We aimed to evaluate the diagnostic performance of thyroid ultrasonography (US) in each category of the Bethesda system and analyze false positive/negative findings using US. This retrospective study included 622 thyroid nodules in 592 patients. The sensitivity, specificity, negative predictive value (NPV), positive predictive value (PPV) and accuracy of US in each category of the Bethesda system were evaluated. False positive/negative cases of US were analyzed. Out of the 622 total thyroid FNAs, 179 (28.8%) were malignant. The malignancy rates for the 6 categories were as follows: I (nondiagnostic): 9.7%, II (benign): 2.5%, III (atypia/follicular lesion of undetermined significance): 37.5%, IV (suspicious for follicular neoplasm): 5.7%, V (suspicious for malignancy): 100%, and VI (malignancy): 100%. The accuracies of US for the 6 categories were 92.5%, 95.6%, 70.8%, 94.3%, 95%, and 92.4% in category order. US showed the lowest sensitivity (50%) in Category IV. Category III demonstrated relatively low sensitivity (66.7%) and specificity (73.3%) due to a high incidence of follicular variant of papillary thyroid carcinoma and a low number of category III nodules. The most optimal performance of US was revealed in Category I with 88.9% sensitivity and 92.9% specificity. In 22 US false positive cases, the most frequent finding was associated with marked hypoechogenicity and the least finding was noncircumscribed margin. The most common US features of 19 false negative cases were circumscribed iso or hypoechoic nodules. These results highlight the excellent diagnostic performance of US in category I of the Bethesda system and the lowest sensitivity of US in category IV. Awareness of US interpreters regarding these pitfalls can minimize false positive/negative diagnoses and prevent unnecessary interventions.
Citation: Park SY, Hahn SY, Shin JH, Ko EY, Oh YL (2016) The Diagnostic Performance of Thyroid US in Each Category of the Bethesda System for Reporting Thyroid Cytopathology. PLoS ONE 11(6): e0155898. https://doi.org/10.1371/journal.pone.0155898
Editor: Giancarlo Troncone, University of Naples Federico II, Naples, Italy, ITALY
Received: December 3, 2015; Accepted: May 5, 2016; Published: June 27, 2016
Copyright: © 2016 Park et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data are available from Figshare at the following link: https://figshare.com/s/86811c8d1fedad520a4d.
Funding: Authors are affiliated with Samsung Medical Centre, which is a part of the Samsung Group. Authors receive salaries as employees of Samsung Medical Centre.
Competing interests: Authors are affiliated with Samsung Medical Centre, which is a part of the Samsung Group.
Thyroid ultrasound (US) is the mainstay technique by which thyroid nodules are evaluated. Moreover, a general consensus has now been reached regarding the best US criteria for differentiating benign from malignant nodules [1–3]. The established US features of a malignant nodule include a taller-than-wide shape, an irregular margin, microcalcifications, and marked hypoechogenicity [2,4,5]. Ultrasound-guided fine needle aspiration (FNA) for suspicious thyroid nodules is an accurate and widely used diagnostic method. Cytological results can indicate whether surgery or follow-up is most appropriate for the thyroid nodules. The Bethesda System for Reporting Thyroid Cytopathology (BSRTC) was developed in 2009 to standardize the terminology for interpreting aspiration cytology results [6–8]. The application of BSRTC improved diagnostic accuracy for indeterminate thyroid nodules, leading to higher rates of malignancy detection despite lower rates of thyroidectomies . To manage thyroid nodules, clinicians typically receive two kinds of categorical reports: morphological category, which is based on US, and cytological category, which is based on FNA. It is not yet known whether ultrasound diagnoses have limitations for any of the BSRTC categories, or whether they can provide helpful information for some cytological results. Thus, the purpose of our study was to evaluate the diagnostic performance of thyroid US in each category of the Bethesda System for Reporting Thyroid Cytopathology and analyze false positive/negative findings using US.
