CC BY-NC-ND 4.0 · Int Arch Otorhinolaryngol 2023; 27(01): e138-e142
DOI: 10.1055/s-0042-1748925
Original Research

Risk Factors for Malignancy in Patients with Multinodular Goiter

1   Faculdade de Ciências da Saúde, Universidade Metropolitana de Santos, Santos, SP, Brasil
,
2   Surgery Department, Faculdade de Medicina da USP, São Paulo, SP, Brasil
,
2   Surgery Department, Faculdade de Medicina da USP, São Paulo, SP, Brasil
3   Discipline of Scientific Methodology, Universidade Metropolitana de Santos, Santos, SP, Brasil
› Author Affiliations
 

Abstract

Introduction The identification of thyroid cancer may be conducted through clinical detection, imaging method, and histopathological examination. Both solitary nodules and multinodular goiter are associated with malignancy.

Objective To assess the risk factors for malignancy among patients with multinodular goiter submitted to total thyroidectomy.

Methods A series of 712 consecutive patients, submitted to total thyroidectomy between 2005 and 2016 with multinodular goiter regarding clinical, ultrasound, and pathological variables, was retrospectively evaluated.

Results There were 408 cases of papillary carcinoma (57.3%), with the remaining being benign. Gender had no statistical significance (p = 0.169) for malignancy, unlike the Bethesda index, higher age group (p = 0.005), shorter clinical history time (p = 0.036), smaller number of nodules (p < 0.0001), and smaller nodule size (p < 0.0001), which were related to malignancy.

Conclusion The Bethesda index, older age group, shorter clinical history, smaller number of nodules, and smaller size of nodule were related to the diagnosis of papillary carcinoma.


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Introduction

Thyroid nodules are a common entity in the daily practice. They are observed in ∼ 8% of the adult population and are more frequent in women.[1] Malignant neoplasms represent ∼ 1% of all malignant tumors and are the most common endocrine neoplasms. Thyroid nodules present a malignancy prevalence of 5 to 15%.[2] The overall incidence of papillary carcinoma is the highest among thyroid incidentalomas. The incidence is higher when, in the context of goiter, there is an association with follicular adenoma and the total thyroidectomy must be considered as the treatment of choice, being currently practiced by most treatment centers.[3]

The identification of thyroid cancer can be classified into three broad situations: cancer detected clinically; detected by imaging method (without clinical suspicion); and detected by histopathological examination (without clinical suspicion and via imaging method).[4] Incidental carcinoma is, after surgical resection of the thyroid gland by benign pathology, the most frequent event.[5] In thyroidectomy specimens, the prevalence of incidentaloma reaches 40%.[6] Regarding the association of papillary thyroid carcinoma with chronic thyroiditis, thyroiditis was found in 26.8% of patients treated for the tumor, however, with no connection to cancer size.[7]

Due to advances in imaging techniques, the chances of detecting thyroid nodules have increased dramatically. Thus, the incidence of thyroid cancer is increasing. Patients with palpable thyroid nodules have a 20 to 57% chance of finding additional nodules on ultrasound examination.[8] Both solitary nodules and multinodular goiter are associated with malignancy. Solitary nodules are generally considered to have a higher risk of malignancy than multinodular goiter,[2] [9] although some data suggest that the risk is equal.[10] [11] A preoperative assessment of thyroid nodules, to stratify them into benign and malignant, is important to avoid unnecessary surgeries and related problems.[9] [12] The surgical approach is indicated for suspicion of malignancy, in case of indeterminate cytopathology and high risk context, larger nodules (mainly with compressive symptoms), and in selected cases of thyrotoxicosis.[13]

Some risk factors for malignancy in thyroid nodules related to inflammation have been added. Erythrocyte distribution width (RDW), an inflammatory marker, was retrospectively studied in the preoperative hemogram of patients who underwent thyroidectomy, and it was significantly higher in those with cancer in comparison with those with benign nodules and in the control group.[14] Similarly, mean platelet volume (MPV) was retrospectively analyzed in hemograms, being significantly higher in the malignant nodule group than in the benign nodule group.[15] Neutrophil to lymphocyte ratio (NLR) was significantly higher in the malignant nodule group than in both the benign nodule and control groups, as well.[16] Thus, such factors should alert for the possibility of malignancy. Furthermore, their cost is low.

The objective is to assess patients with multinodular goiter submitted to total thyroidectomy for the presence of malignancy regarding the epidemiological, clinical, and pathological aspects.


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Methods

This study was approved by the institutional review board under the number 3.154.631.

