J Endocr Surg.  2018 Sep;18(3):191-198. 10.16956/jes.2018.18.3.191.

Prediction of Contralateral Occult Malignant Nodule in Patients with Unilaterally Confined Papillary Thyroid Carcinomas

Affiliations
  • 1Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea. hasus@hanmail.net

Abstract

PURPOSE
The purpose of this study was to assess the presence of contralateral occult malignant foci (OMF) among patients who confined unilateral papillary thyroid carcinomas (PTCs).
METHODS
From January 2010 to December 2012, we retrospectively evaluated 714 patients who received total thyroidectomy with central lymph node (LN) dissection after being diagnosed as having unilaterally confined PTC. By dividing the patients into 2 groups according to the presence or absence of contralateral OMF, the relationship between OMF and clinicopathological factors such as age, sex, tumor size, multifocality, chronic lymphocytic/Hashimoto's thyroiditis, contralateral lobe benign nodule, extrathyroidal extension (ETE), and central LN metastasis.
RESULTS
When the patients were subdivided based on primary tumor size, OMF in the contralateral lobe were more frequently found as the tumor sizes increased, with statistical significance (P=0.012). In the patients with multifocal thyroid cancer in the lobe that had primary tumor, OMF was observed in the other lobe regardless of the number of primary malignant nodules, and the difference was statistically significant (P=0.001).
CONCLUSION
The primary tumor size or multifocality is a risk factor that can predict the presence of contralateral lobe occult cancers. We suggest that patient needs to carefully observe the remaining contralateral lobe, taking into consideration the size and multifocality of the primary tumor, when performing unilateral thyroid lobectomy.

Keyword

Papillary thyroid carcinoma; Contralateral occult malignant foci

MeSH Terms

Humans
Lymph Nodes
Neoplasm Metastasis
Retrospective Studies
Risk Factors
Thyroid Gland*
Thyroid Neoplasms*
Thyroidectomy
Thyroiditis