Materials and Methods
This retrospective study was approved by the institutional review board of Samsung Medical Center and the requirement for informed consent was waived. This study included thyroid nodules assessed by US-guided FNA between Aug. and Oct. 2010 at our institution. Our institution served about average 8000 US-guided FNAs per year by radiologists at the study period. Generally, it seems that incidence of the malignancy of thyroid nodules by FNAs performed in our hospital is about 25–30%. This incidence rate is relatively high because our hospital is a tertiary referral center. All nodules were categorized based on the Bethesda system. We retrospectively reviewed the pathology and US reports of each patient. Patient records were analyzed anonymously. A total of 1353 FNAs in 1345 patients were performed during the study period. From these, nonthyroidal lesion (n = 93), nodules smaller than 0.5cm (n = 155), and nodules with no acceptable follow-up or operation (n = 483) were excluded. Finally, 622 nodules were selected from 592 patients who were followed up for at least 2 years or underwent surgery. Statistical analysis was performed on these 622 thyroid nodules.
Thyroid Ultrasound and Image Analysis
Thyroid US was performed at a frequency range of 7 to 15 MHz on an iU22 (Vision 2010; Philips, Seattle, WA, USA) by one of 7 radiologists. All radiologists had 1 to 11 years of experience in thyroid imaging.
The US features of the thyroid nodules were prospectively analyzed by the radiologist who performed the US examination. All nodules were classified into one of three categories (benign, indeterminate, and malignant) according to the Korea Society of Thyroid Radiology (KSThR) guidelines . The KSThR guidelines take into account the internal components, echogenicity, margin, calcification, shape, and orientation of the thyroid nodule and categorized thyroid nodules in to three US diagnosis (Table 1). A taller-than-wide shape, a spiculated or irregular margin, marked hypoechogenicity, microcalcifications, and macrocalcifications are all findings suggestive of malignancy . The presence of at least one of these findings defined a nodule as a malignant nodule. In contrast, simple cysts, predominantly cystic or cystic nodules with reverberating artifacts, and nodules with a spongiform appearance (especially with intervening isoechoic parenchyma) were defined as benign nodules. Indeterminate nodules had neither malignant nor benign features; iso-, hypo- or hyperechogenecity, ovoid-to-round shape, irregular shape, smooth or ill-defined margin, and rim calcification.
US-FNA was performed by one of the seven trained radiologists who conducted the US examinations. US-FNA was performed manually with a 23-gauge needle attached to a 2-mL disposable syringe. On average, 1–2 passes were performed for each nodule. Aspirates were smeared onto a glass slide,immediately fixed in 95% alcohol for Papanicolaou and hematoxylin and eosin staining. No Giemsa stain, liquid-based cytology or cytobloc were performed. One of six cytopathologists interpreted the FNA specimens. All cases were reported using a six-tiered diagnostic system according to the Bethesda System for Reporting Thyroid Cytopathology . Nodules were classified into the following cytological categories: (1) nondiagnostic or unsatisfactory (Bethesda System I), (2) benign (Bethesda System II), (3) atypia of undetermined significance (AUS)/follicular lesion of undetermined significance (FLUS) (Bethesda System III), (4) follicular neoplasm or suspicious for a follicular neoplasm (Bethesda System IV), (5) suspicious for malignancy (Bethesda System V), and (6) malignant (Bethesda System VI).
Data and Statistical Analysis
All thyroid nodules were categorized according to their US features and also according to their cytopathologic results. Although nodules were classified into three groups according to their US results, nodules identified as indeterminate by US were treated as benign for all subsequent statistical analysis. Thus, statistical analysis was performed on two US categories, probably benign and malignant.
Lesions were considered to be cytopathologically benign if they met at least one of the following conditions: 1] pathologically confirmed as benign by thyroidectomy or core needle biopsy; 2] US follow-up for at least 2 years with either no interval change or a decrease in size after an initial benign cytology finding; and 3] benign cytology by more than two FNAs. Nodules were defined as malignant if they were confirmed as malignant thyroid carcinoma by two serial FNAs or by thyroidectomy.