A total of 712 consecutive patients, who underwent total thyroidectomy between 2005 and 2016, were retrospectively assessed. The inclusion criterion was patients presenting more than one nodule in preoperative radiological images, who had not previously been submitted to surgery on the gland. Our indications for surgical approach were suspicion (or confirmation) of malignancy and large goiters with compressive signs; aesthetic indication was not considered. Patients presenting malignancy findings of other cancers different from the papillary carcinoma on the histopathological examination and those with suppressed thyroid-stimulating hormone (TSH) were excluded.

In the surgical routine, the parathyroid glands and recurrent laryngeal nerves were identified, and the specimens were sent to the pathologist for frozen intraoperative examination. A drain was placed systematically on the immediate postoperative day. All patients were discharged on the first postoperative day, with the prescription of levothyroxine adjusted according to the patient's weight.

The following items were assessed: age (in years); gender (male or female); time of clinical history (in months); the number of nodules detected on ultrasound; the size in millimeters of the dominant nodule (largest on the largest axis); and fine-needle aspiration biopsy (FNAB) result (all aspiration punctures were performed under ultrasound guidance and their results were categorized according to the Bethesda classification). Nodules with higher and intermediate risks of malignancy,[17] and/or all nodules presenting 2 cm or more at its largest axis, were elected to be biopsied. When more than one FNAB was performed on the same gland, we considered, for purposes of eventual surgical indication, the one with the highest Bethesda index.

The values obtained with the analysis of quantitative variables were organized and described by means, median, standard deviation, minimum, and maximum. For categorized variables, absolute and relative frequencies were used. The distributions were defined as parametric by the Kolmogorov-Smirnov test. For the comparison of quantitative variables between two sample populations, the Student t-test was used, and for the frequency comparisons, the chi-squared test was used. In all analyses, the statistical program IBM SPSS Statistics for Windows, version 24.0 (IBM Corp., Armonk, NY, USA) was used, and a statistical significance level of 5% (p < 0.05) was adopted.


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Results

From the 712 patients analyzed, 623 (87.5%) were female, most of whom (329–46.2%) presented two nodules on ultrasound. The non-absolute majority (275–38.6%) of the patients had a Bethesda III result on cytopathological examination. On histopathological examination, a total of 408 cases revealed papillary carcinoma (57.3%), with the remaining being benign (adenomatous goiter, follicular adenoma, and/or chronic lymphocytic thyroiditis), as shown in [Table 1].

Table 1

Epidemiological, clinical, and pathological variables

 Variable

 Aspect

 n

 %

 Gender

 Male

 89

 12.5%

 Female

 623

 87.5%

 Number of nodules

 2

 329

 46.2%

 3

 141

 18.4%

 4

 93

 13.1%

 5

 54

 7.6%

 6

 35

 4.9%

 7

 22

 3.1%

 8

 14

 2%

 9

 8

 1.1%

 11

 3

 0.4%

 13

 2

 0.3%

 15

 1

 0.1%

 FNAB (Bethesda)

 II

 213

 30%

 III

 275

 38.6%

 IV

 100

 14%

 V

 78

 10.9%

 VI

 46

 6.3%

 Histopathological

 Benign

 304

 42.7%

 Papillary carcinoma

 408

 57.3%

Abbreviation: FNAB, fine-needle aspiration biopsy.


When relating the variables studied to the final finding of malignancy, the gender (male or female) was not statistically significant (p = 0.169). High Bethesda classes were highly related to malignancy, especially V and VI, as shown in [Table 2]. Considering the unexpected finding of malignancy among Bethesda II cases, we can consider that 38 of 213 cases (17.8%) can be stratified as incidental papillary carcinoma. Thus, since the total series gathered 712 patients, there were 5.3% of incidental tumors. On the other hand, among those 38 cases of papillary carcinoma with previous Bethesda II, 19 nodules' sizes varied from 1 to 9 mm. They could be classified as incidentaloma due to the size criterion.

Table 2

Correlation of gender and Bethesda index with malignancy

 Variable

 Aspect

 Benign

 Papillary carcinoma

 p*

 Gender

 Male

 45

 44

 0.169

 Female

 363

 260

 Bethesda

 II

 175

 38

 < 0.0001

 III

 168

 107

 IV

 54

 46

 V

 9

 69

 VI

 3

 43

* Chi-squared test.


Other aspects had significance; this is to say, the cases of papillary carcinoma presented higher age range (p = 0.005), shorter time of clinical history until the moment of surgical intervention (p = 0.036), smaller number of nodules on ultrasound (p < 0.0001), and smaller size of the largest measurement axis (p < 0.0001), as shown in [Table 3].

