Back to Journals » Cancer Management and Research » Volume 12

Hounsfield Unit Values in ACR TI-RADS 4-5 Thyroid Nodules with Coarse Calcifications: An Important Imaging Feature Helpful for Diagnosis

Authors Wei PY, Jiang ND, Xiang JJ, Xu CK, Ding JW, Wang HB, Luo DC , Han ZJ

Received 16 December 2019

Accepted for publication 2 April 2020

Published 22 April 2020 Volume 2020:12 Pages 2711—2717

DOI https://doi.org/10.2147/CMAR.S242524

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Antonella D'Anneo



Pei-Ying Wei,1,* Nian-Dong Jiang,2,* Jing-Jing Xiang,3 Chen-Ke Xu,4 Jin-Wang Ding,5 Hai-Bin Wang,1 Ding-Cun Luo,5 Zhi-Jiang Han1

1Department of Radiology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, People’s Republic of China; 2Department of Radiology, Chunan County Hospital of Traditional Chinese Medicine, Hangzhou, People’s Republic of China; 3Department of Pathology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, People’s Republic of China; 4Department of Medical Ultrasound, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, People’s Republic of China; 5Department of Surgical Oncology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Zhi-Jiang Han Email [email protected]

Purpose: The purpose of this study is to investigate the diagnostic role of Hounsfield unit (HU) values on noncontrast computed tomography (CT) for differentiating benignity from malignancy in the American College of Radiology (ACR) Thyroid Imaging Reporting and Data System (TI-RADS) 4-5 nodules with coarse calcifications.
Patients and Methods: CT images of 216 ACR TI-RADS 4-5 nodules with coarse calcifications from 207 patients who underwent surgery in our hospital between 2017 and 2019 were retrospectively reviewed. The average HU values (AHUVs) and maximum HU values (MHUVs) of the nodules were measured on noncontrast CT. The distribution of AHUVs and MHUVs in benign and malignant nodules with coarse calcifications was analyzed using the Mann–Whitney test. Receiver operating characteristic (ROC) curves were used to identify the best cut-off values. Diagnostic performances were assessed according to the area under the ROC curve (AUC), sensitivity and specificity.
Results: Of the 216 ACR TI-RADS 4-5 nodules with coarse calcifications, 170 were benign and 46 were malignant. The AHUVs of benign and malignant nodules were 791 HU [interquartile range (IQR), 543– 1025 HU] and 486 HU (IQR, 406– 670 HU), respectively (P < 0.001). The MHUVs of benign and malignant nodules were 1084 HU (IQR, 717– 1477 HU) and 677 HU (IQR, 441– 986 HU), respectively (P < 0.001). The AUCs for AHUVs and MHUVs for predicting benign nodules with coarse calcifications were 0.759 and 0.732, and the cut-off values were 627.5 HU and 806.0 HU, with sensitivities of 67.6% and 68.8% and specificities of 73.9% and 67.4%, respectively. The sensitivity and specificity of the combination were 68.8% and 76.1%.
Conclusion: AHUVs and MHUVs were helpful in differentiating benignity from malignancy in ACR TI-RADS 4-5 nodules with coarse calcifications. This may provide an important basis for reducing misdiagnosis and unnecessary aspiration or surgical trauma.

Keywords: thyroid nodule, coarse calcification, ACR TI-RADS, computed tomography, ultrasonography, Hounsfield unit value

Introduction

Thyroid nodules are exceedingly common, with a reported prevalence of 20–67% on ultrasound (US) examinations and up to 25% on contrast-enhanced thoracic computed tomography (CT) scans.1 Calcification is a common imaging finding observed in thyroid nodules, which accounts for 15.7–28.9% of benign nodules and 49.6–65.9% of malignant nodules on US examinations.2,3 The diagnostic value of microcalcifications for malignant nodules has been widely accepted.24 However, coarse calcifications often cause obvious echo attenuation, which affects the visualization of internal and posterior structures of the calcified nodules. Moreover, coarse calcifications are often accompanied by fibrosis in the surrounding area, which results in uneven echo and fails to provide sufficient information for proper diagnosis. Therefore, thyroid nodules with coarse calcifications are usually classified as the American College of Radiology (ACR) Thyroid Imaging Reporting and Data System (TI-RADS) 4 or 5,58 hence cause significant confusion among clinicians and patients, and even unnecessary surgical trauma.