Data were analyzed using the Statistical Package for the Social Sciences for Windows (Version 17.0.1, SPSS, Chicago, IL, USA). In each category of the Bethesda system, the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy of ultrasonography were calculated using the McNemar test. Fisher's Exact Test for Count Data was used to determine whether the differences in accuracy between the 6 Bethesda groups were significant. A P value < 0.05 was considered to be statistically significant.
A total of 592 patients with 622 thyroid nodules (male: 119, female: 473) were included in this study. The mean age was 49.8 years old (range, 14–86 years) and the mean nodule size was 1.61 cm (range, 0.6–7.0cm).
Among all 1105 thyroid nodules which underwent FNA with or without follow up or surgery, the distribution of the Bethesda category was as follows: 163 (14.8%) in category I, 651 (58.9%) in category II, 37 (3.3%) in category III, 45 (4.1%) in category IV, 30 (2.7%) in category V and 179 (16.2%) in category VI. Among them, 622 thyroid nodules which were finally included in statistical analysis were classified into the Bethesda categories as follows: 93 (15.0%) in category I, 319 (51.3%) in category II, 24 (3.9%) in category III, 35 (5.6%) in category IV, 20 (3.2%) in category V, and 131 (21.0%) in category VI.
The proportions of US diagnoses (benign, indeterminate, and malignant) in each Bethesda category are listed in Table 2 (Fig 1). In total, 440 (70.7%) thyroid nodules were classified as probably benign by US (“US probably benign”) and 182 (29.3%) thyroid nodules were malignant by US (“US malignant”). Out of all the US probably benign nodules, 68.9% (303/440) were classified in Bethesda category II. Out of the 622 thyroid nodules, 182 (29.3%) were ultimately classified as US malignant. Out of all the US malignant nodules, 66.5% (121/182) were classified in Bethesda category VI and 76.9% (140/182) were classified in Bethesda category V and VI.
(a) Axial view show microlobulated isoechoic nodule with microcalcifications. (b) Sagittal view show a 1.3 cm microlobulated isoechoic nodule with microcalcifications (crosses) in the mid portion of the right thyroid gland. The US diagnosis was malignant and the FNA result was Bethesda category I (non-diagnostic). Total thyroidectomy was performed and the pathological result was papillary thyroid cancer. US was highly sensitive in identifying nodules diagnosed as Bethesda category I.
Classification of a nodule as benign was determined by operation or core needle biopsy in 55 nodules, two FNAs in 112 nodules, and US follow-up after FNA with benign result in 276 nodules. Of the malignant nodules, 172 were confirmed by surgery and 7 were confirmed by two serial FNAs or core needle biopsy. These 3 patients did not undergo surgery due to refusal of the operation and having aggressive malignancy of another organ. Out of the 179 malignant nodules, 171 were papillary thyroid carcinomas (PTC), 4 were follicular thyroid carcinoma (FTC). 2 were medullary thyroid carcinoma (MTC) and 2 were diffuse large B-cell lymphoma.
The final cytopathological results in each Bethesda category are shown in Table 3. The malignant rates for the 6 categories were as follows: Bethesda System I: 9.7% (9/93), Bethesda System II: 2.5% (8/319), Bethesda System III: 37.5% (9/24), Bethesda System IV: 5.7% (2/35), Bethesda System V: 100% (20/20), and Bethesda System VI: 100% (131/131) (Fig 2). All Bethesda category V and VI nodules were ultimately classified as malignant, with no false positives detected.
(a) Axial view show a circumscribed isoechoic nodule (crosses). (b) Sagittal view a 2.9 cm circumscribed isoechoic nodule (crosses) is visible in the lower portion of the right thyroid gland. The US diagnosis was probably benign and the FNA result was Bethesda category IV (follicular neoplasm). Follicular thyroid carcinoma was revealed by total thyroidectomy. US was not informative for this Bethesda category IV nodule.