Table 3

Correlation of clinical aspects with malignancy

 Variable

 Histopathological*

 Average

 Standard deviation

 Mean standard error

 p**

 Age

 Benign

 52.77

 13.394

 0.663

 0.005

 Papillary ca

 49.82

 14.318

 0.821

 History time (months)

 Benign

 33.05

 46.213

 2.288

 0.036

 Papillary ca

 25.37

 50.760

 2.921

 Number of nodules on US

 Benign

 3.35

 2.101

 0.104

 < 0.0001

 Papillary ca

 2.71

 1.927

 0.111

 Highest measurement (mm)

 benign

 26.46

 13.141

 0.651

 < 0.0001

 Papillary ca

 14.72

 13.834

 0.795

Abbreviation: US, ultrasound.


* benign = 408; papillary carcinoma = 304.


** Student t-test.



#

Discussion

The papillary thyroid carcinoma is the most prevalent and the one presenting the best prognosis among all thyroid malignancies.[2] The reported overall incidence of thyroid carcinoma is only ∼ 5%. Some studies have suggested that the incidence of malignancy may be higher for solitary nodules than for multiple nodules. Our study addressed patients submitted to multinodular goiter thyroidectomy. In a study of 265 single-node operated patients, male gender, microcalcification, and lymphadenopathy were independent risk factors for predicting malignancy in patients with solitary thyroid nodule.[9]

Over the past 30 years, there has been an increase in the overall incidence of thyroid cancer.[4] The incidence rate of papillary carcinoma has increased more than any other malignant neoplasm.[10] Thus, it is important to recognize risk factors for malignancy in the context of nodular thyroid disease. Our overall occurrence of cancer was high (57.3%), compared with other similar studies.[11] [12]

We did not find differences of malignancy risk regarding gender. This is aligned with other findings in the literature that did not show statistical difference;[4] [7] however, there are studies in which the incidence of malignancy in male patients is higher than that found in women,[2] [9] as shown in [Table 2]. In this study, an association of malignancy was observed in older patients, which is in accordance with the literature, with a higher prevalence in individuals around 50 to 60 years of age or older.[7] [9]

The same situation was observed regarding the number of nodules, because as the number increased, the frequency of cancer decreased, also in accordance with the literature[2] [6] [9], as shown in [Table 3]. However, regarding the size of the nodule, the findings differed from the literature. There was no significant relationship between nodule size and the likelihood of papillary carcinoma.[2] In our results, we observed that the average size of the benign lesion was bigger than the that of malignant ones.

Regarding the time of clinical history, this was higher among patients with goiter, compared with those with papillary carcinoma, as shown in [Table 3].

The value of ultrasound and fine needle aspiration biopsy (FNAB) as a diagnostic tool for thyroid cancer in patients with endemic multinodular goiter is limited, mainly due to the high number of nodules and to the fact that thyroidectomy indications are currently not well-defined.[5] Although ultrasound findings suggesting malignancy include dominant hypoechoic nodules, thick or irregular halo, microcalcifications, and increased intranodular flow, the poor ultrasound accuracy disqualifies the differentiation between benign and cancerous lesions.[18] The indications for thyroid ultrasonography should be palpable goiter and nodules. Specialists with expertise in thyroid sonography are recommended. Thus, since the detection of early thyroid cancer does not improve survival rates, routine ultrasonographic screening should not be done, with the exception of high-risk patients.[13] In patients with diffuse multinodular disease, FNAB has certain limitations. Usually, nodules with less than 1 cm of diameter are usually not biopsied, and although ultrasound may guide FNAB for radiographically suspected lesions, malignancy may exist in alternate positions.[5] Since, by definition, a multinodular goiter contains more than one nodule, the clinician faces the difficult decision to select which nodule(s) will be used in the biopsy. One approach adopted was to perform a biopsy only in the nodules that are dominant (by size).[19] In our study, the FNAB was performed on dominant nodules or on those with suspicious ultrasound morphology, and the Bethesda index of cytopathological examination showed statistical significance with the finding of malignancy.Each nodule in the contexto of multinodular goiter should be followed up individually.


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Conclusion

The factors related to the diagnosis of papillary carcinoma were the Bethesda index, older age group, shorter clinical history, smaller number of nodules, and smaller nodule size.


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Conflict of Interests

The authors have no conflict of interests to declare.

