival (59,60). Previous research has revealed that CLNM of PTMC, without risk factors such as male gender, age ≥45, extrathyroid invasion, multifocality and aggressive subtype, was only 6.80–8.13% and PCLND was not recommend (20,36). On the contrary, PCLND was necessary in PTMC with these factors (13,25). However, in the present study, the high risk factors of CLNM were male gender and LOP/C (Tables III and IV). A total of 56.1% (37/66) of patients exhibited CLNM, while the rate of CLNM with male gender and LOP/C was 87.0% (20/23) compared with 32.5% (14/43) in patients without these factors (χ2=10.267, P<0.001). These data indicate that PCLND may be necessary for PTMC, regardless of the high risk factors.
PLLND of PTMC has not been emphasized due to of the low incidence of LLNM; for example, 5.5% (39) and less effect on the survival (23). However, Zeng et al (25) found that the rate of LLNM was 30.5% (43/141) and the number of positive central lymph node ≥2, accompanying with Hashimoto's thyroiditis and extrathyroidal extension were the independent predictive factors for LLNM (25). Another analysis revealed that the presence of CLNM, upper third location of malignancy and tumor size were independent factors for predicting LLNM (61). The present result demonstrated that 45.5% (30/66) cases exhibited LLNM and the ratio of II, III, IV, V was 20, 30.3, 25.8 and 4.8%, respectively. A total of 70.6% (24/34) of the cases with CLNM had LLNM and it was significantly higher compared with the 18.8% (6/32) of the cases without CLNM (χ2=17.867, P<0.001; Table V), and the ratio was 81.8% (18/22) when the number of CLNM ≥2. CLNM and LOP/C were high-risk factors of LLNM in both univariate and multivariate analyses; The rate of LLNM was 83.3% (15/18) when LOP/C and CLNM existed simultaneously. An age <45 years, tumor size >0.5 cm and multifocality were significant in the univariate analysis. The rate of LLND in PTMC without age <45 years, tumor size >0.5 cm, multifocality, LOP/C and CLNM was 0% (0/9). In the factors mentioned above, CLNM and LOP/C were important and useful since intraoperative frozen section pathological examination can confirm them and assist the surgeon to make the decision whether PLLND should be performed, even though no evidence suggests that a level IV node is the sentinel of II, III, IV or V in anatomy, and the mechanism remains unclear.
According to the present results, CLNM tends to occur in patients with male gender and LOP/C, while LLNM is more likely to be associated with age <45 years, tumor size >0.5 cm, multifocality, LOP/C and CLNM. PTMC is not an occult cancer and it can act like larger PTC (62). Currently, no effective preoperative examination exists to confirm the existence of LLNM, when clinical examination of cervical lymph node is negative. The present results revealed that 45.5% (30/66) of cases had LLNM and the ratio of II, III, IV and V was 20, 30.3, 25.8 and 4.8%, respectively; therefore, it may not be enough for certain PTMC patients if only CLNM is performed. Therefore, intraoperative frozen section pathological examination of high-risk factors will be useful to direct the surgical approach of PTMC and reduce the regional recurrence. PLLND is recommend intensely if LOP/C and CLNM are performed by intraoperative frozen section pathological examination and must be considered in patients with the age <45 years, tumor size >0.5 cm and multifocal lesions.
Acknowledgements
The authors would like to thank Professor Zhiyan Liu (Department of Pathology, Qilu Hospital, Shandong, China) for suggesting the direction of pathological examination for us. The present study was supported by the subject of Shandong Province Science and Technology Office, ‘Research of relationship between pathological subtypes of papillary thyroid microcarcinoma and cervical lymph node metastasis’ (no. 2013YD18034).