We calculated the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy of the US diagnosis in each Bethesda category (Table 4). The sensitivities of US in categories I, V and VI were 88.9%, 95% and 92.4%, respectively, while the sensitivities in categories II, III and IV were 62.5%, 66.7% and 50%, respectively. The US showed the lowest sensitivity in Category IV. The specificity was also high in Bethesda category I (92.9%) and could not calculate the specificity of category V and VI because all Category V and VI thyroid nodules were final malignant. The specificities were also high in category II and IV, 96.5% and 97.0%, respectively but relatively low in Bethesda category III (73.3%). PPVs were 100% in category V and VI and those of other categories were less than 60%. NPVs were high in category I, II and IV, 98.8%, 99.0% and 97.0%, respectively. The accuracies of US for the 6 categories were 92.5%, 95.6%, 70.8%, 94.3%, 95.0%, and 92.4% (in category order). The most optimal performance of US was revealed in Category I with 88.9% sensitivity and 92.9% specificity.
False positive cases which were considered malignant on US were 22. The most frequent finding was associated with marked hypoechogenicity and the least finding was noncircumscribed margin. Thirteen (59%) of 22 had only one suspicious feature. False negative cases were 19. The reasons for FNA in 19 false negative US cases confirmed later were as follows; nodules larger than 1cm with US indeterminate (11 cases), interval increased size (6 cases), and PET uptakes (2 cases). Three FTCs showed probably benign US features and FNA results were Category I, II and IV. The PTC arising from follicular adenoma, 4 follicular variants of PTC showed probably benign US features and FNA results were Category II and III. Eleven PTCs with FNA results V and VI showed probably benign US features. The most common features of false negative showed circumscribed iso or hypoechoic nodules.
Thyroid US and US-guided FNA are the two leading diagnostic tools for evaluating thyroid nodular disease. The decision of whether to conduct surgery or to perform follow-up is taken based on thyroid US results together with cytological findings .
Due to the lack of information regarding the extent to which US and cytological reports are correlated, it may be difficult for physicians and surgeons to make treatment decisions. Several studies have evaluated the extent to which US diagnoses correlate with cytological results [11–16]. Lee at al. evaluated the usefulness of a combined categorical reporting system, including both US and cytological results, for deciding when repeat US-guided FNA should be performed . Some investigators reported the incidence of thyroid cancer among cases with non-diagnostic (Bethesda category I) cytology and additionally evaluated the criteria for selecting those for repeat FNA according to US features [12,16]. Kim et al. and Rosario et al. reported the diagnostic efficacy of US in evaluating thyroid nodules, especially for Bethesda category III nodules [13,15]. In our study, we evaluated the diagnostic performance of US in each of the 6 Bethesda categories.
In our study, US showed the most optimal performance in Bethesda category I with a sensitivity of 88.9% and a specificity of 92.9%. Only one Bethesda category I nodule with the confirmation as FTC after operation was counted as false negative in US. This finding indicated that US can play an important role in determining further management for cytologically non-diagnostic thyroid nodules. Specifically, US follow-up rather than re-aspiration is recommended for US benign-looking nodules with Bethesda I results according to high sensitivity, specificity and accuracy of US in Bethesda category I thyroid nodules. This recommendation is consistent with that of Lee et al., who also recommended follow-up for US benign non-diagnostic nodules. This conclusion was based on the high possibility of other non-diagnostic FNA results, which are of little clinical relevance . Moon et al. also recommended follow up rather than re-aspiration if Bethesda category I nodules have one or less suspicious US feature or nodules with cystic portion greater than 50% .
Bethesda category III is cytologically indeterminate and its rate of malignancy has been reported to range from 5–22.6% [15,17]. The recommended management for category III is clinical correlation and a repeated FNA at an appropriate interval. However, many reports have cited a risk of malignancy that should be considered in the management of Bethesda III nodules. This risk depends on the particular physician and institution and is influenced by clinical observations, repeat FNAs, core-needle biopsies, and surgeries [15,17]. To overcome the diagnostic limitations of cytology in indeterminate categories, many studies have evaluated the ability of thyroid US to predict malignancy for Bethesda category III nodules, with the aim of identifying management guidelines for these lesions [2,17–20]. In our study, US had a sensitivity of 66.7%, a specificity of 73.3%, a PPV of 60.0%, and an NPV of 78.6% in Bethesda category III nodules. Rosario et al. recently reported prospective study for clinical, laboratory, ultrasonographic, and cytological predictors of malignancy in Bethesda category III thyroid nodules. US sensitivity, specificity, PPV and NPV were 79.4%, 90.5%, 71% and 93.5%, respectively . Several other studies also suggested the usefulness of US for evaluating malignancy of Category III nodules [11,13,17]. Sensitivity and specificity were relatively low in our study compared to previous studies, probably because of low number of category III nodules (4.8%). Three category III nodules showed false negative result of US which led to relatively low sensitivity in our study, and all those 3 nodules were follicular variant of PTC. Follicular variants of PTC are reported to have relatively benign appearance on sonography that is more similar to those of follicular neoplasm than PTCs and this might be the reason of false negative US findings .
