Abstract
BACKGROUND:
Fine needle aspiration cytology (FNAC) of the thyroid has been a reliable and cost-effective method for diagnosing thyroid disorders. Since FNAC results are usually operator dependent, there is a compelling need to explore FNAC accuracy among Omanis.
OBJECTIVE:
Describe cytological features of FNAC and assess FNAC accuracy compared to the postsurgical histopathology report.
DESIGN:
Retrospective diagnostic accuracy study
SETTING:
Tertiary care center.
PATIENTS AND METHODS:
Our study included adult Omani adult patients with thyroid nodules who underwent FNAC from 2014 to 2017 and had final pathology results for patients who underwent thyroid surgery. The results were classified according to the UK Royal college of Pathologists ‘Thy’ categories. Accuracy of FNAC was calculated by determining false and true positive and negative results based on histopathology findings.
MAIN OUTCOME MEASURES:
FNAC accuracy (sensitivity and specificity) compared to the postsurgical histopathology.
SAMPLE SIZE:
867 patients with 1359 ultrasound guided FNACs of thyroid nodule; 137 underwent surgery.
RESULTS:
The mean age of the 867 patients was 43.7 (13.3) years, with a median of 42 years, and 87.8% were females. Out of 1359 FNACs, 1001 (73.7%) were benign (Thy2), 119 (8.8%) were atypia of undetermined significance or follicular lesion of undetermined significance (Thy3a), 31 (2.3%) were follicular neoplasm or suspicious for a follicular neoplasm (Thy3f), 52 (3.8%) were suspicious for malignancy (Thy4), 55 (4%) were malignant (Thy5), 101 (7.4%) as Unsatisfactory (Thy1). Only 137 patients underwent thyroid surgery, and the FNAC reports were compared with their final histopathology reports. The sensitivity, specificity and total accuracy of FNAC were 80.2%, 98.9% and 89.9%, respectively. The positive and negative predictive values of FNAC were 98.6% and 84.3%, respectively.
CONCLUSION:
Our study findings confirmed that FNAC of the thyroid is a sensitive, specific, and accurate initial tool for the diagnosis of thyroid lesions. Most of the FNACs were benign with a very low malignancy rate. Due to the minimal chance of false negative results and the slow-growing nature of thyroid malignancy, it is important that patients with benign FNAC should have periodic clinical and radiological follow-up.
LIMITATIONS:
Retrospective design and single-center study, and thyroid nodule size unavailable.
CONFLICT OF INTEREST:
None.
INTRODUCTION
Thyroid nodules are widespread; 4-7% of adults have palpable nodules. Due to the widespread use of ultrasound (US) as a screening tool, many people are incidentally noted to have impalpable nodules.1,2 More than 95% of these thyroid nodules are benign.3 To avoid unwanted invasive thyroid surgeries, it is always better to operate on patients when there is a high suspicion of malignancy. However, clinical presentation alone cannot distinguish benign and malignant lesions.4
Thyroid fine-needle aspiration cytology (FNAC) was first described in 1948.5 FNAC had emerged as a trustworthy, cost-effective, and time-saving tool to diagnose and manage significant thyroid nodules and reduce the rate of unnecessary thyroid surgery, mainly when ultrasound guidance FNA was performed.6 The UK Royal College of Pathologists (RCPath) ‘Thy’ categories for reporting thyroid cytopathology are widely used to guide discussion on further management of thyroid nodules using the Thy classification.7,8 Numerous studies have been published describing FNAC results of thyroid nodules and their accuracy in different parts of the world. Overall, FNAC is reported as being an accurate tool for diagnosing thyroid lesions. A study from France that included 166 patients showed that the diagnostic accuracy was about 89%, with a sensitivity of 68% and specificity of 99.2%.9 Another study from Egypt showed a sensitivity of 92.8% and specificity of 94.2%, with a total accuracy of 93.6%.10
According to the Oman National Cancer Registry (ONCR) Thyroid Cancer, the overall age standardized rate (ASR) from 1996 to 2015 was 5.5/100 000 (7.6 for females and 2.0/100 000 for males),11 While the thyroid cancer ASR was 4.4/100 000 for Saudi Arabia and 5.1/100 000 for the UAE.12,13 Local studies related to thyroid FNAC accuracy are minimal and show conflicting results. One small study conducted in a tertiary care center showed that although FNAC is a sensitive method for diagnosing thyroid lesions, many patients (37.3%) showed inconclusive (unsatisfactory) test results.14 Another local study also showed low FNAC accuracy; however, this study included patients with multinodular goiter only.15 FNAC is usually operator-dependent, and hence, its accuracy may differ in different settings. Therefore, there is a compelling need to explore FNAC accuracy among Omanis. This study aims to evaluate the FNAC accuracy compared to the final histopathology report for Omani adult patients diagnosed with thyroid nodules attending a tertiary care center in Oman. We also describe the cytological features of FNAC outcomes.