  • References

  • 1 Li H, Li J. Thyroid disorders in women. Minerva Med 2015; 106 (02) 109-114
  • 2 Frates MC, Benson CB, Doubilet PM. et al. Prevalence and distribution of carcinoma in patients with solitary and multiple thyroid nodules on sonography. J Clin Endocrinol Metab 2006; 91 (09) 3411-3417
  • 3 Rahman MM, Abdullah US, Joarder AI, Das C, Debnath BC, Sah R. Incidental thyroid carcinoma in patients treated surgically for presumably benign thyroid disease. Mymensingh Med J 2017; 26 (03) 569-573
  • 4 Fama F, Sindoni A, Cicciu M. et al. Preoperatively undiagnosed papillary thyroid carcinoma in patients thyroidectomized for benign multinodular goiter. Arch Endocrinol Metab 2018; 62 (02) 139-148
  • 5 Lasithiotakis K, Grisbolaki E, Koutsomanolis D. et al. Indications for surgery and significance of unrecognized cancer in endemic multinodular goiter. World J Surg 2012; 36 (06) 1286-1292
  • 6 Siassakos D, Gourgiotis S, Moustafellos P, Dimopoulos N, Hadjiyannakis E. Thyroid microcarcinoma during thyroidectomy. Singapore Med J 2008; 49 (01) 23-25
  • 7 Campos LA, Picado SM, Guimarães AV, Ribeiro DA, Dedivitis RA. Thyroid papillary carcinoma associated to Hashimoto's thyroiditis. Rev Bras Otorrinolaringol (Engl Ed) 2012; 78 (06) 77-80
  • 8 Brander A, Viikinkoski P, Tuuhea J, Voutilainen L, Kivisaari L. Clinical versus ultrasound examination of the thyroid gland in common clinical practice. J Clin Ultrasound 1992; 20 (01) 37-42
  • 9 Tai JD, Yang JL, Wu SC, Wang BW, Chang CJ. Risk factors for malignancy in patients with solitary thyroid nodules and their impact on the management. J Cancer Res Ther 2012; 8 (03) 379-383
  • 10 Boucek J, Kastner J, Skrivan J. et al. Occult thyroid carcinoma. Acta Otorhinolaryngol Ital 2009; 29 (06) 296-304
  • 11 Ajarma KY, Al-Faouri AF, Al Ruhaibeh MK. et al. The risk of thyroid carcinoma in multinodular goiter compared to solitary thyroid nodules: A retrospective analysis of 600 patients. Med J Armed Forces India 2020; 76 (01) 23-29
  • 12 Rabal Fueyo A, Vilanova Serra M, Lerma Puertas E. et al. Diagnostic accuracy of ultrasound and fine-needle aspiration in the study of thyroid nodule and multinodular goitre. Endocrinol Diabetes Metab 2018; 1 (03) e00024
  • 13 Wong R, Farrell SG, Grossmann M. Thyroid nodules: diagnosis and management. Med J Aust 2018; 209 (02) 92-98
  • 14 Aktas G, Sit M, Karagoz I. et al. Could red cell distribution width be a marker of thyroid cancer?. J Coll Physicians Surg Pak 2017; 27 (09) 556-558
  • 15 Sit M, Aktas G, Ozer B. et al. Mean platelet volume: An overlooked herald of malignant thyroid nodules. Acta Clin Croat 2019; 58 (03) 417-420
  • 16 Sit M, Aktas G, Erkol H, Yaman S, Keyif F, Savli H. Neutrophil to lymphocyte ratio is useful in differentiation of malign and benign thyroid nodules. P R Health Sci J 2019; 38 (01) 60-63
  • 17 Gharib H, Papini E, Garber JR. et al; AACE/ACE/AME Task Force on Thyroid Nodules. American Association of Clinical Endocrinologists, American College of Endocrinology, and Associazione Medici Endocrinologi Medical Guidelines for Clinical Practice for the Diagnosis and Management of Thyroid Nodules–2016 Update. Endocr Pract 2016; 22 (05) 622-639
  • 18 Moon HJ, Kwak JY, Kim EK. et al. The combined role of ultrasound and frozen section in surgical management of thyroid nodules read as suspicious for papillary thyroid carcinoma on fine needle aspiration biopsy: a retrospective study. World J Surg 2009; 33 (05) 950-957
  • 19 Tollin SR, Mery GM, Jelveh N. et al. The use of fine-needle aspiration biopsy under ultrasound guidance to assess the risk of malignancy in patients with a multinodular goiter. Thyroid 2000; 10 (03) 235-241

Address for correspondence

Guilherme Arruda Fernandes, MD
Faculdade de Ciências da Saúde, Universidade Metropolitana de Santos
Av. Conselheiro Nébias, 444, 16° andar – Encruzilhada, Santos, SP 11045-000
Brazil   

Publication History

Received: 24 May 2020

Accepted: 21 March 2022

Article published online:
17 June 2022

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  • References

  • 1 Li H, Li J. Thyroid disorders in women. Minerva Med 2015; 106 (02) 109-114
  • 2 Frates MC, Benson CB, Doubilet PM. et al. Prevalence and distribution of carcinoma in patients with solitary and multiple thyroid nodules on sonography. J Clin Endocrinol Metab 2006; 91 (09) 3411-3417
  • 3 Rahman MM, Abdullah US, Joarder AI, Das C, Debnath BC, Sah R. Incidental thyroid carcinoma in patients treated surgically for presumably benign thyroid disease. Mymensingh Med J 2017; 26 (03) 569-573
  • 4 Fama F, Sindoni A, Cicciu M. et al. Preoperatively undiagnosed papillary thyroid carcinoma in patients thyroidectomized for benign multinodular goiter. Arch Endocrinol Metab 2018; 62 (02) 139-148
  • 5 Lasithiotakis K, Grisbolaki E, Koutsomanolis D. et al. Indications for surgery and significance of unrecognized cancer in endemic multinodular goiter. World J Surg 2012; 36 (06) 1286-1292
  • 6 Siassakos D, Gourgiotis S, Moustafellos P, Dimopoulos N, Hadjiyannakis E. Thyroid microcarcinoma during thyroidectomy. Singapore Med J 2008; 49 (01) 23-25
  • 7 Campos LA, Picado SM, Guimarães AV, Ribeiro DA, Dedivitis RA. Thyroid papillary carcinoma associated to Hashimoto's thyroiditis. Rev Bras Otorrinolaringol (Engl Ed) 2012; 78 (06) 77-80
  • 8 Brander A, Viikinkoski P, Tuuhea J, Voutilainen L, Kivisaari L. Clinical versus ultrasound examination of the thyroid gland in common clinical practice. J Clin Ultrasound 1992; 20 (01) 37-42
  • 9 Tai JD, Yang JL, Wu SC, Wang BW, Chang CJ. Risk factors for malignancy in patients with solitary thyroid nodules and their impact on the management. J Cancer Res Ther 2012; 8 (03) 379-383
  • 10 Boucek J, Kastner J, Skrivan J. et al. Occult thyroid carcinoma. Acta Otorhinolaryngol Ital 2009; 29 (06) 296-304
  • 11 Ajarma KY, Al-Faouri AF, Al Ruhaibeh MK. et al. The risk of thyroid carcinoma in multinodular goiter compared to solitary thyroid nodules: A retrospective analysis of 600 patients. Med J Armed Forces India 2020; 76 (01) 23-29
  • 12 Rabal Fueyo A, Vilanova Serra M, Lerma Puertas E. et al. Diagnostic accuracy of ultrasound and fine-needle aspiration in the study of thyroid nodule and multinodular goitre. Endocrinol Diabetes Metab 2018; 1 (03) e00024
  • 13 Wong R, Farrell SG, Grossmann M. Thyroid nodules: diagnosis and management. Med J Aust 2018; 209 (02) 92-98
  • 14 Aktas G, Sit M, Karagoz I. et al. Could red cell distribution width be a marker of thyroid cancer?. J Coll Physicians Surg Pak 2017; 27 (09) 556-558
  • 15 Sit M, Aktas G, Ozer B. et al. Mean platelet volume: An overlooked herald of malignant thyroid nodules. Acta Clin Croat 2019; 58 (03) 417-420
  • 16 Sit M, Aktas G, Erkol H, Yaman S, Keyif F, Savli H. Neutrophil to lymphocyte ratio is useful in differentiation of malign and benign thyroid nodules. P R Health Sci J 2019; 38 (01) 60-63
  • 17 Gharib H, Papini E, Garber JR. et al; AACE/ACE/AME Task Force on Thyroid Nodules. American Association of Clinical Endocrinologists, American College of Endocrinology, and Associazione Medici Endocrinologi Medical Guidelines for Clinical Practice for the Diagnosis and Management of Thyroid Nodules–2016 Update. Endocr Pract 2016; 22 (05) 622-639
  • 18 Moon HJ, Kwak JY, Kim EK. et al. The combined role of ultrasound and frozen section in surgical management of thyroid nodules read as suspicious for papillary thyroid carcinoma on fine needle aspiration biopsy: a retrospective study. World J Surg 2009; 33 (05) 950-957
  • 19 Tollin SR, Mery GM, Jelveh N. et al. The use of fine-needle aspiration biopsy under ultrasound guidance to assess the risk of malignancy in patients with a multinodular goiter. Thyroid 2000; 10 (03) 235-241