The accuracies of US in Bethesda categories III is relatively low (70.8%) compared to that of Category I (92.5%), II (95.6%), IV (94.3%), V (95.0%) and VI (92.4%). We speculate that the low accuracy of US in Bethesda category III nodules resulted from our classification of US indeterminate nodules treated as US probably benign nodules. If US indeterminate nodules would have been considered to be US malignant nodules, better sensitivity and accuracy would have been achieved. However, in contrast to nodules with malignant features, US indeterminate nodules should not be managed under strict guidelines because most thyroid carcinomas are not aggressive and have a good prognosis.
Meanwhile, the sensitivity and PPV in categories IV were 50% and 50%, respectively. Although the specificities and NPVs of US for nodules with cytologically suspicious for follicular neoplasm (IV) were high. This result indicates that the current US morphologic guidelines for follicular neoplasm are of limited value. The current US features mainly reflect papillary thyroid cancer, which limits the sensitivity of US in Bethesda category IV nodules. Further studies with pathology-radiology correlation are needed for follicular neoplasm of thyroid gland.
Among 22 false positive cases at US, the most frequent finding was marked hypoechogenicity and the least finding was noncircumscribed margin. Major reason for false positive cases was because nodules were interpreted as marked hypoechoic due to uncontrolled sonic gain. At follow-up of these nodules, they were not marked hypoechoic under control of proper gain. Careful adjustment of sonic gain is crucial for appropriate diagnosis of thyroid nodule and increase the efficacy of US. Benign thyroid nodules showed irregular or noncircumscribed margin when previously existing fluid component had disappeared causing shrinkage of thyroid nodules.
Comparing the 2011 KSThR guidelines to 2015 American thyroid association (ATA) guidelines, KSThR US “probable benign” correlates to US “very low suspicion” and “benign” of ATA guidelines. KSThR US “indeterminate” correlates to US “intermediate suspicion” and “low suspicion” of ATA. KSThR US “suspicious malignant” correlates to “high suspicion” of ATA. The major difference between two guidelines divided indeterminate and probable benign categories into more detailed categorizations. ATA recommended FNA at different size in “intermediate suspicion” and “low suspicion” (> 1cm and > 1.5cm, respectively), whereas KSThR recommended FNA in US “suspicious malignant”nodules > 0.5cm and US indeterminate nodules ≥ 1cm. Another difference is emphasizing rim calcified lesion. KSThR guidelines categorized rim calcified nodules into indeterminate category and commented that the presence of a hypoechoic halo and rim disruption are more suggestive of malignancy. In ATA guidelines, rim calcified nodules with small extrusive soft tissue component were categorized into “high suspicious” category. The other difference is macrocalcifications. KSThR guidelines categorized macrocalcifications as US “suspicious malignant”. In ATA guidelines, macrocalcifications have same malignancy risk as microcalcifications if they are combined with microcalcifications [2,22].
Our present study did not investigate the genetic abnormalities of thyroid nodules. Many investigators have reported that detection of RET/PTC, TRK and BRAF(V600E) in FNAB specimens is proposed as a diagnostic adjunctive tool in the evaluation of thyroid nodules with suspicious cytological findings. [23–25]. The combination of US findings, biopsy and genetic study is the most reliable triage as the current options for the evaluation of undetermined thyroid nodules.