PATIENTS AND METHODS
This retrospective study conducted between January 2014 and January 2017 at a tertiary endocrine center in Oman included all patients with single or multiple thyroid nodules diagnosed by physical examination and/or by ultrasound. Demographic data such as age, gender, and the FNAC cytological report were retrieved from the electronic health record. The postsurgical histopathology report of patients who underwent surgery was also retrieved. All FNAC data were used to describe FNAC outcomes; however, only the reports of patients who underwent both FNAC and surgery were used to assess the accuracy.
All FNACs were performed under ultrasound guidance using standard procedures.16 For every nodule, the physician uses three to five separate needles, and the smears were fixed with ether/95% alcohol solution and stained by Papanicolaou's staining. Two expert histopathologists examined each smear. In case of disagreement, a third senior histopathologist was involved to reach a consensus. We classified FNAC results according to the UK Royal College of Pathologists Thy categories system for reporting thyroid cytopathology into six groups; non-diagnostic or unsatisfactory (Thy1), benign (Thy2), atypia of undetermined significance or follicular lesion of undetermined significance (Thy3a), follicular neoplasm or suspicious for a follicular neoplasm (Thy3f), suspicious for malignancy (Thy4), and malignant (Thy5). We considered Thy2 as a benign result and Thy4 and Thy5 as a positive test for malignancy, Thy1 as non-diagnostic, and Thy3a and Thy3f as an intermediate result (Table 1).
Table 1.
The UK Royal College of Pathologists ‘Thy’ categories for reporting thyroid cytopathology.
| Description | Plan of management | |
|---|---|---|
| Thy1 | Non-diagnostic | Repeat FNA or correlate with ultrasound if cystic nodule |
| Thy2 | Benign | Clinical follow up with ultrasound |
| Thy3a | Atypia of undetermined significance or follicular lesion of undetermined significance | Repeat FNA after 3 months |
| Thy3f | Follicular neoplasm or suspicious for follicular neoplasm | Surgical consultation |
| Thy4 | Suspicious of malignancy | Surgical consultation |
| Thy5 | Diagnostic of malignancy | Surgical consultation |
The FNAC results were compared with the post-surgery histopathology. Sensitivity, specificity, diagnostic accuracy, positive predictive value (PPV), and negative predictive value (NPV) of FNAC were calculated. Since it was challenging to include non-diagnostic (Thy1) cases and an intermediate category (Thy3a and Thy3f) under benign or malignant categories, those were excluded from the analysis. IBM SPSS version 23 program (Armonk, New York, United States: IBM Corp) was used for statistical analysis.