Reference

1. Kim EK, Park CS, Chung WY, Oh KK, Kim DI, Lee JT, et al. New sonographic criteria for recommending fine-needle aspiration biopsy of nonpalpable solid nodules of the thyroid. AJR Am J Roentgenol. 2002; 178:687–691.
Article
2. Hong YJ, Son EJ, Kim EK, Kwak JY, Hong SW, Chang HS. Positive predictive value of sonographic features of solid thyroid nodule. Clin Imaging. 2010; 34:127–133.
Article
3. Siegel R, Ma J, Zou A, Ahmedin J. Cancer statistics, 2014. CA Cancer J Clin. 2014; 64:9–29.
Article
4. Markovina S, Grigsby PW, Schwarz JK, DeWees T, Moley JF, Siegel BA, et al. Treatment approach, surveillance, and outcome of well-differentiated thyroid cancer in childhood and adolescence. Thyroid. 2014; 24:1121–1126.
Article
5. American Thyroid Association (ATA) Guidelines Taskforce on Thyroid Nodules and Differentiated Thyroid Cancer. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 2009; 19:1167–1214.
6. Pasieka JL, Thompson NW, McLeod MK, Burney RE, Macha M. The incidence of bilateral well-differentiated thyroid cancer found at completion thyroidectomy. World J Surg. 1992; 16:711–716.
Article
7. So YK, Kim MW, Son YI. Multifocality and bilaterality of papillary thyroid microcarcinoma. Clin Exp Otorhinolaryngol. 2015; 8:174–178.
Article
8. Yi KH, Park YJ, Koong SS, Kim JH, Na DG, Ryu JS, et al. Revised Korean Thyroid Association management guidelines for patients with thyroid nodules and thyroid cancer. Endocrinol Metab (Seoul). 2010; 25:270–297.
Article
9. Yi KH, Park YJ, Koong SS, Kim JH, Na DG, Ryu JS, et al. Revised Korean Thyroid Association management guidelines for patients with thyroid nodules and thyroid cancer. Korean J Otorhinolaryngol-Head Neck Surg. 2011; 54:8–36.
Article
10. Edge SB. American Joint Committee on Cancer. AJCC Cancer Staging Manual. 7th ed. New York (NY): Springer;2010.
11. Stojadinovic A, Peoples GE, Libutti SK, Henry LR, Eberhardt J, Howard RS, et al. Development of a clinical decision model for thyroid nodules. BMC Surg. 2009; 9:12.
Article
12. 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; 114:1050–1057.
13. Hay ID, Thompson GB, Grant CS, Bergstralh EJ, Dvorak CE, Gorman CA, et al. Papillary thyroid carcinoma managed at the Mayo Clinic during six decades (1940–1999): temporal trends in initial therapy and long-term outcome in 2444 consecutively treated patients. World J Surg. 2002; 26:879–885.
Article
14. Matsuzu K, Sugino K, Masudo K, Nagahama M, Kitagawa W, Shibuya H, et al. Thyroid lobectomy for papillary thyroid cancer: long-term follow-up study of 1,088 cases. World J Surg. 2014; 38:68–79.
Article
15. Nixon IJ, Ganly I, Patel SG, Palmer FL, Whitcher MM, Tuttle RM, et al. Thyroid lobectomy for treatment of well differentiated intrathyroid malignancy. Surgery. 2012; 151:571–579.
Article
16. Amin MB, Edge SB. American Joint Committee on Cancer. AJCC Cancer Staging Manual. 8th ed. Switzerland: Springer;2017.
17. Hendrickson-Rebizant J, Sigvaldason H, Nason RW, Pathak KA. Identifying the most appropriate age threshold for TNM stage grouping of well-differentiated thyroid cancer. Eur J Surg Oncol. 2015; 41:1028–1032.
Article
18. Ito Y, Fukushima M, Tomoda C, Inoue H, Kihara M, Higashiyama T, et al. Prognosis of patients with papillary thyroid carcinoma having clinically apparent metastasis to the lateral compartment. Endocr J. 2009; 56:759–766.
Article
19. Ito Y, Ichihara K, Masuoka H, Fukushima M, Inoue H, Kihara M, et al. Establishment of an intraoperative staging system (iStage) by improving UICC TNM classification system for papillary thyroid carcinoma. World J Surg. 2010; 34:2570–2580.
Article
20. Kim SJ, Myong JP, Suh H, Lee KE, Youn YK. Optimal cutoff age for predicting mortality associated with differentiated thyroid cancer. PLoS One. 2015; 10:e0130848.
Article
21. Mazurat A, Torroni A, Hendrickson-Rebizant J, Benning H, Nason RW, Pathak KA. The age factor in survival of a population cohort of well-differentiated thyroid cancer. Endocr Connect. 2013; 2:154–160.
Article
22. Kasai N, Sakamoto A. New subgrouping of small thyroid carcinomas. Cancer. 1987; 60:1767–1770.
Article
23. 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
24. Yi KH, Lee EK, Kang HC, Koh Y, Kim SW, Kim IJ, et al. 2016 revised Korean Thyroid Association management guidelines for patients with thyroid nodules and thyroid cancer. Int J Thyroidol. 2016; 9:59–126.
Article
25. Park JW, Chung KW, Yun JS, Kwon H, Kim HY, Nam KH, et al. Surgical treatment guidelines for patients with differentiated thyroid cancer: the Korean Association of Thyroid and Endocrine surgeons (KATES) Guidelines Taskforce. Korean J Endocr Surg. 2017; 17:1–18.
Article