Our study did have several limitations. First, this was a retrospective study based on radiologic and pathologic reports. Second, the US and FNA analyses of the 622 nodules were not performed by a single radiologist. Although all the radiologists who performed the US and FNA analyses were extensively trained, inter-assessor variation could have led to different US findings for nodules that are not easily classified. We did not calculate the interobserver variability between individuals. However, we have a system that can minimize the difference. Unexperienced (less than 2 years) radiologists have received the confirmation about all cases with equivocal or indeterminate US features from experienced radiologists in the next room or in real time. Each radiologist has a chance to control the threshold through intradepartment conference. Moreover, differences in FNA skill levels could have increased the number of non-diagnostic results. However, this scenario is representative of clinical practice.
In conclusion, these results highlight the excellent diagnostic performance of US in category I of the Bethesda system and the lowest sensitivity of US in category IV. Awareness of US interpreters regarding these pitfalls can minimize false positive/negative diagnoses and prevent unnecessary interventions.
Conceived and designed the experiments: SYP JHS SYH EYK YLO. Performed the experiments: SYP JHS SYH EYK YLO. Analyzed the data: SYP JHS SYH EYK YLO. Contributed reagents/materials/analysis tools: SYP JHS SYH EYK YLO. Wrote the paper: SYP JHS SYH EYK YLO.
- 1. Cooper DS, Doherty GM, Haugen BR, Kloos RT, Lee SL, Mandel SJ, et al. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 2009;19: 1167–1214. pmid:19860577
- 2. Moon WJ, Baek JH, Jung SL, Kim DW, Kim EK, Kim JY, et al. Ultrasonography and the ultrasound-based management of thyroid nodules: consensus statement and recommendations. Korean J Radiol. 2011;12: 1–14. pmid:21228935
- 3. Gharib H, Papini E, Paschke R, Duick DS, Valcavi R, Hegedus L, et al. American Association of Clinical Endocrinologists, Associazione Medici Endocrinologi, and European Thyroid Association medical guidelines for clinical practice for the diagnosis and management of thyroid nodules: executive summary of recommendations. J Endocrinol Invest. 2010;33: 51–56. pmid:20543551
- 4. Frates MC, Benson CB, Charboneau JW, Cibas ES, Clark OH, Coleman BG, et al. Management of thyroid nodules detected at US: Society of Radiologists in Ultrasound consensus conference statement. Radiology. 2005;237: 794–800. pmid:16304103
- 5. Kwak JY, Jung I, Baek JH, Baek SM, Choi N, Choi YJ, et al. Image reporting and characterization system for ultrasound features of thyroid nodules: multicentric Korean retrospective study. Korean J Radiol. 2013;14: 110–117. pmid:23323040
- 6. Cibas ES, Ali SZ. The Bethesda System For Reporting Thyroid Cytopathology. Am J Clin Pathol. 2009;132: 658–665. pmid:19846805
- 7. Crowe A, Linder A, Hameed O, Salih C, Roberson J, Gidley J, et al. The impact of implementation of the Bethesda System for Reporting Thyroid Cytopathology on the quality of reporting, "risk" of malignancy, surgical rate, and rate of frozen sections requested for thyroid lesions. Cancer Cytopathol. 2011;119: 315–321. pmid:21751427
- 8. Rabaglia JL, Kabbani W, Wallace L, Holt S, Watumull L, Pruitt J, et al. Effect of the Bethesda system for reporting thyroid cytopathology on thyroidectomy rates and malignancy risk in cytologically indeterminate lesions. Surgery. 2010;148: 1267–1272; discussion 1272–1273. pmid:21134560
- 9. Hirsch D, Robenshtok E, Bachar G, Braslavsky D, Benbassat C. The Implementation of the Bethesda System for Reporting Thyroid Cytopathology Improves Malignancy Detection Despite Lower Rate of Thyroidectomy in Indeterminate Nodules. World J Surg. 2015;39: 1959–1965. pmid:25809059
- 10. Szczepanek-Parulska E, Wolinski K, Stangierski A, Gurgul E, Biczysko M, Majewski P, et al. Comparison of diagnostic value of conventional ultrasonography and shear wave elastography in the prediction of thyroid lesions malignancy. PLoS One. 2013;8: e81532. pmid:24312313
- 11. Lee SW, Lee HJ, Kim HJ, Lee J, Park JY, Kim SH, et al. Combined categorical reporting systems of US and cytology findings for thyroid nodules: guidance on repeat fine-needle aspiration cytology. Radiology. 2013;266: 956–963. pmid:23220892
- 12. Chung J, Youk JH, Kim JA, Kwak JY, Kim EK, Ryu YH, et al. Initially non-diagnostic ultrasound-guided fine needle aspiration cytology of thyroid nodules: value and management. Acta Radiol. 2012;53: 168–173. pmid:21969700
- 13. Kim DW, Lee EJ, Jung SJ, Ryu JH, Kim YM. Role of sonographic diagnosis in managing Bethesda class III nodules. AJNR Am J Neuroradiol. 2011;32: 2136–2141. pmid:21920860
- 14. Moon HJ, Kim EK, Kwak JY. Malignancy risk stratification in thyroid nodules with benign results on cytology: combination of thyroid imaging reporting and data system and Bethesda system. Ann Surg Oncol. 2014;21: 1898–1903. pmid:24558069
- 15. Rosario PW. Thyroid nodules with atypia or follicular lesions of undetermined significance (Bethesda Category III): importance of ultrasonography and cytological subcategory. Thyroid. 2014;24: 1115–1120. pmid:24684285
- 16. Moon HJ, Kim EK, Yoon JH, Kwak JY. Malignancy risk stratification in thyroid nodules with nondiagnostic results at cytologic examination: combination of thyroid imaging reporting and data system and the Bethesda System. Radiology. 2015;274: 287–295. pmid:25133852
- 17. Gweon HM, Son EJ, Youk JH, Kim JA. Thyroid Nodules with Bethesda System III Cytology: Can Ultrasonography Guide the Next Step? Ann Surg Oncol. 2013;20: 3083–3088. pmid:23700214
- 18. Broome JT, Solorzano CC. The impact of atypia/follicular lesion of undetermined significance on the rate of malignancy in thyroid fine-needle aspiration: evaluation of the Bethesda System for Reporting Thyroid Cytopathology. Surgery. 2011;150: 1234–1241. pmid:22136846
- 19. Maia FF, Matos PS, Pavin EJ, Vassallo J, Zantut-Wittmann DE. Value of repeat ultrasound-guided fine-needle aspiration in thyroid nodule with a first benign cytologic result: impact of ultrasound to predict malignancy. Endocrine. 2011;40: 290–296. pmid:21499817
- 20. Onder S, Firat P, Ates D. The Bethesda system for reporting thyroid cytopathology: an institutional experience of the outcome of indeterminate categories. Cytopathology. 2014;25: 177–184. pmid:23998291
- 21. Rhee SJ, Hahn SY, Ko ES, Ryu JW, Ko EY, Shin JH. Follicular variant of papillary thyroid carcinoma: distinct biologic behavior based on ultrasonographic features. Thyroid. 2014;24: 683–688. pmid:24341498
- 22. 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. pmid:26462967
- 23. Nam SY, Han BK, Ko EY, Kang SS, Hahn SY, Hwang JY, et al. BRAF V600E mutation analysis of thyroid nodules needle aspirates in relation to their ultrasongraphic classification: a potential guide for selection of samples for molecular analysis. Thyroid. 2010;20:273–279. pmid:20187782
- 24. Kim TH, Jeong DJ, Hahn SY, Shin JH, Oh YL, Ki CS, et al. Triage of patients with AUS/FLUS on thyroid cytopathology: effectiveness of the multimodal diagnostic techniques. Cancer Med. 2016 Jan 18.
- 25. Sapio MR, Posca D, Raggioli A, Guerra A, Marotta V, Deandrea M, et al. Detection of RET/PTC, TRK and BRAF mutations in preoperative diagnosis of thyroid nodules with indeterminate cytological findings. Clin Endocrinol (Oxf). 2007;66:678–683.