References
Jemal A, Siegel R, Ward E, Hao Y, Xu J and Thun MJ: Cancer statistics, 2009. CA Cancer J Clin. 59:225–249. 2009. View Article : Google Scholar : PubMed/NCBI | |
Lundgren CI, Hall P, Dickman PW and Zedenius J: Clinically significant prognostic factors for differentiated thyroid carcinoma: A population-based, nested case-control study. Cancer. 106:524–531. 2006. View Article : Google Scholar : PubMed/NCBI | |
Ferlay J, Shin HR, Bray F, Forman D, Mathers C and Parkin DM: Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 127:2893–2917. 2010. View Article : Google Scholar : PubMed/NCBI | |
Sobin LH: Histological typing of thyroid tumours. Histopathology. 16:5131990. View Article : Google Scholar : PubMed/NCBI | |
Lee J, Song Y and Soh EY: Central lymph node metastasis is an important prognostic factor in patients with papillary thyroid microcarcinoma. J Korean Med Sci. 29:48–52. 2014. View Article : Google Scholar : PubMed/NCBI | |
American Thyroid Association (ATA) Guidelines Taskforce on Thyroid Nodules and Differentiated Thyroid Cancer, ; Cooper DS, Doherty GM, Haugen BR, Kloos RT, Lee SL, Mandel SJ, Mazzaferri EL, McIver B, Pacini F, et al: Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 19:1167–1214. 2009. View Article : Google Scholar : PubMed/NCBI | |
Pfister DG, Spencer S, Brizel DM, Burtness B, Busse PM, Caudell JJ, Cmelak AJ, Colevas AD, Dunphy F, Eisele DW, et al: Head and neck cancers, Version 2.2014. Clinical practice guidelines in oncology. J Natl Compr Canc Netw. 12:1454–1487. 2014.PubMed/NCBI | |
Yoshida A: Guidelines for the management of thyroid tumors. Nihon Geka Gakkai Zasshi. 113:507–601. 2012.(In Japanese). PubMed/NCBI | |
Teng W, Liu YF, Gao M and Huang G: Management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Chin J Clin Oncol. 17:1249–1272. 2012. | |
Chen Q, Zou XH, Wei T, Huang QS, Sun YH and Zhu JQ: Prediction of ipsilateral and contralateral central lymph node metastasis in unilateral papillary thyroid carcinoma: A retrospective study. Gland Surg. 4:288–294. 2015.PubMed/NCBI | |
Kuo EJ, Goffredo P, Sosa JA and Roman SA: Aggressive variants of papillary thyroid microcarcinoma are associated with extrathyroidal spread and lymph-node metastases: A population-level analysis. Thyroid. 23:1305–1311. 2013. View Article : Google Scholar : PubMed/NCBI | |
Kebebew E: Heraditary non-medullary thyroid cancer. World J Surg. 32:678–682. 2008. View Article : Google Scholar : PubMed/NCBI | |
Yang Y, Chen C, Chen Z, Jiang J, Chen Y, Jin L, Guo G, Zhang X and Ye T: Prediction of central compartment lymph node metastasis in papillary thyroid microcarcinoma. Clin Endocrinol (Oxf). 81:282–288. 2014. View Article : Google Scholar : PubMed/NCBI | |
Nam-Goong IS, Kim HY, Gong G, Lee HK, Hong SJ, Kim WB and Shong YK: Ultrasonography-guided fine-needle aspiration of thyroid incidentaloma: Correlation with pathological findings. Clin Endocrinol (Oxf). 60:21–28. 2004. View Article : Google Scholar : PubMed/NCBI | |
Hay ID, Hutchinson ME, Gonzalez-Losada T, McIver B, Reinalda ME, Grant CS, Thompson GB, Sebo TJ and Goellner JR: Papillary thyroid microcarcinoma: A study of 900 cases observed in a 60-year period. Surgery. 144:980–988. 2008. View Article : Google Scholar : PubMed/NCBI | |
Pisanu A, Reccia I, Nardello O and Uccheddu A: Risk factors for nodal metastasis and recurrence among patients with papillary thyroid microcarcinoma: Differences in clinical relevance between nonincidental and incidental tumors. World J Surg. 33:460–468. 2009. View Article : Google Scholar : PubMed/NCBI | |
Usluogullari CA, Onal ED, Ozdemir E, Ucler R, Kiyak G, Ersoy PE, Yalcin S, Güler G, Ersoy R and Cakir B: A retrospective analysis of prognostic factors predictive of lymph-node metastasis and recurrence in thyroid papillary microcarcinoma. Minerva Endocrinol. 40:15–22. 2015.PubMed/NCBI | |
Giordano D, Gradoni P, Oretti G, Molina E and Ferri T: Treatment and prognostic factors of papillary thyroid microcarcinoma. Clin Otolaryngol. 35:118–124. 2010. View Article : Google Scholar : PubMed/NCBI | |
Garrel R, Tripodi C, Cartier C, Makeieff M, Crampette L and Guerrier B: Cervical lymphadenopathies signaling thyroid microcarcinoma. Case study and review of the literature. Eur Ann Otorhinolaryngol Head Neck Dis. 128:115–119. 2011. View Article : Google Scholar : PubMed/NCBI | |
Liu Z, Wang L, Yi P, Wang CY and Huang T: Risk factors for central lymph node metastasis of patients with papillary thyroid microcarcinoma: A meta-analysis. Int J Clin Exp Pathol. 7:932–937. 2014.PubMed/NCBI | |
De Pasquale L, Bastagli A, Moro GP and Ghilardi G: Thyroid microcarcinoma approach: A ten year experience. Ann Ital Chir. 84:533–539. 2013.PubMed/NCBI | |
Pedrazzini L, Baroli A, Marzoli L, Guglielmi R and Papini E: Cancer recurrence in papillary thyroid microcarcinoma: A multivariate analysis on 231 patients with a 12-year follow-up. Minerva Endocrinol. 38:269–279. 2013.PubMed/NCBI | |
Karatzas T, Vasileiadis I, Kapetanakis S, Karakostas E, Chrousos G and Kouraklis G: Risk factors contributing to the difference in prognosis for papillary versus micropapillary thyroid carcinoma. Am J Surg. 206:586–593. 2013. View Article : Google Scholar : PubMed/NCBI | |
Shin HJ, Kim EK, Moon HJ, Yoon JH, Han KH and Kwak JY: Can increased tumoral vascularity be a quantitative predicting factor of lymph node metastasis in papillary thyroid microcarcinoma? Endocrine. 47:273–282. 2014. View Article : Google Scholar : PubMed/NCBI | |
Zeng RC, Zhang W, Gao EL, Cheng P, Huang GL, Zhang XH and Li Q: Number of central lymph node metastasis for predicting lateral lymph node metastasis in papillary thyroid microcarcinoma. Head Neck. 36:101–106. 2014. View Article : Google Scholar : PubMed/NCBI | |
Khairy GA and Al-Saif A: Incidental parathyroidectomy during thyroid resection: Incidence, risk factors, and outcome. Ann Saudi Med. 31:274–278. 2011. View Article : Google Scholar : PubMed/NCBI | |
Choi JS, Kim J, Kwak JY, Kim MJ, Chang HS and Kim EK: Preoperative staging of papillary thyroid carcinoma: Comparison of ultrasound imaging and CT. AJR Am J Roentgenol. 193:871–878. 2009. View Article : Google Scholar : PubMed/NCBI | |
Hwang HS and Orloff LA: Efficacy of preoperative neck ultrasound in the detection of cervical lymph node metastasis from thyroid cancer. Laryngoscope. 121:487–491. 2011. View Article : Google Scholar : PubMed/NCBI | |
Liu Z, Kakudo K, Bai Y, Li Y, Ozaki T, Miyauchi A, Taniguchi E and Mori I: 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. 64:325–329. 2011. View Article : Google Scholar : PubMed/NCBI | |
Bai Y, Kakudo K, Li Y, Liu Z, Ozaki T, Ito Y, Kihara M and Miyauchi A: Subclassification of non-solid-type papillary thyroid carcinoma identification of high-risk group in common type. Cancer Sci. 99:1908–1915. 2008.PubMed/NCBI | |
Kakudo K, Tang W, Ito Y, Mori I, Nakamura Y and Miyauchi A: Papillary carcinoma of the thyroid in Japan: Subclassification of common type and identification of low risk group. J Clin Pathol. 57:1041–1046. 2004. View Article : Google Scholar : PubMed/NCBI | |
Tang W, Nakamura Y, Zuo H, Yasuoka H, Yang Q, Wang X, Nakamura M, Mori I, Miyauchi A and Kakudo K: Differentiation, proliferation and retinoid receptor status of papillary carcinoma of the thyroid. Pathol Int. 53:204–213. 2003. View Article : Google Scholar : PubMed/NCBI | |
Koo BS, Choi EC, Yoon YH, Kim DH, Kim EH and Lim YC: Predictive factors for ipsilateral or contralateral central lymph node metastasis in unilateral papillary thyroid carcinoma. Ann Surg. 249:840–844. 2009. View Article : Google Scholar : PubMed/NCBI | |
Zhao Q, Ming J, Liu C, Shi L, Xu X, Nie X and Huang T: Multifocality and total tumor diameter predict central neck lymph node metastases in papillary thyroid microcarcinoma. Ann Surg Oncol. 20:746–752. 2013. View Article : Google Scholar : PubMed/NCBI | |
Ghossein R, Ganly I, Biagini A, Robenshtok E, Rivera M and Tuttle RM: Prognostic factors in papillary microcarcinoma with emphasis on histologic subtyping: A clinicopathologic study of 148 cases. Thyroid. 24:245–253. 2014. View Article : Google Scholar : PubMed/NCBI | |
Lu ZZ, Zhang Y, Wei SF, Li DS, Zhu QH, Sun SJ, Li M and Li LI: Outcome of papillary thyroid microcarcinoma: Study of 1,990 cases. Mol Clin Oncol. 3:672–676. 2015.PubMed/NCBI | |
Handkiewicz-Junak D, Włoch J, Czarniecka A, Roskosz J, Prokurat A, Pomorski L, Krajewska J, Kropińska A, Kukulska A and Jarzab B: Completion total thyroidectomy in children with differentiated thyroid cancer. Endokrynol Pol. 57:356–361. 2006.(In Polish). PubMed/NCBI | |
Kim E, Choi JY, Koo do H, Lee KE and Youn YK: Differences in the characteristics of papillary thyroid microcarcinoma ≤5 mm and >5 mm in diameter. Head Neck. 37:694–697. 2015. View Article : Google Scholar : PubMed/NCBI | |
Lee HS, Park HS, Kim SW, Choi G, Park HS, Hong JC, Lee SG, Baek SM and Lee KD: Clinical characteristics of papillary thyroid microcarcinoma less than or equal to 5 mm on ultrasonography. Eur Arch Otorhinolaryngol. 270:2969–2974. 2013. View Article : Google Scholar : PubMed/NCBI | |
DeLellis RA, Lloyd RV, Heitz PU and Eng C: World Health Organization Classification of TumoursPathology and Genetics of Tumours of Endocrine Organs. IARC Press; Lyon: pp. 57–103. 2004 | |
Silver CE, Owen RP, Rodrigo JP, Rinaldo A, Devaney KO and Ferlito A: Aggressive variants of papillary thyroid carcinoma. Head Neck. 33:1052–1059. 2011. View Article : Google Scholar : PubMed/NCBI | |
Kuo EJ, Goffredo P, Sosa JA and Roman SA: Aggressive variants of papillary thyroid microcarcinoma are associated with extrathyroidal spread and lymph-node metastases: A population-level analysis. Thyroid. 23:1305–1311. 2013. View Article : Google Scholar : PubMed/NCBI | |
Chung YS, Kim JY, Bae JS, Song BJ, Kim JS, Jeon HM, Jeong SS, Kim EK and Park WC: Lateral lymph node metastasis in papillary thyroid carcinoma: Results of therapeutic lymph node dissection. Thyroid. 19:241–246. 2009. View Article : Google Scholar : PubMed/NCBI | |
Shindo M, Wu JC, Park EE and Tanzella F: The importance of central compartment elective lymph node excision in the staging and treatment of papillary thyroid cancer. Arch Otolaryngol Head Neck Surg. 132:650–654. 2006. View Article : Google Scholar : PubMed/NCBI | |
Oh EM, Chung YS, Song WJ and Lee YD: The pattern and significance of the calcifications of papillary thyroid microcarcinoma presented in preoperative neck ultrasonography. Ann Surg Treat Res. 86:115–121. 2014. View Article : Google Scholar : PubMed/NCBI | |
Mazeh H, Samet Y, Hochstein D, Mizrahi I, Ariel I, Eid A and Freund HR: Multifocality in well-differentiated thyroid carcinomas calls for total thyroidectomy. Am J Surg. 201:770–775. 2011. View Article : Google Scholar : PubMed/NCBI | |
Sun W, Lan X, Zhang H, Dong W, Wang Z, He L, Zhang T and Liu S: Risk factors for central lymph node metastasis in CN0 papillary thyroid carcinoma: A Systematic Review and Meta-Analysis. PLoS One. 10:e01390212015. View Article : Google Scholar : PubMed/NCBI | |
Chow SM, Law SC, Chan JK, Au SK, Yau S and Lau WH: Papillary microcarcinoma of the thyroid-prognostic significance of lymph node metastasis and multifocality. Cancer. 98:31–40. 2003. View Article : Google Scholar : PubMed/NCBI | |
Christofori G: New signals from the invasive front. Nature. 441:444–450. 2006. View Article : Google Scholar : PubMed/NCBI | |
Sánchez-Tilló E, Liu Y, de Barrios O, Siles L, Fanlo L, Cuatrecasas M, Darling DS, Dean DC, Castells A and Postigo A: EMT-activating transcription factors in cancer: Beyond EMT and tumor invasiveness. Cell Mol Life Sci. 69:3429–3456. 2012. View Article : Google Scholar : PubMed/NCBI | |
Cheng Y and Cu QC: Research advances in epithelial-mesenchymal transition in thyroid carcinoma. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 36:218–222. 2014.(In Chinese). PubMed/NCBI | |
Janda E, Lehmann K, Killisch I, Jechlinger M, Herzig M, Downward J, Beug H and Grünert S: Ras and TGF[beta] cooperatively regulate epithelial cell plasticity and metastasis: Dissection of Ras signaling pathways. J Cell Biol. 156:299–313. 2002. View Article : Google Scholar : PubMed/NCBI | |
Vasko V, Espinosa AV, Scouten W, He H, Auer H, Liyanarachchi S, Larin A, Savchenko V, Francis GL, de la Chapelle A, et al: Gene expression and functional evidence of epithelial-to-mesenchymal transition in papillary thyroid carcinoma invasion. Proc Natl Acad Sci USA. 104:2803–2808. 2007. View Article : Google Scholar : PubMed/NCBI | |
Nakajima S, Doi R, Toyoda E, Tsuji S, Wada M, Koizumi M, Tulachan SS, Ito D, Kami K, Mori T, et al: N-cadherin expression and epithelial-mesenchymal transition in pancreatic carcinoma. Clin Cancer Res. 10:4125–4133. 2004. View Article : Google Scholar : PubMed/NCBI | |
Wada N, Duh QY, Sugino K, Iwasaki H, Kameyama K, Mimura T, Ito K, Takami H and Takanashi Y: Lymph node metastasis from 259 papillary thyroid microcarcinomas: Frequency, pattern of occurrence and recurrence, and optimal strategy for neck dissection. Ann Surg. 237:399–407. 2003. View Article : Google Scholar : PubMed/NCBI | |
Sakorafas GH, Giotakis J and Stafyla V: Papillary thyroid microcarcinoma: A surgical perspective. Cancer Treat Rev. 31:423–438. 2005. View Article : Google Scholar : PubMed/NCBI | |
White ML, Gauger PG and Doherty GM: Central lymph node dissection in differentiated thyroid cancer. World J Surg. 31:895–904. 2007. View Article : Google Scholar : PubMed/NCBI | |
Ito Y, Jikuzono T, Higashiyama T, Asahi S, Tomoda C, Takamura Y, Miya A, Kobayashi K, Matsuzuka F, Kuma K and Miyauchi A: Clinical significance of lymph node metastasis of thyroid papillary carcinoma located in one lobe. World J Surg. 30:1821–1828. 2006. View Article : Google Scholar : PubMed/NCBI | |
Lee YS, Kim SW, Kim SW, Kim SK, Kang HS, Lee ES and Chung KW: Extent of routine central lymph node dissection with small papillary thyroid carcinoma. World J Surg. 31:1954–1959. 2007. View Article : Google Scholar : PubMed/NCBI | |
Wang W, Gu J, Shang J and Wang K: Correlation analysis on central lymph node metastasis in 276 patients with cN0 papillary thyroid carcinoma. Int J Clin Exp Pathol. 6:510–515. 2013.PubMed/NCBI | |
Shin HJ, Kim EK, Moon HJ, Yoon JH, Han KH and Kwak JY: Can increased tumoral vascularity be a quantitative predicting factor of lymph node metastasis in papillary thyroid microcarcinoma? Endocrine. 47:273–282. 2014. View Article : Google Scholar : PubMed/NCBI | |
Park YJ, Kim YA, Lee YJ, Kim SH, Park SY, Kim KW, Chung JK, Youn YK, Kim KH, Park DJ and Cho BY: Papillary microcarcinoma in comparison with larger papillary thyroid carcinoma in BRAF(V600E) mutation, clinicopathological features, and immunohistochemical findings. Head Neck. 32:38–45. 2010.PubMed/NCBI |