RESULTS
During the study period, 867 patients underwent a total of 1359 FNACs, and all the FNACs results were included in the study. Females constituted 87.8%, and the remaining 12.2% were males. The study population's mean (SD) age was 43.7 (13.3) years, with a median of 42 years, and the minimum age being 18 years and the maximum age was 86 years. Out of the total number of FNACs, 1001 (73.7%) were reported as benign (Thy2), 52 (3.8%) as suspicious for malignancy (Thy4), 55 (4%) as malignant (Thy5), 119 (8.8%) as atypia of undetermined significance or follicular lesion of undetermined significance (Thy3a), 31 (2.3%) as follicular neoplasm or suspicious for a follicular neoplasm (Thy3f), 101 (7.4%) as non-diagnostic or unsatisfactory (Thy1).
Out of the total study population (867 patients), 137 patients underwent a thyroid surgery, and their 242 FNAC reports were compared to their postsurgical histopathology report. One-hundred eight patients with nodules in the benign category in FNAC (Thy2) went through surgery due to the large size (>4cm) of the thyroid nodule, of which 91 (84.3%) cases were confirmed benign by histopathologic examination, and the remaining 17 patients were diagnosed as malignant (Table 2). Hence, we had 91 true-negative and 17 false-negative results in the benign category, and the risk of cancer in this group was about 15.7%. Thirty-six patients with an FNA result of Thy3a underwent surgery, out of which 16 cases were malignant. The risk of cancer in this group was 33%. Fifteen cases of Thy3f underwent surgery, of which 3 cases were confirmed to be malignant, with a risk of cancer in this category was about 40%. In the FNAC malignant category (Thy4 and Thy5), 35 cases out of 52 were suspicious of malignancy (Thy4) category and 34 cases out of 55 of the malignant category (Thy5) were operated. The remaining patients either refused surgery or were treated elsewhere. In 34 cases suspicious for malignancy (Thy4), malignancy was confirmed and 1 case was reported as benign in the histopathology results. Hence, the risk of cancer in this category was 91%; however in the malignant (Thy5) category, all cases are confirmed as malignant, and so the risk of cancer was 100%. Out of the total 242 FNACs, only 178 were included for the diagnostic accuracy assessment, excluding patients with undetermined results (Table 3). Thus, FNAC achieved a sensitivity of 80.2% (95% CI 69% - 87%), specificity of 98.9% (95% CI 93% - 99%), and a total accuracy of 89.8% (Table 4).
Table 2.
Detailed fine needle aspiration cytology and histopathological results of patients who underwent surgery (n=137 patients with 242 results).
| FNAC thy code | Histopathology result | Total number | |
|---|---|---|---|
| Benign n (%) | Malignant n (%) | ||
| Thy1 | 12 (85.7) | 2 (14.3) | 14 |
| Thy2 | 91 (84.3) | 17 (15.7) | 108 |
| Thy3a | 16 (44.4) | 20 (55.6) | 36 |
| Thy3f | 12 (80.0) | 3 (20) | 15 |
| Thy4 | 1 (2.9) | 34 (97.1) | 35 |
| Thy5 | 0 (0.0) | 34 (100) | 34 |
| Total | 132 (54.5) | 110 (45.5) | 242 |
Table 3.
Final FNAC versus histopathology results.
| Histopathology | Total | |||
|---|---|---|---|---|
| Benign | Malignant | |||
| FNAC | Benign | 91 | 17 | 108 |
| Malignant | 1 | 69 | 70 | |
| Total | 92 | 86 | 178 | |
Table 4.
Accuracy measures of FNAC compared to histopathology reports (n=178).