26. Arora N, Turbendian HK, Scognamiglio T, Wagner PL, Goldsmith SJ, Zarnegar R, et al. Extrathyroidal extension is not all equal: implications of macroscopic versus microscopic extent in papillary thyroid carcinoma. Surgery. 2008; 144:942–947.
Article
27. Leboulleux S, Rubino C, Baudin E, Caillou B, Hartl DM, Bidart JM, et al. Prognostic factors for persistent or recurrent disease of papillary thyroid carcinoma with neck lymph node metastases and/or tumor extension beyond the thyroid capsule at initial diagnosis. J Clin Endocrinol Metab. 2005; 90:5723–5729.
Article
28. Radowsky JS, Howard RS, Burch HB, Stojadinovic A. Impact of degree of extrathyroidal extension of disease on papillary thyroid cancer outcome. Thyroid. 2014; 24:241–244.
Article
29. Shin JH, Ha TK, Park HK, Ahn MS, Kim KH, Bae KB, et al. Implication of minimal extrathyroidal extension as a prognostic factor in papillary thyroid carcinoma. Int J Surg. 2013; 11:944–947.
Article
30. Woo CG, Sung CO, Choi YM, Kim WG, Kim TY, Shong YK, et al. Clinicopathological significance of minimal extrathyroid extension in solitary papillary thyroid carcinomas. Ann Surg Oncol. 2015; 22:Suppl 3. S728–S733.
Article
31. Kim ES, Kim TY, Koh JM, Kim YI, Hong SJ, Kim WB, et al. Completion thyroidectomy in patients with thyroid cancer who initially underwent unilateral operation. Clin Endocrinol (Oxf). 2004; 61:145–148.
Article
32. Koo BS, Lim HS, Lim YC, Yoon YH, Kim YM, Park YH, et al. Occult contralateral carcinoma in patients with unilateral papillary thyroid microcarcinoma. Ann Surg Oncol. 2010; 17:1101–1105.
Article
33. Zhou YL, Zhang W, Gao EL, Dai XX, Yang H, Zhang XH, et al. Preoperative BRAF mutation is predictive of occult contralateral carcinoma in patients with unilateral papillary thyroid microcarcinoma. Asian Pac J Cancer Prev. 2012; 13:1267–1272.
Article
34. Park SY, Park YJ, Lee HS, Choi SH, Choe G, Jang HC, et al. Analysis of differential BRAF V600E mutational status in multifocal papillary thyroid carcinoma. Cancer. 2006; 107:1831–1838.
Article
35. Giannini R, Ugolini C, Lupi C, Proietti A, Elisei R, Salvatore G, et al. The heterogeneous distribution of BRAF mutation supports the independent clonal origin of distinct tumor foci in multifocal papillary thyroid carcinoma. J Clin Endocrinol Metab. 2007; 92:3511–3516.
Article
36. Sugg SL, Ezzat S, Rosen IB, Freeman JL, Asa SL. Distinct multiple RET/PTC gene rearrangement in multifocal papillary thyroid neoplasia. J Clin Endocrinol Metab. 1998; 83:4116–4122.
Article
37. Wang W, Zhao W, Wang H, Teng X, Wang H, Chen X, et al. Poorer prognosis and higher prevalence of BRAF (V600E) mutation in synchronous bilateral papillary thyroid carcinoma. Ann Surg Oncol. 2012; 19:31–36.
Article
38. Tuttle RM, Lemar H, Burch HB. Clinical features associated with an increased risk of thyroid malignancy in patients with follicular neoplasia by fine-needle aspiration. Thyroid. 1998; 8:377–383.
Article
39. Goldstein RE, Netterville JL, Burkey B, Johnson JE. Implications of follicular neoplasms, atypia, and lesions suspicious for malignancy diagnosed by fine-needle aspiration of thyroid nodules. Ann Surg. 2002; 235:656–662.
Article
40. Schlinkert RT, van Heerden JA, Goellner JR, Gharib H, Smith SL, Rosales RF, et al. Factors that predict malignant thyroid lesions when fine-needle aspiration is “suspicious for follicular neoplasm”. Mayo Clin Proc. 1997; 72:913–916.
Article
41. Mehta RS, Carty SE, Ohori NP, Hodak SP, Coyne C, LeBeau SO, et al. Nodule size is an independent predictor of malignancy in mutation-negative nodules with follicular lesion of undetermined significance cytology. Surgery. 2013; 154:730–736.
Article
42. Jeon MJ, Kim WG, Kwon HM, Kim MJ, Park SY, Oh SY, et al. Clinical outcomes after delayed thyroid surgery in patients with papillary thyroid microcarcinoma. Eur J Endocrinol. 2017; 177:25–31.
Article
43. Ito Y, Miyauchi A, Oda H. Low-risk papillary microcarcinoma of the thyroid: a review of active surveillance trials. Eur J Surg Oncol. 2018; 44:307–315.
Article
44. Pitt SC, Sippel RS, Chen H. Contralateral papillary thyroid cancer: does size matter? Am J Surg. 2009; 197:342–347.
Article
45. Lee YC, Eun YG, Sohn YM, Rhee SY, Hong IK, Chon S, et al. Predictive factors for occult contralateral carcinoma in patients with unilateral papillary thyroid microcarcinoma by preoperative ultrasonographic and pathological features. World J Surg. 2015; 39:1736–1741.
Article
46. Ito Y, Miyauchi A. Nonoperative management of low-risk differentiated thyroid carcinoma. Curr Opin Oncol. 2015; 27:15–20.
Article
Full Text Links
  • JES
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr