Acessibilidade / Reportar erro

Risk of malignancy and diagnostic accuracy of fine-needle aspiration biopsy in thyroid nodules with diameters greater than 4 centimeters

ABSTRACT

Objective:

The risk of malignancy and diagnostic accuracy of fine-needle aspiration biopsy (FNAB) of thyroid nodules (TN) with diameters ≥ 3-4 cm remains controversial. However, some groups have indicated surgical treatment in these patients regardless of the FNAB results. We aimed to evaluate the diagnostic accuracy of the FNAB in systematically resected ≥4 cm TN and if the risk of malignancy is higher in these patients.

Subjects and methods:

We retrospectively evaluated 138 patients (142 nodules) with TN with diameters ≥4 cm who underwent thyroidectomy.

Results:

The FNAB results were nondiagnostic/unsatisfactory (ND/UNS) in 2.1% of the cases and benign in 51.4%. They indicated atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS) in 23.9% of cases, follicular neoplasia/suspicious for a follicular neoplasm (FN/SFN) in 9.2%, suspicion of malignancy (SUS) in 8.5%, and malignant in 4.9%. The histopathological analysis after thyroidectomy revealed a thyroid cancer rate of 100% in the FNABs classified as malignant, 33.3% in SUS cases, 7.7% in FN/SFN, 17.6% in AUS/FLUS, and 4.1% in benign FNABs. None of the ND/UNS FNABs were malignant. The global malignancy diagnosis was 14.8% (n = 21). However, the rate of false negatives for FNAB was low (4.1%).

Conclusion:

We showed that the risk of malignancy in nodules with diameters ≥4 cm was higher compared to the risk of thyroid cancer in TN in general. However, we found a low rate of false-negative cytological results; therefore, our data do not justify the orientation of routine resection for these larger nodules.

Keywords
Thyroid nodule; fine-needle aspiration biopsy; thyroid ultrasound; diagnostic accuracy of fine-needle aspiration biopsy; risk of malignancy

INTRODUCTION

Thyroid nodules (TNs) are common clinical findings, with a prevalence of physical examination of approximately 5% in women and 1% in men, particularly in areas where iodine intake is normal (11 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., 22 Rosario PW, Ward LS, Carvalho GA, Graf H, Maciel RM, Maciel LM, et al. Sociedade Brasileira de Endocrinologia e Metabologia. Thyroid nodules and differentiated Thyroid cancer: update on the Brazilian consensus. Arq Bras Endocrinol Metabol. 2013;57:240-64.). However, the advent of thyroid ultrasound (US) has completely changed the panorama of thyroid nodule diagnosis. When used in routine examinations, this tool identifies thyroid nodules in 37-68% of the population, depending on gender and age (33 Campanella P, Ianni F, Rota CA, Corsello SM, Pontecorvi A. Quantification of cancer risk of each clinical and ultrasonographic suspicious feature of Thyroid nodules: a systematic review and meta-analysis. Eur J Endocrinol. 2014;170:R203-11.55 Lin JD, Chao TC, Huang BY, Chen ST, Chang HY, Hsueh C. Thyroid cancer in the Thyroid nodules evaluated by ultrasonography and fine-needle aspiration cytology. Thyroid. 2005;15:708-17.). As a result of this overdiagnosis, the incidence of thyroid cancer has tripled in the last three decades. This increase is almost entirely due to microcarcinomas (<1 cm in diameter), which have an excellent long-term prognosis (66 Janovsky CCPS, Bittencourt MS, Novais MAP, Maciel RMB, Biscolla RPM, Zucchi P. Thyroid cancer burden and economic impact on the Brazilian public health system. Arch Endocrinol Metab. 2018;62(5):537-44., 77 Lim H, Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in Thyroid Cancer Incidence and Mortality in the United States, 1974-2013. JAMA. 2017;317:1338-48.).

The main complementary exam in the investigation of a TN is fine-needle aspiration biopsy (FNAB) (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.). This test is indicated depending on the nodules’ size and characteristics as identified using US (11 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.). When performed by an experienced physician, FNAB provides reliable information; however, in some situations, the cytological study may be inconclusive, either because the material is insufficient or due to the lack of morphological diagnosis criteria (11 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.).

In recent years, less accurate FNAB has been described in nodules larger than 3-4 cm. Some researchers even claim that the FNAB, in these cases, is unreliable (99 Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.1616 Aydogan BI, Sahin M, Ceyhan K, Deniz O, Demir Ö, Emral R, et al. The influence of thyroid nodule size on the diagnostic efficacy and accuracy of ultrasound guided fine-needle aspiration cytology. Diagn Cytopathol. 2019;47:682-7.) and that the prevalence of malignancy in these larger nodules is higher than in smaller nodules (1717 Meko JB, Norton JA. Large cystic/solid Thyroid nodules: a potential false- negative fine-needle aspiration. Surgery. 1995;118:996-1003.1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.). This issue is significant because several researchers recommend the surgical removal of nodules with diameters ≥4 cm regardless of cytology results (99 Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.,1313 McCoy KL, Jabbour N, Ogilvie JB, Ohori NP, Carty SE, Yim JH. The incidence of cancer and rate of false-negative cytology in Thyroid nodules greater than or equal to 4 cm in size. Surgery. 2007;142:837-44; discussion 844.e1-3.,1717 Meko JB, Norton JA. Large cystic/solid Thyroid nodules: a potential false- negative fine-needle aspiration. Surgery. 1995;118:996-1003.,1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.,2020 Shin JJ, Caragacianu D, Randolph GW. Impact of Thyroid nodule size on prevalence and post-test probability of malignancy: A systematic review. Laryngoscope. 2015;125:263-72.). However, this issue remains controversial. Other studies have found no difference in the frequency of malignancy and the proportion of FNAB false-negative rates when comparing nodules larger than 4 cm in diameter with those that are smaller (2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10.3030 Megwalu UC. Risk of Malignancy in Thyroid Nodules 4 cm or Larger. Endocrinol Metab (Seoul). 2017;32:77-82.). Thus, this study aimed to evaluate the accuracy of cytology results obtained by FNAB in nodules with diameters ≥4 cm and whether the risk of malignancy is greater in these cases.

SUBJECTS AND METHODS

Patients

In this study, we retrospectively evaluated data from 666 thyroid nodules from 500 patients. Of these, we included 142 nodules with diameters greater than or equal to 4 cm (from 138 patients). All patients with a thyroid nodule ≥ 4 cm underwent thyroidectomy. Patients with hyperfunctioning nodules based on scintigraphy results, previous differentiated thyroid carcinoma (DTC), medullary thyroid carcinoma, familial non-medullary thyroid carcinoma (two or more first-degree relatives with DTC), previous thyroidectomy, suspicion of Gardner's syndrome, or incomplete medical records were excluded from the study. All patients attended the Center for Thyroid Diseases (Unifesp) and Instituto Israelita de Ensino e Pesquisa Albert Einstein from 2011 to 2014. This study was approved by Unifesp's ethics and research committee (CAAE: 36868514.7.0000.5505).

We recorded information such as age, sex, family history of thyroid disease, exposure to ionizing radiation, compressive symptoms, previous thyroid disease, and laboratory evaluation of thyroid function (TSH) for each patient. Information about the nodules’ size and characteristics was collected using US. All FNABs were guided by US, followed by cytological analysis of the aspirated material according to the Bethesda classification (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.). The same professionals performed all US and cytological analyses of the materials obtained from the FNAB. All thyroidectomies were performed by the same team of head and neck surgeons at the Center for Thyroid Diseases.

Thyroid ultrasound

US was performed using ATL model HDI 3500 equipment (Advanced Technologies Laboratories, USA) and a linear transducer with a frequency of 7.5-10 MHz. US characteristics analyzed included thyroid volume and morphology, number and volume of nodules, content, margin, echogenicity, halo, presence of calcifications, and vascularization on Doppler (3131 Kwak JY, Han KH, Yoon JH, Moon HJ, Son EJ, Park SH, et al. Thyroid imaging reporting and data system for US features of nodules: a step in establishing better stratification of cancer risk. Radiology. 2011;260:892-9.).

Fine needle aspiration biopsy and cytological analysis

FNAB was performed in single nodules ≥1 cm, regardless of the US characteristics, and in suspicious or dominant nodules if a multinodular goiter is present. For FNAB, 10 mL syringes were used coupled with 20 × 0.55 mm (24 G) needles. The material obtained via FNAB was fixed and stained using the Panoptic technique.

To define the sample as sufficient, we used the criteria suggested by the Guidelines of the Papanicolaou Society, which indicates that the sample must present at least six groups of follicular cells with at least ten cells per group with intact nuclei (3232 Guidelines of the Papanicolaou Society of Cytopathology for fine-needle aspiration procedure and reporting. The Papanicolaou Society of Cytopathology Task Force on Standards of Practice. Diagn Cytopathol. 1997;17:239-47.).

The cytological analysis of the aspirate was classified according to the Bethesda System for Reporting Thyroid Cytopathology: non-diagnostic/unsatisfactory (class I), benign (class II), atypia of undetermined meaning/follicular lesion of undetermined meaning (class III), neoplasia follicular/suspicious for follicular neoplasia (class IV), suspicious for malignancy (class V), or malignant (class VI) (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.).

Histopathological

FNAB results were considered false negatives when the nodules had benign cytological and malignant pathological diagnoses. False positives were considered cases whose cytological analyses were class III, class IV, class V or class VI according to the Bethesda System (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.) and the benign histopathological analysis.

The same pathological anatomy service performed the histopathological analysis of all cases at the Center for Thyroid Diseases. Given conflicting results (histology versus cytology), the review was performed by more than one professional in the group. We adopt pathological reports according to the 5th edition of the WHO Classification of Endocrine and Neuroendocrine Tumors (3333 Baloch ZW, Asa SL, Barletta JA, Ghossein RA, Juhlin CC, Jung CK, et al. Overview of the 2022 WHO Classification of Thyroid Neoplasms. Endocr Pathol. 2022;33(1):27-63.).

TSH measurement

TSH measurement was performed using a chemiluminescence method (Elecsys TSH, Roche Diagnostics, Mannheim, Germany; reference values: 0.35-5.5 mIU/L with detection limit 0.01 mIU/L).

Statistical analysis

Quantitative variables were assessed using Student's t-test (or Mann-Whitney test) and Spearman's correlation, as necessary. The proportions were compared using the Q-square test (or Fisher, when necessary). Comparisons between 3 or more groups were made using the Kruskal-Wallis test, with Dunn's post-test. Also, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were calculated according to the methodology used by Galen and Gambino (3434 Galen RS, Gambino SR. Beyond normality-the predictive value and efficiency of medical diagnosis. New York: Wiley; 1975.). For statistical analysis, we used the SPSS v21 software for Windows, and a significance was set at p < 0.05.

RESULTS

One hundred thirty-eight patients with 142 thyroid nodules ≥4 cm were operated on consecutively. Of these patients, 13 were men (9.4%), and 125 were women (90.6%). The median age was 46 years (ranging from 19-73 years). No patient reported exposure to ionizing radiation. Forty-four patients had compressive symptoms (31.9%). The median TSH value was 1.16 mIU/L (0.46-5.78 mIU/L). The median follow-up time for the group was eight months (ranging from 2-47 months).

Ultrasonographic characteristics and their ability to diagnose malignancy were obtained for all nodules evaluated and are shown in Table 1. In this analysis, we observed that microcalcification and partial or absent halo could distinguish malignant nodules from benign ones. When these two characteristics were evaluated in an associated way (presence of microcalcifications and missing or partial halo), we also observed a significant difference (p = 0.0001) with a relative risk of 6.8 (95% confidence interval, 2.09-22.11). Sensitivity was 85%, but specificity was 61.6%. The NPV was 95.8%, whereas the PPV was 28.3%.

Table 1
Ultrasound characteristics in thyroid nodules and their ability to differentiate between malignant and benign lesions

Partial thyroidectomy was the initial surgical approach in 63 of 138 patients (45.6%); however, three patients (2.2%) underwent a second operation for totalization. In the others (52.2%), the initial surgical approach was total thyroidectomy. Although all patients underwent surgery systematically for nodules greater than or equal to 4.0 cm, in 134 cases (97%), patients already had a formal surgical indication due to the suspected FNAB results, the presence of compressive symptoms, large goiters suspected, cytology in material obtained from FNAB from a nodule other than the most massive, or nodule growth.

Table 2 shows the frequency of malignancy in nodules ≥ 4 cm for each of Bethesda's cytological categories. Overall, most nodules showed a histopathological result of benignity, and the percentage of malignancy in nodules ≥ 4.0 cm was 14.8%.

Table 2
Frequency of malignancy in nodule ≥ 4 cm according to FNAB

Table 3 shows the clinical and histopathological characteristics of the cases studied. The female-to-male ratio was lower in the comparison of malignant and benign nodules. Also, patients with malignant nodules were younger and had a greater concomitance of Hashimoto's thyroiditis.

Table 3
Clinical and histopathological characteristics of the cases studied

The most common histological type was papillary carcinoma (78.3%), and classical and follicular variants were the most frequent (21.7% for both). Only 3 of 21 patients with carcinoma had benign cytological results. FNAB results were considered false positives when classes III-VI had benign histology (66 of 142). Thus, the cytology sensitivity was 87%, with a specificity of 60.3%, PPV of 30.3%, VPN of 95.9%, and accuracy of 64.4%. The false-negative cytology rate in nodules with diameters greater than or equal to 4 cm was 4.1% (p = 0.0005). Table 4 shows the clinical and histopathological characteristics of the 3 cases with false negative results.

Table 4
Characteristics of the three patients with false-negative cytology results

This study evaluated 65 of the 142 nodules (45.8%) as part of multinodular goiter (MNG). The rest of the patients had a single nodule. The percentage of malignancy in the index nodules among patients with MNG was 13.8% (9 of 65), whereas it was 18.2% (14 of 77) in those with unimodular goiter (p = 0.498).

DISCUSSION

FNAB of thyroid nodules is the main test to distinguish benign nodules from malignant ones (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.). It has good sensitivity and specificity and has contributed significantly to the reduction of unnecessary surgeries, especially with the introduction of the US to guide the procedure (3535 Hegedüs L. Clinical practice. The Thyroid nodule. N Engl J Med. 2004;351:1764-71.3737 Jing X, Michael CW, Pu RT. The clinical and diagnostic impact of using standard criteria of adequacy assessment and diagnostic terminology on Thyroid nodule fine needle aspiration. Diagn Cytopathol. 2008;36:161-6.). Although FNAB is an excellent diagnostic tool for TNs, some researchers believe the procedure has limitations, as it presents a high rate of false negatives, especially in nodules with diameters ≥ 3-4 cm (3838 Ucar AE, Sarikaya SM, Parlak Ö, Yalçin A. Effect of nodule size on the reliability of fine-needle aspiration biopsy in Thyroid nodules. Turk J Med Sci. 2014;44:1002-9., 3939 Raguin T, Schneegans O, Rodier JF, Volkmar PP, Sauleau E, Debry C, et al. Value of fine-needle aspiration in evaluating large Thyroid nodules. Head Neck. 2017;39:32-6.). This subject has been widely discussed in the literature, but no consensus has been reached (4040 Jinih M, Faisal F, Abdalla K, Majeed M, A Achakzai A, Heffron C, McCarthy J, Redmond JP. Association Between Thyroid Nodule Size and Malignancy Rate. Ann R Coll Surg Engl. 2020;102:43-8.).

In the present study, we showed that the FNAB false-negative rate in TNs with diameters ≥ 4 cm was relatively low (4.1%). Many studies have reported false-negative rates as low as 0-4% (2222 Al Dawish MA, Robert AA, Thabet MA, Braham R. Thyroid Nodule Management: Thyroid-Stimulating Hormone, Ultrasound, and Cytological Classification System for Predicting Malignancy. Cancer Informatics. 2018;17:1-9.,2525 Cavallo A, Johnson DN, White MG, Siddiqui S, Antic T, Mathew M, et al. Thyroid Nodule Size at Ultrasound as a Predictor of Malignancy and Final Pathologic Size. Thyroid. 2017; 27:641-50.,2727 Porterfield JR, Grant CS, Dean DS, Thompson GB, Farley DR, Richards ML. Reliability of benign fine needle aspiration cytology of large Thyroid nodules. Surgery. 2008;144:963-9.,2828 Raj MD, Grodski S, Woodruff S, Yeung M, Paul E, Serpell JW. Diagnostic lobectomy is not routinely required to exclude malignancy in thyroid nodules greater than four centimetres. ANZ J Surg. 2012;82:73-7.,3030 Megwalu UC. Risk of Malignancy in Thyroid Nodules 4 cm or Larger. Endocrinol Metab (Seoul). 2017;32:77-82.,4141 Nam SJ, Kwak JY, Moon HJ, Yoon JH, Kim EK, Koo JS. Large (≥3cm) thyroid nodules with benign cytology: Can Thyroid Imaging Reporting and Data System 9TIRADS) help predict false-negative cytology? PLoS One. 2017;12(10):e0186242.). However, for other researchers, the percentages have been as high as 10%-30% (Table 5) (9-16,21). One reason for this disagreement may be how patients are selected for surgery in various studies. Many studies in this area are retrospective, and not all patients with TNs with diameters ≥ 3-4 cm were referred for thyroidectomy. In some studies, only TNs with some characteristics of greater suspicion, such as cytological findings and suspicious US characteristics, nodule growth, and compressive symptoms, were submitted to surgery (1414 Koo DH, Song K, Kwon H, Bae DS, Kim JH, Min HS, et al. Does Tumor Size Influence the Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Cytology for Thyroid Nodules? Int J Endocrinol. 2016;2016:3803647.,1616 Aydogan BI, Sahin M, Ceyhan K, Deniz O, Demir Ö, Emral R, et al. The influence of thyroid nodule size on the diagnostic efficacy and accuracy of ultrasound guided fine-needle aspiration cytology. Diagn Cytopathol. 2019;47:682-7.,2222 Al Dawish MA, Robert AA, Thabet MA, Braham R. Thyroid Nodule Management: Thyroid-Stimulating Hormone, Ultrasound, and Cytological Classification System for Predicting Malignancy. Cancer Informatics. 2018;17:1-9.,2424 Kuru B, Gulcelik NE, Gulcelik MA, Dincer H. The false negative rate of fine-needle aspiration cytology for diagnosing thyroid carcinoma in thyroid nodules. Langenbecks Arch Surg. 2010;395:127-32.). This could justify the increase in the percentage of false negatives. Other factors potentially involved in these disagreements include the experience of the cytopathologist (4242 Agcaoglu O, Aksakal N, Ozcinar B, Sarici IS, Ercan G, Kucukyilmaz M, et al. Factors That Affect the False-Negative Outcomes of Fine-Needle Aspiration Biopsy in Thyroid Nodules. Int J Endocrinol. 2013;2013:126084.), sampling errors in which the aspirated material did not refer to the index nodule (2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10., 4343 Bozbiyik O, Öztürk S, Ünver M, Erol V, Bayol Ü, Aydın C. Reliability of fine needle aspiration biopsy in large thyroid nodules. Turk J Surg. 2017;33:10-3.), tiny neoplastic foci within a very large nodule (2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10.), and the characteristics of TNs with large cystic components (4444 Braga M, Cavalcanti TC, Collaço LM, Graf H. Efficacy of ultrasound-guided fine-needle aspiration biopsy in the diagnosis of complex thyroid nodules. J Clin Endocrinol Metab. 2001;86:4089-91.). In fact, in the present study, 2 of 3 cases of carcinoma that had benign FNAB results had a cystic component at the US. A similar finding was described by Meko and Norton, who found a 17% false-negative rate in nodules ≥3 cm, which increased to about 30% when the TNs were mixed (3131 Kwak JY, Han KH, Yoon JH, Moon HJ, Son EJ, Park SH, et al. Thyroid imaging reporting and data system for US features of nodules: a step in establishing better stratification of cancer risk. Radiology. 2011;260:892-9.).

Table 5
Published literature evaluating false-negative rates in large thyroid nodules with histology

Another controversial aspect of the literature is whether TN size correlates with the malignancy rate. Several studies (99 Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.,1212 Kim JH, Kim NK, Oh YL, Kim HJ, Kim SY, Chung JH, et al. The Validity of Ultrasonography-Guided Fine Needle Aspiration Biopsy in Thyroid Nodules 4 cm or Larger Depends on Ultrasonography Characteristics. Endocrinol Metab (Seoul). 2014;29:545-52.,1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.,2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10.,2323 Rosario PW, Salles DS, Bessa B, Purisch S. Low false negative rate of cytology in thyroid nodules > or = 4 cm. Arq Bras Endocrinol Metabol. 2009;53:1143-5.2626 Magister MJ, Chaikhoutdinov I, Schaefer E, Williams N, Saunders B. Association of Thyroid Nodule Size and Bethesda Class with Rate of Malignant Disease. JAMA Otolaryngol Head Neck Surg. 2015;141:1089-95.) have shown that nodules ≥ 3-4 cm in diameter have a higher malignancy rate (12.7%-58.6%) compared to the average percentage of nodule malignancy in general (5%-10%) (11 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., 22 Rosario PW, Ward LS, Carvalho GA, Graf H, Maciel RM, Maciel LM, et al. Sociedade Brasileira de Endocrinologia e Metabologia. Thyroid nodules and differentiated Thyroid cancer: update on the Brazilian consensus. Arq Bras Endocrinol Metabol. 2013;57:240-64.). Some authors, inclusive, have indicated lobectomies for all TNs with diameters ≥ 3-4 cm, regardless of FNAB results (99 Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.,1313 McCoy KL, Jabbour N, Ogilvie JB, Ohori NP, Carty SE, Yim JH. The incidence of cancer and rate of false-negative cytology in Thyroid nodules greater than or equal to 4 cm in size. Surgery. 2007;142:837-44; discussion 844.e1-3.,1717 Meko JB, Norton JA. Large cystic/solid Thyroid nodules: a potential false- negative fine-needle aspiration. Surgery. 1995;118:996-1003.,1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.,2020 Shin JJ, Caragacianu D, Randolph GW. Impact of Thyroid nodule size on prevalence and post-test probability of malignancy: A systematic review. Laryngoscope. 2015;125:263-72.). Here, we showed that the overall malignancy rate was 14.8%, which is similar to the average described in the studies mentioned above (Table 6). However, Nam and cols. (4141 Nam SJ, Kwak JY, Moon HJ, Yoon JH, Kim EK, Koo JS. Large (≥3cm) thyroid nodules with benign cytology: Can Thyroid Imaging Reporting and Data System 9TIRADS) help predict false-negative cytology? PLoS One. 2017;12(10):e0186242.) found a low malignancy rate (3.6%) in a large series of nodules with diameters ≥3 cm. Similar data have been shown by Sutton and cols. In that study, increasing nodule size > 4 cm and high-risk ultrasound features were not associated with risk of malignancy. Also, authors found that patient age ≥55 years old was independently associated with significantly lower risk of malignancy (4545 Sutton W, Canner JK, Rooper LM, Prescott JD, Zeiger MA, Mathur A. Is patient age associated with risk of malignancy in a ≥4 cm cytologically benign thyroid nodule? Am J Surg. 2021;221(1):111-6.). In addition, Jinih and cols. recently assessed the malignancy rate in thyroid nodules stratified by size (1.0-1.9; 2.0-2.9; 3.0-3.9; 4.0-4.9, and > 5.0 cm). Although the malignancy rate was relatively high (17.6-21.9), it did not differ among the stratification ranges by size (4040 Jinih M, Faisal F, Abdalla K, Majeed M, A Achakzai A, Heffron C, McCarthy J, Redmond JP. Association Between Thyroid Nodule Size and Malignancy Rate. Ann R Coll Surg Engl. 2020;102:43-8.). On the other hand, Cipriani and cols. showed that, in all nodules ≥ 3 cm (13.1%) and ≥ 4 cm (20.9%), the risk of malignancy was lower than those < 3 cm (19.6%) and < 4 cm (19.9%) (4646 Cipriani NA, White MG, Angelos P, Grogan RH. Large Cytologically Benign Thyroid Nodules do Not Have High Rates of Malignancy or False-Negative Rates and Clinical Observation Should be Considered: A Meta-Analysis. Thyroid. 2018;28(12):1595-608.).

Table 6
Published literature evaluating malignancy rate in large thyroid nodules with histology

Some authors have suggested that the nodules’ US characteristics are more important than their size and are decisive in defining the risk of malignancy (2727 Porterfield JR, Grant CS, Dean DS, Thompson GB, Farley DR, Richards ML. Reliability of benign fine needle aspiration cytology of large Thyroid nodules. Surgery. 2008;144:963-9.,4747 Yoon JH, Kwak JY, Moon HJ, Kim MJ, Kim EK. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy and the Sonographic Differences Between Benign and Malignant Thyroid Nodules 3 cm or Larger. Thyroid. 2011;21:993-1000.,4848 Peccin S, de Castro JA, Furlanetto TW, Furtado AP, Brasil BA, Czepielewski MA. Ultrasonography: Is it useful in the diagnosis of cancer in Thyroid nodules? J Endocrinol Invest. 2002;25:39-43.). Thus, in a large series of TNs with diameters ≥ 3 cm, Yoon and cols. (4747 Yoon JH, Kwak JY, Moon HJ, Kim MJ, Kim EK. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy and the Sonographic Differences Between Benign and Malignant Thyroid Nodules 3 cm or Larger. Thyroid. 2011;21:993-1000.) showed that the rate of false negatives in benign FNAB was low (1.8%). However, US characteristics suggestive of malignancy were more prevalent in FNABs that were malignant or suspected of malignancy than in cytology considered benign (70.3% vs. 1.2%). More recently, Hong and cols. also showed that, in a series of 2000 FNABs, the risk of malignancy did not increase as the nodules increased in size. However, patients with TNs with diameters ≥ 3.0 cm had a higher malignancy rate than those with TNs with diameters < 3.0 cm when US characteristics were of intermediate or low risk (1818 Hong MJ, Na DG, Baek JH, Sung JY, Kim JH. Impact of Nodule Size on Malignancy Risk Differs according to the Ultrasonography Pattern of Thyroid Nodules. Korean J Radiol. 2018;19:534-41.). In the present study, we showed that two US characteristics suggestive of malignancy (microcalcifications and partial or absent halo) could differentiate between malignant and benign TNs with high sensitivity (85%) and negative predictive value (95.8%). This demonstrates the importance of US findings in deciding whether or not to conduct surgery, even if the FNAB is benign.

The prevalence of each Bethesda diagnostic category varies widely in the literature. Class I, II, III, IV, V and VI findings represent 2%-20%, 57%-70%, 3%-8.2%, 2%-25%, 1%-6%, and 3%-14.4%, respectively (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.,1616 Aydogan BI, Sahin M, Ceyhan K, Deniz O, Demir Ö, Emral R, et al. The influence of thyroid nodule size on the diagnostic efficacy and accuracy of ultrasound guided fine-needle aspiration cytology. Diagn Cytopathol. 2019;47:682-7.,4949 Reuters KB, Mamone MC, Ikejiri ES, Camacho CP, Nakabashi CC, Janovsky CC, et al. Bethesda Classification and Cytohistological Correlation of Thyroid Nodules in a Brazilian Thyroid Disease Center. Eur Thyroid J. 2018;7:133-8.). The prevalence of each diagnostic category in the present study was 2.1%, 51.4%, 23.9, 9.2, 8.4, and 4.9 for classes I-VI, respectively. In the present series, the prevalence of FNAB in Bethesda category III was higher than that previously described for nodules of all sizes; however, they were similar to those described in studies that evaluated nodules with diameters ≥ 3-4 cm (99 Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.,1010 Mehanna R, Murphy M, McCarthy J, O’Leary G, Tuthill A, Murphy MS, et al. False negatives in thyroid cytology: impact of large nodule size and follicular variant of papillary carcinoma. Laryngoscope. 2013;123:1305-9.,1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.,5050 Ucler R, Usluogulları CA, Tam AA, Ozdemir D, Balkan F, Yalcın S, et al. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy for Thyroid Nodules Three Centimeters or Larger in Size. Diagn Cytopathol. 2015;43:622-8.). The risk of malignancy was 0%, 4.1%, 17.6%, 7.7%, 33.3%, and 100% for classes I, II, III, IV, V, and VI, respectively. Such findings are similar to those described in the literature, except for non-diagnosed FNABs, which, in several studies, show malignancy rates ranging from 5.3%-54% (88 Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.,1414 Koo DH, Song K, Kwon H, Bae DS, Kim JH, Min HS, et al. Does Tumor Size Influence the Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Cytology for Thyroid Nodules? Int J Endocrinol. 2016;2016:3803647.,1616 Aydogan BI, Sahin M, Ceyhan K, Deniz O, Demir Ö, Emral R, et al. The influence of thyroid nodule size on the diagnostic efficacy and accuracy of ultrasound guided fine-needle aspiration cytology. Diagn Cytopathol. 2019;47:682-7.,1919 Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.,2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10., 2323 Rosario PW, Salles DS, Bessa B, Purisch S. Low false negative rate of cytology in thyroid nodules > or = 4 cm. Arq Bras Endocrinol Metabol. 2009;53:1143-5.,2424 Kuru B, Gulcelik NE, Gulcelik MA, Dincer H. The false negative rate of fine-needle aspiration cytology for diagnosing thyroid carcinoma in thyroid nodules. Langenbecks Arch Surg. 2010;395:127-32.,2828 Raj MD, Grodski S, Woodruff S, Yeung M, Paul E, Serpell JW. Diagnostic lobectomy is not routinely required to exclude malignancy in thyroid nodules greater than four centimetres. ANZ J Surg. 2012;82:73-7.,4747 Yoon JH, Kwak JY, Moon HJ, Kim MJ, Kim EK. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy and the Sonographic Differences Between Benign and Malignant Thyroid Nodules 3 cm or Larger. Thyroid. 2011;21:993-1000.,4848 Peccin S, de Castro JA, Furlanetto TW, Furtado AP, Brasil BA, Czepielewski MA. Ultrasonography: Is it useful in the diagnosis of cancer in Thyroid nodules? J Endocrinol Invest. 2002;25:39-43.,5151 Aschebrook-Kilfoy B, Ward MH, Sabra MM, Devesa SS. Thyroid cancer incidence patterns in the United States by histologic type, 1992-2006. Thyroid. 2011;21:125-34.). Perhaps our study's small number of nodules with non-diagnostic cytology explains this disagreement, given that for classes III-VI, positive, sensitivity (87%), specificity (60.3%), PPV (30.3%), NPV (95.9%), and accuracy of cytology (64.4%) were comparable to previous studies (1414 Koo DH, Song K, Kwon H, Bae DS, Kim JH, Min HS, et al. Does Tumor Size Influence the Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Cytology for Thyroid Nodules? Int J Endocrinol. 2016;2016:3803647.,2929 Shrestha M, Crothers BA, Burch HB. The impact of thyroid nodule size on the risk of malignancy and accuracy of fineneedle aspiration: a 10-year study from a single institution. Thyroid. 2012;22:1251-6.,4747 Yoon JH, Kwak JY, Moon HJ, Kim MJ, Kim EK. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy and the Sonographic Differences Between Benign and Malignant Thyroid Nodules 3 cm or Larger. Thyroid. 2011;21:993-1000.).

The histological type of thyroid carcinoma most commonly found in TNs is papillary (85%), followed by follicular carcinoma (12%) and, more rarely, poorly differentiated thyroid carcinomas (<3%) (11 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.). In our study of nodules with diameters ≥ 4 cm, we found a lower percentage of papillary carcinoma (78.3%) than that described for thyroid carcinomas in general. In contrast, the rate of follicular carcinomas was relatively higher (3% of 21%, 14.3%), which is in line with previous studies (1111 Giles WH, Maclellan RA, Gawande AA, Ruan DT, Alexander EK, Moore FD Jr, et al. False Negative Cytology in Large Thyroid Nodules. Ann Surg Oncol. 2015;22:152-7.,1818 Hong MJ, Na DG, Baek JH, Sung JY, Kim JH. Impact of Nodule Size on Malignancy Risk Differs according to the Ultrasonography Pattern of Thyroid Nodules. Korean J Radiol. 2018;19:534-41.,2121 Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10.). Hashimoto's thyroiditis was found more frequently in patients with thyroid carcinomas than in patients with benign pathology. This phenomenon is well described in the literature (5252 Spencer C, LoPresti J, Fatemi S. How sensitive (second-generation) thyroglobulin measurement is changing paradigms for monitoring patients with differentiated thyroid cancer, in the absence or presence of thyroglobulin autoantibodies. Curr Opin Endocrinol Diabetes Obes. 2014;21:394-404.), and hypotheses such as the greater antigenicity of tumor thyroglobulin may justify this finding (5353 Xavier AC, Maciel RM, Vieira JG, Dias-da-Silva MR, Martins JR. Insights into the posttranslational structural heterogeneity of thyroglobulin and its role in the development, diagnosis, and management of benign and malignant thyroid diseases. Arch Endocrinol Metab. 2016;60:66-75.).

The strength of the present study was that the US, FNAB, and surgery were performed by the same group of qualified professionals dedicated to evaluating, diagnosing, and monitoring differentiated thyroid carcinomas. In addition, all patients with TNs with diameters greater than 4 cm underwent thyroidectomy. The weakness of the present study is that it is retrospective and does not evaluate false-negative rates for TNs with diameters less than 4 cm, making it impossible to know whether this rate would be lower in this subgroup of patients.

Finally, in the present study, we show that, although the malignancy rate in TNs with diameters ≥ 4 cm in diameter is high, the rate of benign FNAB false negatives in these same nodules is not high and does not justify the lobectomy or thyroidectomy procedure under such conditions. Further prospective studies with a higher number of cases are necessary to clarify this issue.

Acknowledgements

the authors thank the team from the Thyroid Disease Outpatient Clinic (Flávia F. Valente, Carolina C. P. Janovsky and Leonardo M. Tucci), and from the Laboratory of Molecular and Translational Endocrinology (Teresa S. Kasamatsu, Ilda S. Kunii). We also thank Ângela Maria Faria and Yeda Queiroga for her administrative assistance and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (Capes) – Finance Code 001, National Council for Scientific and Technological Development (CNPq) and São Paulo Research Foundation (Fundação de Amparo à Pesquisa do Estado de São Paulo – Fapesp) for Financial support.

REFERENCES

  • 1
    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.
  • 2
    Rosario PW, Ward LS, Carvalho GA, Graf H, Maciel RM, Maciel LM, et al. Sociedade Brasileira de Endocrinologia e Metabologia. Thyroid nodules and differentiated Thyroid cancer: update on the Brazilian consensus. Arq Bras Endocrinol Metabol. 2013;57:240-64.
  • 3
    Campanella P, Ianni F, Rota CA, Corsello SM, Pontecorvi A. Quantification of cancer risk of each clinical and ultrasonographic suspicious feature of Thyroid nodules: a systematic review and meta-analysis. Eur J Endocrinol. 2014;170:R203-11.
  • 4
    Durante C, Grani G, Lamartina L, Filetti S, Mandel SJ, Cooper DS. The diagnosis and management of thyroid nodules: A Review. JAMA. 2018;319:914-24.
  • 5
    Lin JD, Chao TC, Huang BY, Chen ST, Chang HY, Hsueh C. Thyroid cancer in the Thyroid nodules evaluated by ultrasonography and fine-needle aspiration cytology. Thyroid. 2005;15:708-17.
  • 6
    Janovsky CCPS, Bittencourt MS, Novais MAP, Maciel RMB, Biscolla RPM, Zucchi P. Thyroid cancer burden and economic impact on the Brazilian public health system. Arch Endocrinol Metab. 2018;62(5):537-44.
  • 7
    Lim H, Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in Thyroid Cancer Incidence and Mortality in the United States, 1974-2013. JAMA. 2017;317:1338-48.
  • 8
    Cibas ES, Ali SZ. The 2017 Bethesda System for Reporting Thyroid Cytopathology. Thyroid. 2017;27(11):1341-6.
  • 9
    Wharry LI, McCoy KL, Stang MT, Armstrong MJ, LeBeau SO, Tublin ME, et al. Thyroid nodules (≥4 cm): can ultrasound and cytology reliably exclude cancer? World J Surg. 2014;38:614-21.
  • 10
    Mehanna R, Murphy M, McCarthy J, O’Leary G, Tuthill A, Murphy MS, et al. False negatives in thyroid cytology: impact of large nodule size and follicular variant of papillary carcinoma. Laryngoscope. 2013;123:1305-9.
  • 11
    Giles WH, Maclellan RA, Gawande AA, Ruan DT, Alexander EK, Moore FD Jr, et al. False Negative Cytology in Large Thyroid Nodules. Ann Surg Oncol. 2015;22:152-7.
  • 12
    Kim JH, Kim NK, Oh YL, Kim HJ, Kim SY, Chung JH, et al. The Validity of Ultrasonography-Guided Fine Needle Aspiration Biopsy in Thyroid Nodules 4 cm or Larger Depends on Ultrasonography Characteristics. Endocrinol Metab (Seoul). 2014;29:545-52.
  • 13
    McCoy KL, Jabbour N, Ogilvie JB, Ohori NP, Carty SE, Yim JH. The incidence of cancer and rate of false-negative cytology in Thyroid nodules greater than or equal to 4 cm in size. Surgery. 2007;142:837-44; discussion 844.e1-3.
  • 14
    Koo DH, Song K, Kwon H, Bae DS, Kim JH, Min HS, et al. Does Tumor Size Influence the Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Cytology for Thyroid Nodules? Int J Endocrinol. 2016;2016:3803647.
  • 15
    Carrillo JF, Frias-Mendivil M, Ochoa-Carrillo FJ, Ibarra M. Accuracy of fine-needle aspiration biopsy of the Thyroid combined with an evaluation of clinical and radiologic factors. Otolaryngol Head Neck Surg. 2000;122:917-21.
  • 16
    Aydogan BI, Sahin M, Ceyhan K, Deniz O, Demir Ö, Emral R, et al. The influence of thyroid nodule size on the diagnostic efficacy and accuracy of ultrasound guided fine-needle aspiration cytology. Diagn Cytopathol. 2019;47:682-7.
  • 17
    Meko JB, Norton JA. Large cystic/solid Thyroid nodules: a potential false- negative fine-needle aspiration. Surgery. 1995;118:996-1003.
  • 18
    Hong MJ, Na DG, Baek JH, Sung JY, Kim JH. Impact of Nodule Size on Malignancy Risk Differs according to the Ultrasonography Pattern of Thyroid Nodules. Korean J Radiol. 2018;19:534-41.
  • 19
    Pinchot SN, Al-Wagih H, Schaefer S, Sippel R, Chen H. Accuracy of fine-needle aspiration biopsy for predicting neoplasm or carcinoma in thyroid nodules 4 cm or larger. Arch Surg. 2009;144:649-55.
  • 20
    Shin JJ, Caragacianu D, Randolph GW. Impact of Thyroid nodule size on prevalence and post-test probability of malignancy: A systematic review. Laryngoscope. 2015;125:263-72.
  • 21
    Albuja-Cruz MB, Goldfarb M, Gondek SS, Allan BJ, Lew JI. Reliability of fine-needle aspiration for thyroid nodules greater than or equal to 4 cm. J Surg Res. 2013;181:6-10.
  • 22
    Al Dawish MA, Robert AA, Thabet MA, Braham R. Thyroid Nodule Management: Thyroid-Stimulating Hormone, Ultrasound, and Cytological Classification System for Predicting Malignancy. Cancer Informatics. 2018;17:1-9.
  • 23
    Rosario PW, Salles DS, Bessa B, Purisch S. Low false negative rate of cytology in thyroid nodules > or = 4 cm. Arq Bras Endocrinol Metabol. 2009;53:1143-5.
  • 24
    Kuru B, Gulcelik NE, Gulcelik MA, Dincer H. The false negative rate of fine-needle aspiration cytology for diagnosing thyroid carcinoma in thyroid nodules. Langenbecks Arch Surg. 2010;395:127-32.
  • 25
    Cavallo A, Johnson DN, White MG, Siddiqui S, Antic T, Mathew M, et al. Thyroid Nodule Size at Ultrasound as a Predictor of Malignancy and Final Pathologic Size. Thyroid. 2017; 27:641-50.
  • 26
    Magister MJ, Chaikhoutdinov I, Schaefer E, Williams N, Saunders B. Association of Thyroid Nodule Size and Bethesda Class with Rate of Malignant Disease. JAMA Otolaryngol Head Neck Surg. 2015;141:1089-95.
  • 27
    Porterfield JR, Grant CS, Dean DS, Thompson GB, Farley DR, Richards ML. Reliability of benign fine needle aspiration cytology of large Thyroid nodules. Surgery. 2008;144:963-9.
  • 28
    Raj MD, Grodski S, Woodruff S, Yeung M, Paul E, Serpell JW. Diagnostic lobectomy is not routinely required to exclude malignancy in thyroid nodules greater than four centimetres. ANZ J Surg. 2012;82:73-7.
  • 29
    Shrestha M, Crothers BA, Burch HB. The impact of thyroid nodule size on the risk of malignancy and accuracy of fineneedle aspiration: a 10-year study from a single institution. Thyroid. 2012;22:1251-6.
  • 30
    Megwalu UC. Risk of Malignancy in Thyroid Nodules 4 cm or Larger. Endocrinol Metab (Seoul). 2017;32:77-82.
  • 31
    Kwak JY, Han KH, Yoon JH, Moon HJ, Son EJ, Park SH, et al. Thyroid imaging reporting and data system for US features of nodules: a step in establishing better stratification of cancer risk. Radiology. 2011;260:892-9.
  • 32
    Guidelines of the Papanicolaou Society of Cytopathology for fine-needle aspiration procedure and reporting. The Papanicolaou Society of Cytopathology Task Force on Standards of Practice. Diagn Cytopathol. 1997;17:239-47.
  • 33
    Baloch ZW, Asa SL, Barletta JA, Ghossein RA, Juhlin CC, Jung CK, et al. Overview of the 2022 WHO Classification of Thyroid Neoplasms. Endocr Pathol. 2022;33(1):27-63.
  • 34
    Galen RS, Gambino SR. Beyond normality-the predictive value and efficiency of medical diagnosis. New York: Wiley; 1975.
  • 35
    Hegedüs L. Clinical practice. The Thyroid nodule. N Engl J Med. 2004;351:1764-71.
  • 36
    Lew JI, Rodgers SE, Solorzano CC. Developments in the use of ultrasound for Thyroid cancer. Curr Opin Oncol. 2010;22:11-6.
  • 37
    Jing X, Michael CW, Pu RT. The clinical and diagnostic impact of using standard criteria of adequacy assessment and diagnostic terminology on Thyroid nodule fine needle aspiration. Diagn Cytopathol. 2008;36:161-6.
  • 38
    Ucar AE, Sarikaya SM, Parlak Ö, Yalçin A. Effect of nodule size on the reliability of fine-needle aspiration biopsy in Thyroid nodules. Turk J Med Sci. 2014;44:1002-9.
  • 39
    Raguin T, Schneegans O, Rodier JF, Volkmar PP, Sauleau E, Debry C, et al. Value of fine-needle aspiration in evaluating large Thyroid nodules. Head Neck. 2017;39:32-6.
  • 40
    Jinih M, Faisal F, Abdalla K, Majeed M, A Achakzai A, Heffron C, McCarthy J, Redmond JP. Association Between Thyroid Nodule Size and Malignancy Rate. Ann R Coll Surg Engl. 2020;102:43-8.
  • 41
    Nam SJ, Kwak JY, Moon HJ, Yoon JH, Kim EK, Koo JS. Large (≥3cm) thyroid nodules with benign cytology: Can Thyroid Imaging Reporting and Data System 9TIRADS) help predict false-negative cytology? PLoS One. 2017;12(10):e0186242.
  • 42
    Agcaoglu O, Aksakal N, Ozcinar B, Sarici IS, Ercan G, Kucukyilmaz M, et al. Factors That Affect the False-Negative Outcomes of Fine-Needle Aspiration Biopsy in Thyroid Nodules. Int J Endocrinol. 2013;2013:126084.
  • 43
    Bozbiyik O, Öztürk S, Ünver M, Erol V, Bayol Ü, Aydın C. Reliability of fine needle aspiration biopsy in large thyroid nodules. Turk J Surg. 2017;33:10-3.
  • 44
    Braga M, Cavalcanti TC, Collaço LM, Graf H. Efficacy of ultrasound-guided fine-needle aspiration biopsy in the diagnosis of complex thyroid nodules. J Clin Endocrinol Metab. 2001;86:4089-91.
  • 45
    Sutton W, Canner JK, Rooper LM, Prescott JD, Zeiger MA, Mathur A. Is patient age associated with risk of malignancy in a ≥4 cm cytologically benign thyroid nodule? Am J Surg. 2021;221(1):111-6.
  • 46
    Cipriani NA, White MG, Angelos P, Grogan RH. Large Cytologically Benign Thyroid Nodules do Not Have High Rates of Malignancy or False-Negative Rates and Clinical Observation Should be Considered: A Meta-Analysis. Thyroid. 2018;28(12):1595-608.
  • 47
    Yoon JH, Kwak JY, Moon HJ, Kim MJ, Kim EK. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy and the Sonographic Differences Between Benign and Malignant Thyroid Nodules 3 cm or Larger. Thyroid. 2011;21:993-1000.
  • 48
    Peccin S, de Castro JA, Furlanetto TW, Furtado AP, Brasil BA, Czepielewski MA. Ultrasonography: Is it useful in the diagnosis of cancer in Thyroid nodules? J Endocrinol Invest. 2002;25:39-43.
  • 49
    Reuters KB, Mamone MC, Ikejiri ES, Camacho CP, Nakabashi CC, Janovsky CC, et al. Bethesda Classification and Cytohistological Correlation of Thyroid Nodules in a Brazilian Thyroid Disease Center. Eur Thyroid J. 2018;7:133-8.
  • 50
    Ucler R, Usluogulları CA, Tam AA, Ozdemir D, Balkan F, Yalcın S, et al. The Diagnostic Accuracy of Ultrasound-Guided Fine-Needle Aspiration Biopsy for Thyroid Nodules Three Centimeters or Larger in Size. Diagn Cytopathol. 2015;43:622-8.
  • 51
    Aschebrook-Kilfoy B, Ward MH, Sabra MM, Devesa SS. Thyroid cancer incidence patterns in the United States by histologic type, 1992-2006. Thyroid. 2011;21:125-34.
  • 52
    Spencer C, LoPresti J, Fatemi S. How sensitive (second-generation) thyroglobulin measurement is changing paradigms for monitoring patients with differentiated thyroid cancer, in the absence or presence of thyroglobulin autoantibodies. Curr Opin Endocrinol Diabetes Obes. 2014;21:394-404.
  • 53
    Xavier AC, Maciel RM, Vieira JG, Dias-da-Silva MR, Martins JR. Insights into the posttranslational structural heterogeneity of thyroglobulin and its role in the development, diagnosis, and management of benign and malignant thyroid diseases. Arch Endocrinol Metab. 2016;60:66-75.

Publication Dates

  • Publication in this collection
    03 July 2023
  • Date of issue
    2023

History

  • Received
    07 Sept 2022
  • Accepted
    04 Jan 2023
Sociedade Brasileira de Endocrinologia e Metabologia Rua Botucatu, 572 - Conjuntos 81/83, 04023-061 São Paulo SP Brasil, Tel: (55 11) 5575-0311 - São Paulo - SP - Brazil
E-mail: aem.editorial.office@endocrino.org.br