| Percentage | 95% CI | |
|---|---|---|
| Sensitivity | 80.2 | 70.3 − 88.0 |
| Specificity | 98.9 | 94.1 − 99.9 |
| Positive predictive value | 98.6 | 90.7 − 99.8 |
| Negative predictive value | 84.3 | 77.8 − 89.1 |
| Positive likelihood ratio | 73.8 | 10.5 − 590.9 |
| Negative likelihood ratio | 0.2 | 0.1 − 0.3 |
| Total accuracy | 89.9 | 84.5 − 93.9 |
DISCUSSION
In this study, the RCPath categorization system was used to study the thyroid FNAc outcomes and its accuracy among Omanis. The results of our study showed that thyroid nodules are more common among females. The study results confirmed that FNAC is a useful diagnostic tool in thyroid nodules work-up with good sensitivity and specificity. Our study showed that almost three-quarters of thyroid nodules are benign, 9% of nodules were Thy3a, 2% were Thy3f, 4% were suspicious for malignancy (Thy4), and 4% were positive for malignancy (Thy5). Our study population's rate of unsatisfactory specimens (Thy1) was relatively low, and the false-negative rate was 19.7%. These results are comparable with other studies.17-19
We noticed that the risk of malignancy of category Thy3a is higher than category Thy3f compared to previous studies. This could be because FNAC is usually unable to distinguish benign lesions like follicular adenomas and hyperplastic follicular nodules from malignant well-differentiated follicular carcinoma.1,18 The introduction of molecular tests in particular analysis for RAS and BRAF gene mutations and RT-PCR for RET/PTC gene rearrangements could differentiate benign from malignant lesions especially in patients who have suspicious features on US as shown in some recent studies. 20,21
The UK Royal College of Pathologists Thy categories for reporting thyroid cytopathology (RCPath) was published in 2009 and reiterated in 2014.22,23 The system currently is of widespread use in the UK and applies to the Thy classification Thy1−Thy5.23 Over the last decades, many other classification schemes for thyroid cytology have been introduced to guide patient management. Examples are the Bethesda system for reporting thyroid cytology (TBSRTC) and the Italian reporting system for thyroid cytology (TIR1-TIR5).24,25 These classification systems are similar but use different terminology.8 All include benign, malignant, suspicious for malignancy, indeterminate, and nondiagnostic categories. However, there are a few differences in the criteria used for classifying FNAC as indeterminate in each classification system. The RCPath Thy3a category is similar to Category III (atypia of undetermined significance (AUS)/follicular lesion of undetermined significance (FLUS) of the Bethesda system. Thy3a differs partially from TIR 3A, which includes only architectural changes without atypias. In contrast, predominantly oncocytic aspirates would be categorized as Thy3f in the RCPath, and as TIR 3B in the Italian system. In addition, Thy2c and Thy1c of the RCPath terminology do not clearly appear in the Bethesda system.
Although the FNAC is undoubtedly a useful diagnostic tool, it does have its limitations mainly due to sampling errors, large nodules, or misinterpretation of the cytological smear that lead to an increase in the false-negative rate (FNR) (patients with benign FNAC but histopathology after surgery shows a malignant lesion). FNRs are a serious concern as there is a possibility of missing malignant lesions, which would go untreated.26 Yet, it is difficult to determine the actual FNR due to only a low proportion (about 10-15%) of patients with benign cytology undergoing surgery.27 The FNR in our study was approximately 15.7%, which is well within the described numbers in the literature, which ranged between 1% and 50%.28-30 Others report FNR from 1.5% to 11.5% (average, <5%).30-32 This variation in FNR is influenced by the number of patients who subsequently have surgery and a histologic review. In most retrospective studies, less than 10% of patients with a benign FNAC subsequently proceeded for thyroid surgery.31,32 Nodules with benign FNA need periodic follow-up with clinical examination and ultrasound to avoid missing malignant lesions in these nodules.29,30
The rate of unsatisfactory FNACs in our study was 7.4%, and the rate reported in the literature ranges between 2% and 20%.18,33 Unsatisfactory FNA sampling could have occurred due to technical issues or may also result from aspiration of calcified nodules, sclerotic areas, cystic nodules, or sold nodules with cystic degeneration. The availability of technically sound expert physicians in FNAC and experienced cytopathologists is crucial to getting an optimal outcome. A repeated FNAC is recommended for unsatisfactory categories and clinically or sonographically worrisome thyroid nodules; repeat FNAC is diagnostic in 50% to 88% of cases.16,34–36
Our study findings indicate that the sensitivity of FNAC is 80%, and specificity is 98% among the Omani population. These results are comparable with other studies, which have reported a range of sensitivity from 65% to 99% and specificity from 72% to 100%.37-41 This wide range of sensitivity and specificity is due to how the authors define the false-positive and false-negative results and categorize suspicious malignant lesions. Some studies include Thy3a and Thy3f in the malignant category, while others categorize them in the negative group, whereas a few studies excluded them from the calculations.37-41 The main limitations of the study were the retrospective design and involvement of only a single center as well as the lack of thyroid nodule sizes.