Fine-needle aspiration (FNA) is often recommended for ACR TI-RADS 4 or 5 nodules,5,9,10 which is considered the most effective practical technique to reach a definitive diagnosis for most thyroid nodules.11,12 However, for thyroid nodules with coarse calcifications, particularly those with thick-walled annular calcifications, it is difficult to penetrate the hard calcified area or obtain sufficient cytology specimens, even if penetration is achieved.1315 This results in nondiagnostic and inconclusive rates on FNA up to 27.2–53.8% and 42.2–57.7%, respectively.15,16 Compared with FNA, coarse needle biopsy (CNB) is often able to obtain adequate cytological specimens with higher specificity.15,17 However, more traumas are involved with CNB procedures.

Although CT is inadequate for the diagnosis of microscopic and diffuse lesions in the thyroid, it is able to fully reveal the internal and surrounding structures of nodules with coarse calcifications due to the absence of echo attenuation. In our previous studies, we analyzed CT histogram characteristics and artifacts of solitary coarse calcified nodules respectively. We found that both the proportion of voxels < 1150 Hounsfield units (HU) no more than 98.4% and the presence of artifacts around calcifications on noncontrast CT could contribute to the diagnosis of benign nodules.18,19 However, the operation and analysis of CT histogram is complex and requires special measurement software, while evaluating artifact is a subjective process. Therefore, both are difficult to be widely applied. We suggest that HU value, similar to CT histogram and artifact, could also reflect the internal structure and density characteristics inside calcified nodules to a certain extent, from which their properties could be assessed.

To the best of our knowledge, no previous studies have investigated maximum Hounsfield unit values (MHUVs) of thyroid nodules with coarse calcifications on noncontrast CT. Based on our previous studies,1822 the present study aimed to explore the diagnostic role of average Hounsfield unit values (AHUVs) and MHUVs in ACR TI-RADS 4-5 nodules, so as to provide an important basis for further diagnosis and treatment in the clinic.

Patients and Methods

Patients

This study involved all patients with thyroid nodules who underwent surgery in our hospital between August 2017 and August 2019. The inclusion criteria were as follows: (1) ACR TI-RADS 4-5 thyroid nodules, (2) CT scan performed before surgery, (3) short diameter of the calcified area of nodule ≥ 4 mm and (4) pathological verification after surgery. The exclusion criteria were as follows: (1) nodules that were not clearly visible on CT images due to poor image quality or those with other thyroid diseases, and (2) patients with incomplete clinical and imaging data. Ultimately, a total of 207 patients (36 males and 171 females, aged 54.0 ± 11.0 years, range 28–82 years) with 216 thyroid coarse calcified nodules were included in the study. This retrospective study was approved by the Ethics Committee of the Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine (Hangzhou, Zhejiang Province, People’s Republic of China). Due to the retrospective nature of the study and the use of anonymized patient data, written informed consent for participation was not required, in accordance with the national legislation and institutional requirements.

Pathology

All 216 ACR TI-RADS 4-5 thyroid nodules with coarse calcifications from the 207 patients had a conclusive pathological diagnosis confirmed by senior pathologists. Archived tissue specimens were cut into sections (5 μm thick) and fixed in 10% neutral formalin and stained using the hematoxylin and eosin method. The tissue sections were then examined under a light microscope.

CT Examination

All patients underwent CT using a 16-slice spiral CT scanner (Lightspeed, GE Healthcare, Milwaukee, WI, USA). Patients were positioned supine and scanned from the base of the skull to the upper edge of the aortic arch. The scan parameters were as follows: power, 120 kV; current, 250 mA; collimation, 0.625 mm × l6 mm; and pitch, 0.938. The rotation time of the rack was 0.5 s and reconstruction thickness (ie, slice thickness) was 3.75 mm.

Image Analysis

CT images were reviewed independently by two radiologists (PYW and NDJ) with 5 and 8 years’ working experience, respectively. The radiologists were blinded to clinical information, other imaging results, and pathological data of the patients. They measured the HU values of nodules on the Picture Archiving and Communication Systems Workstation. The CT value of the calcified area was measured under soft tissue window width (WW) and window position (WL) (WW: 350, WL: 40). A round or elliptical area was used to delineate the region of interest (ROI). For measuring AHUV, the ROI should be as large as possible and avoid the non-calcified area. The HU values in the maximum and sub-maximal sections of the calcified area were measured, from which the larger was selected (Figure 1A and B). For measuring MHUV, the ROI should extend beyond the edge of each section of calcified area, and avoid covering other calcifications outside the nodules or the surrounding bone structure. The maximum measurement result was considered the MHUV of nodule (Figure 2A and B). The AHUVs and MHUVs measured by the two radiologists respectively were taken for interobserver consistency analysis. The mean values of AHUVs and MHUVs measured by the two radiologists were used for analysis of diagnostic performances.

Figure 1 Method for measuring AHUV. Notes: (A) AHUV of the nodule was 879.3 HU, and the nodule was surgically confirmed as nodular goiter. (B) AHUV of the nodule was 463.8 HU, and the nodule was surgically confirmed as papillary thyroid carcinoma.Abbreviation: AHUV, average Hounsfield unit value.

Figure 2 Method for measuring MHUV. Notes: (A) MHUV of the nodule was 1410.0 HU, and the pathology was nodular goiter. (B) MHUV of the nodule was 805.0 HU, and the pathology was papillary thyroid carcinoma. Abbreviation: MHUV, maximum Hounsfield unit value.

Statistical Analyses

Statistical analyses were performed using SPSS 19.0 (IBM Corporation, Armonk, NY, USA) and MedCalc 15.8 (MedCalc, Ostend, Belgium). Variables with normal distribution were expressed as mean ± standard deviation, while variables with non-normal distribution were expressed as median [interquartile range (IQR)]. Categorical variables were analyzed using the chi-squared test or the Fisher’s exact test, while continuous variables were compared using the independent samples t-test or the Wilcoxon rank sum test. Receiver operating characteristic (ROC) curves were used to analyze the diagnostic value of AHUVs and MHUVs. The best cut-off values were obtained from ROC analyses. Diagnostic performances were assessed according to the area under the ROC curve (AUC), sensitivity, and specificity. Cohen’s kappa coefficient was used to assess the consistency between the two radiologists. Differences with P < 0.05 were considered to be statistically significant.

Results

During the study period, a total of 207 patients with 216 ACR TI-RADS 4-5 thyroid nodules with coarse calcifications were enrolled according to the selection criteria. The typical US images are shown in Figure 3A and B. All 170 benign nodules with coarse calcifications from 163 patients were nodular goiters, while 45 malignant nodules from 44 patients were papillary thyroid carcinomas, and 1 nodule was follicular carcinoma. The typical pathological images are shown in Figure 4A and B. There were 25 males and 138 females with benign nodules, and 11 males and 33 females with malignant nodules. The mean age of the male patients was 55.95 ± 12.14 years and 53.48 ± 11.02 years for females. The average lesion size of benign and malignant nodules was 10.90 mm (IQR, 7.43–14.70 mm) and 8.70 mm (IQR, 6.80–13.00 mm), respectively. The sexes, ages and lesion sizes showed no significant differences between benign and malignant nodules. The AHUV for benign nodules was 791 HU (IQR, 543–1025 HU) and for malignant nodules was 486 HU (IQR, 406–670 HU). The MHUV for benign nodules was 1084 HU (IQR, 717–1477 HU) and for malignant nodules was 677 HU (IQR, 441–986 HU).The differences were significant in terms of AHUVs and MHUVs (Table 1).

Table 1 General Data and Hounsfield Unit Values

Figure 3 Typical ultrasound images for ACR TI-RADS 4−5 nodules with coarse calcifications, which revealed calcifications were interrupted, accompanied by significant echo attenuation in the posterior area. Notes: (A) The nodule was classified to ACR TI-RADS 4, and the pathology was nodular goiter. (B) The nodule was classified to ACR TI-RADS 5, and the pathology was papillary thyroid carcinoma. Abbreviation: ACR TI-RADS, the American College of Radiology Thyroid Imaging Reporting and Data System.

Figure 4 Typical pathological images. Notes: (A) Pathological image (original magnification ×20) of nodular goiter revealing that calcifications (black arrow) surrounded by fibrosis (white arrow). (B) Pathological image (original magnification ×30) of papillary thyroid carcinoma revealing calcifications (black arrow) and fibrosis (white arrow) separated by cancer tissues (black pentagram).

For predicting the benign nodules with coarse calcifications, the AUCs for AHUVs and MHUVs were 0.759 (95% confidence interval [CI], 0.697–0.815) and 0.732 (95% CI, 0.667–0.790), respectively (Figure 5). When the maximum values of Jordan index for AHUVs and MHUVs were 0.415 and 0.362, the cut-off values were 627.5 HU and 806.0 HU, with sensitivities of 67.6% and 68.8%, specificities of 73.9% and 67.4%, respectively. The sensitivity and specificity of the combination were 68.8% and 76.1%.

Figure 5 ROC curves of AHUV and MHUV. Abbreviations: ROC, receiver operating characteristic; AHUV, average Hounsfield unit value; MHUV, maximum Hounsfield unit value.

The two radiologists demonstrated good agreement regarding AHUVs (k = 0.840; 95% CI, 0.738–0.925). The MHUVs measured by the two radiologists are all consistent (k = 1).

Discussion

To our knowledge, this was the first study to use AHUVs and MHUVs on noncontrast CT to analyze ACR TI-RADS 4−5 nodules with coarse calcifications. According to our measurement method, the two radiologists demonstrated good agreement regarding AHUVs, and MHUVs measured by the two radiologists are all consistent. Our results demonstrated that the AHUVs and MHUVs of benign nodules were significantly higher than those of malignant nodules. The AUCs of AHUVs and MHUVs for predicting benign nodules with coarse calcifications were similar (0.759 and 0.732, respectively) and the cut-off values were 627.5 HU and 806.0 HU, with sensitivities of 67.6% and 68.8%, and specificities of 73.9% and 67.4%, respectively. With the increase in AHUVs and MHUVs, the specificity for benign diagnosis increased. The combination of AHUV and MHUV could further improve the specificity.

Pathologically, there is significant difference between benign and malignant thyroid coarse calcifications. Most benign calcifications or ossifications are continuous and manifest as dense plates, blocks, strips, arcs, or nodules. The mechanism is associated with sufficient and mature accumulation of calcium salts. However, malignant coarse calcifications are distributed in loose, intermittent spots or dots, even in honeycomb shape. The mechanism is related to the insufficient accumulation of calcium salts and continuous destruction by malignant tumor cells during the accumulation process.18,19,23 Therefore, these pathological differences between benign and malignant coarse calcifications are reflected as different densities on plain film or CT imaging.

In 1958, Holtz and Powers first proposed that the density of thyroid benign calcifications was significantly higher than that of malignant calcifications in X-ray examinations.24 However, due to the limitations of imaging technologies at that time, further quantitative analysis was impossible. In 2015, we estimated the diagnostic value of CT artifacts for solitary coarse calcifications in thyroid nodules, and found that the presence of artifacts was more supportive of the diagnosis of benign nodules.18 However, there are shortcomings in judging artifacts, such as strong subjectivity. Yang et al analyzed 41 cases with thyroid solitary calcified nodules and 55 cases with solely coarse calcified surrounded by a low-density focus. They found that the amplification of lesions after contrast enhancement was an independent risk factor for cancer.25 However, the delineation of ROI and judgement of lesion size were not specifically addressed, and the lesion sizes were not quantified in their study. In 2017, Kim et al analyzed 42 malignant and 19 benign coarse calcified nodules according to HU values, and found that the HU values for thyroid benign calcified nodules were higher than those for malignant calcified nodules.26 However, their sample cohort was small, and they did not further determine a cut-off HU value or analyze diagnostic efficacy. The sample size of benign nodules in our study was larger than that reported by Kim et al.26 We proposed MHUV for the first time and evaluated the ACR TI-RADS 4-5 thyroid coarse calcified nodules together with AHUVs. Our results demonstrated that the AHUVs and MHUVs of benign nodules were significantly higher than those of malignant nodules.

To increase the repeatability of the experiment in the present study, we defined the measurement methods for AHUVs and MHUVs. Although there was good consistency between the two radiologists in the process of measuring AHUVs, the measurement process was relatively complex, especially regarding the size of the ROI and the selection of the measurement area. However, the measurement of MHUVs was relatively simple, and the ROI only needed to cover the entire calcified nodule. The results show MHUVs measured by the two radiologists were all consistent. Our results demonstrated that the diagnostic efficiency of AHUVs was just slightly better than that of MHUVs when the maximum Jordan index was considered. The combination of both could further improve the specificity. However, there were still some deficiencies in specificity. To reduce the rate of misdiagnosis, therefore, higher specificity is needed. When the specificities of both were 91.3%, the sensitivity of MHUV (36.5%) was higher than AHUV (31.2%).

Our results showed that AHUVs and MHUVs were of great value in differentiating benignity from malignancy in ACR TI-RADS 4-5 nodules with coarse calcifications. However, it should be noted that performing noncontrast CT is not routinely feasible for all thyroid diseases, especially for microscopic and diffuse lesions, since its soft tissue resolution is limited, and it is relatively expensive and may be associated to harmful effects (ie use of ionising radiation).

The present investigation had several limitations. First, selection bias was inevitable because this was a retrospective study and the data were obtained from a single medical institute. Second, the combination of multiple CT signs may be more valuable for the qualitative diagnosis of nodules with coarse calcifications. However, this investigation aimed to introduce the diagnostic role of AHUV and MHUV on noncontrast CT, and further study will be done in combination with other CT signs. Finally, because the slice thickness in the CT scans was 3.75 mm, to avoid the influence of partial volume effect, ACR TI-RADS 4-5 nodules with a short diameter of calcified area < 4 mm were not included. Hence, whether our results are applicable to these nodules needs further study with a larger sample size.

Conclusion

AHUVs and MHUVs were helpful in differentiating benignity from malignancy in ACR TI-RADS 4-5 nodules with coarse calcifications. The former demonstrated greater AUC and specificity, while the latter had higher sensitivity and was more convenient in operation. The combination of both could further improve the specificity. This may provide an important basis for reducing misdiagnosis and unnecessary aspiration or surgical trauma.

Ethics and Consent Statement

Ethics Committee of the Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine approved this study. Due to the retrospective nature of the study and the use of anonymized patient data, informed consent for participation was not required, in accordance with the national legislation and institutional requirements.

Acknowledgments

This work was supported by Medical Science Research Program of Zhejiang Province (2020369811), Hangzhou Social Development Project of Science and Technology Commission (20180533B39), Applied Research Project of Commonweal Technology in Zhejiang Province (2017C33180), the Key Project of Scientific and Technological Innovation in Hangzhou (20131813A08), and Medicine Research Center, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province (2020E10021), for which the authors are grateful. We are very grateful to the editor and reviewers.

Author Contributions

All authors made substantial contributions to conception and design, acquisition of data, analysis and interpretation of data, drafting or revising the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.

References

1. Fisher SB, Perrier ND. The incidental thyroid nodule. CA Cancer J Clin. 2018;68:97−105.

2. Lu Z, Mu Y, Zhu H, et al. Clinical value of using ultrasound to assess calcification patterns in thyroid nodules. World J Surg. 2011;35:122−127. doi:10.1007/s00268-010-0827-3

3. Shi C, Li S, Shi T, et al. Correlation between thyroid nodule calcification morphology on ultrasound and thyroid carcinoma. J Int Med Res. 2012;40:350−357. doi:10.1177/147323001204000136

4. Ning CP, Ji QL, Fang SB, et al. Distribution patterns of microcalcifications in suspected thyroid carcinoma: a classification method helpful for diagnosis. Eur Radiol. 2018;28:1−8. doi:10.1007/s00330-017-5212-2

5. Tessler FN, Middleton WD, Grant EG, et al. ACR Thyroid Imaging, Reporting and Data System (TI-RADS): white paper of the ACR TI-RADS committee. J Am Coll Radiol. 2017;14:587−595. doi:10.1016/j.jacr.2017.01.046

6. Tappouni RR, Itri JN, McQueen TS, et al. ACR TI-RADS: pitfalls, solutions, and future directions. Radiographics. 2019;39:2040−2052. doi:10.1148/rg.2019190026

7. Grant EG, Tessler FN, Hoang JK, et al. Thyroid ultrasound reporting lexicon: white paper of the ACR thyroid imaging, reporting and data system (TIRADS) committee. J Am Coll Radiol. 2015;12:1272−1279. doi:10.1016/j.jacr.2015.07.011

8. Lyu YJ, Shen F, Yan Y, et al. Ultrasound-guided fine-needle aspiration biopsy of thyroid nodules <10 mm in the maximum diameter: does size matter? Cancer Manag Res. 2019;11:1231–1236. doi:10.2147/CMAR.S189358

9. Shen Y, Liu M, He J, et al. Comparison of different risk-stratification systems for the diagnosis of benign and malignant thyroid nodules. Front Oncol. 2019;9:378. doi:10.3389/fonc.2019.00378

10. Castellana M, Castellana C, Treglia G, et al. Performance of five ultrasound risk stratification systems in selecting thyroid nodules for FNA. A meta-analysis. J Clin Endocrinol Metab. 2019.

11. Singh Ospina N, Brito JP, Maraka S, et al. Diagnostic accuracy of ultrasound-guided fine needle aspiration biopsy for thyroid malignancy: systematic review and meta-analysis. Endocrine. 2016;53:651−661. doi:10.1007/s12020-016-0921-x

12. Lee J, Lee SY, Cha SH, et al. Fine-needle aspiration of thyroid nodules with macrocalcification. Thyroid. 2013;23:1106−1112. doi:10.1089/thy.2012.0406

13. Wu CW, Dionigi G, Lee KW, et al. Calcifications in thyroid nodules identified on preoperative computed tomography: patterns and clinical significance. Surgery. 2012;151:464−470. doi:10.1016/j.surg.2011.07.032

14. Choi SH, Baek JH, Lee JH, et al. Thyroid nodules with initially non-diagnostic, fine-needle aspiration results: comparison of core-needle biopsy and repeated fine-needle aspiration. Eur Radiol. 2014;24:2819−2826. doi:10.1007/s00330-014-3325-4

15. Yi KS, Kim JH, Na DG, et al. Usefulness of core needle biopsy for thyroid nodules with macrocalcifications: comparison with fine-needle aspiration. Thyroid. 2015;25:657−664. doi:10.1089/thy.2014.0596

16. Na DG, Kim DS, Kim SJ, et al. Thyroid nodules with isolated macrocalcification: malignancy risk and diagnostic efficacy of fine-needle aspiration and core needle biopsy. Ultrasonography. 2016;35:212–219. doi:10.14366/usg.15074

17. Ha EJ, Baek JH, Lee JH, et al. Core needle biopsy can minimise the non-diagnostic results and need for diagnostic surgery in patients with calcified thyroid nodules. Eur Radiol. 2014;24:1403−1409. doi:10.1007/s00330-014-3123-z

18. Zhu D, Chen W, Xiang J, et al. Diagnostic value of CT artifacts for solitary coarse calcifications in thyroid nodules. Int J Clin Exp Med. 2015;8:5800−5805.

19. Zhang LX, Xiang JJ, Wei PY, et al. Diagnostic value of computed tomography (CT) histogram analysis in thyroid benign solitary coarse calcification nodules. J Zhejiang Univ Sci B. 2018;19:211−217. doi:10.1631/jzus.B1700119

20. Han ZJ, Shu YY, Lai XF, et al. Value of computed tomography in determining the nature of papillary thyroid microcarcinomas: evaluation of the computed tomographic characteristics. Clin Imaging. 2013;37:664−668. doi:10.1016/j.clinimag.2012.12.005

21. Han ZJ, Lei ZK, Li MK, et al. Differential diagnosis value of the ultrasound gray scale ratio for papillary thyroid microcarcinomas and micronodular goiters. Quant Imaging Med Surg. 2018;8:507−513. doi:10.21037/qims.2018.06.04

22. Lei ZK, Li MK, Luo DC, et al. The clinical significance of ultrasound grayscale ratio in differentiating markedly hypoechoic and anechoic minimal thyroid nodules. J Cancer Res Ther. 2018;14:1567−1571.

23. Park M, Shin JH, Han BK, et al. Sonography of thyroid nodules with peripheral calcifications. J Clin Ultrasound. 2009;37:324−328. doi:10.1002/jcu.20584

24. Holtz S, Powers WE. Calcification in papillary carcinoma of the thyroid. Am J Roentgenol Radium Ther Nucl Med. 1958;80:997–1000.

25. Yang TT, Huang Y, Jing XQ, et al. CT-detected solitary thyroid calcification: an important imaging feature for papillary carcinoma. Onco Targets Ther. 2016;9:6273−6279. doi:10.2147/OTT.S113369

26. Kim D, Kim DW, Heo YJ, et al. Computed tomography features of benign and malignant calcified thyroid nodules: a single-center study. J Comput Assist Tomogr. 2017;41:937−940. doi:10.1097/RCT.0000000000000618

Creative Commons License © 2020 The Author(s). This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.