Table 5.
Comparison of the UK Royal College of Pathologists ‘Thy’ categories for reporting thyroid cytopathology (RCPath) with other internationally used systems.
| RCPath | Bethesda | Italian |
|---|---|---|
| Thy1. Non-diagnostic for cytological diagnosis | I. Non-diagnostic or unsatisfactory | TIR 1. Non-diagnostic |
| Thy1c. Non-diagnostic for cytological diagnosis-cystic lesion | TIR 1c. Non-diagnostic-cystic | |
| Thy2. Non-neoplastic | II. Benign | TIR 2. Non-malignant |
| Thy2c. Non-neoplastic-cystic lesion | ||
| Thy3a. Neoplasm possible-atypia/nondiagnostic | III. AUS/FLUS | TIR 3A. LRIL |
| Thy3f. Neoplasm possible, suggesting follicular neoplasm | IV. Follicular neoplasm or suspicious for a follicular neoplasm | TIR 3B. HRIL |
| Thy4. Suspicious for malignancy | V. Suspicious for malignancy | TIR 4. Suspicious for malignancy |
| Thy5. Malignant | VI. Malignant | TIR 5. Malignant |
AUS, atypia of undetermined significance; FLUS, follicular lesion of undetermined significance; HRIL, high-risk indeterminate lesion; LRIL, low-risk indeterminate lesion; RCPath, Royal College of Pathologists
In conclusion, our study findings confirmed that FNAC of the thyroid is a sensitive, specific, and ac-curate initial tool for the diagnosis of thyroid lesions. Most of the FNACs were benign with a low malignancy rate. Due to the minimal chance of FNR and the slow-growing nature of thyroid malignancy, it is important that patients with benign FNAC should have periodic clinical and radiological follow up.
Funding Statement
Funding: None.
REFERENCES
- 1.Hegedüs L. Clinical practice. The thyroid nodule. N Engl J Med. 2004. Oct 21;351(17):1764–71. doi: 10.1056/NEJM-cp031436. [DOI] [PubMed] [Google Scholar]
- 2.Perros P, Boelaert K, Colley S, Evans C, Evans RM, Gerrard Ba G, et al. ; British Thyroid Association. Guidelines for the management of thyroid cancer. Clin Endocrinol (Oxf). 2014. Jul;81 Suppl 1:1–122. doi: 10.1111/cen.12515. [DOI] [PubMed]
- 3.Durante C, Costante G, Lucisano G, Bruno R, Meringolo D, Paciaroni A, et al. The natural history of benign thyroid nodules. JAMA. 2015. Mar 3;313(9):926–35. doi: 10.1001/jama.2015.0956. [DOI] [PubMed] [Google Scholar]
- 4.Smith TJ, Safaii H, Foster EA, Reinhold RB. Accuracy and cost-effectiveness of fine needle aspiration biopsy. Am J Surg. 1985. Apr;149(4):540–5. doi: 10.1016/s0002-9610(85)80053-2. [DOI] [PubMed] [Google Scholar]
- 5.Diamantis A, Magiorkinis E, Koutselini H. Fine-needle aspiration (FNA) biopsy: historical aspects. Folia Histochem Cytobiol. 2009;47(2):191–7. doi: 10.2478/v10042-009-0027-x. [DOI] [PubMed] [Google Scholar]
- 6.Sakorafas GH. Thyroid nodules; interpretation and importance of fine-needle aspiration (FNA) for the clinician - practical considerations. Surg Oncol. 2010. Dec;19(4):e130–9. doi: 10.1016/j.suronc.2010.06.003. [DOI] [PubMed] [Google Scholar]
- 7.Lobo, C., et al. “The UK Royal College of Pathologists Thyroid Fine-Needle Aspiration Diagnostic Classification Is a Robust Tool for the Clinical Management of Abnormal Thyroid Nodules”. Acta Cytologica 55 (2011): 499–506. [DOI] [PubMed] [Google Scholar]
- 8.Poller DN, Baloch ZW, Fadda G, Johnson SJ, Bongiovanni M, Pontecorvi A, et al. Thyroid FNA: New classifications and new interpretations. Cancer Cytopathol. 2016. Jul;124(7):457–66. doi: 10.1002/cncy.21703. Epub 2016 Feb 23. [DOI] [PubMed] [Google Scholar]
- 9.Prades JM, Querat C, Dumollard JM, Richard C, Gavid M, Timoshenko AA, et al. Thyroid nodule surgery: predictive diagnostic value of fine-needle aspiration cytology and frozen section. Eur Ann Otorhinolaryngol Head Neck Dis. 2013. Sep;130(4):195–9. doi: 10.1016/j.anorl.2012.12.005. Epub 2013 May 20. [DOI] [PubMed] [Google Scholar]
- 10.Sharma C. Diagnostic accuracy of fine needle aspiration cytology of thyroid and evaluation of discordant cases. J Egypt Natl Canc Inst. 2015. Sep;27(3):147–53. doi: 10.1016/j.jnci.2015.06.001. Epub 2015 Jul 14. [DOI] [PubMed] [Google Scholar]
- 11.Al-Lawati NA, Shenoy SM, Al-Bahrani BJ, Al-Lawati JA. Increasing Thyroid Cancer Incidence in Oman: A Joinpoint Trend Analysis. Oman Med J. 2020. Feb 18;35(1):e98. doi: 10.5001/omj.2020.16. PMID: 32095279; PMCID: PMC7029156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Hussain F, Iqbal S, Mehmood A, Bazarbashi S, ElHassan T, Chaudhri N. Incidence of thyroid cancer in the Kingdom of Saudi Arabia, 2000-2010. Hematol Oncol Stem Cell Ther. 2013. Jun;6(2):58–64. doi: 10.1016/j.hemonc.2013.05.004. Epub 2013 Jun 10. PMID: 23756719. [DOI] [PubMed] [Google Scholar]
- 13.Radwan H, Hasan H, Ballout RA, Rizk R. The epidemiology of cancer in the United Arab Emirates: A systematic review. Medicine (Baltimore). 2018. Dec;97(50):e13618. doi: 10.1097/MD.0000000000013618. Erratum in: Medicine (Baltimore). 2019 Jan;98(2):e14220. PMID: 30558043; PMCID: PMC6320101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Alwahaibi N, Alsalami J, Bai UR, Lakhtakia R. Accuracy of fine needle aspiration cytology of thyroid lesion with corresponding histopathology: A single institutional experience. Thyroid Res Pract 2016;13:140–3. doi: 10.4103/0973-0354.193136 [DOI] [Google Scholar]
- 15.Al-Yaarubi S, Farhan H, Al-Futaisi A, Al-Qassabi S, Al-Rasadi K, Al-Riyami S, et al. Accuracy of ultrasound-guided fine-needle aspiration cytology for diagnosis of carcinoma in patients with multinodular goiter. Indian J Endocrinol Metab. 2011. Jul;15(Suppl 2):S132–5. doi: 10.4103/2230-8210.83352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Amrikachi Amrikachi M, Ramzy I, Rubenfeld S, Wheeler TM. Accuracy of fine-needle aspiration of thyroid. Arch Pathol Lab Med. 2001. Apr;125(4):484–8. doi: 10.5858/2001-125-0484-AOFNAO. [DOI] [PubMed] [Google Scholar]
- 17.Piromalli D, Martelli G, Del Prato I, Collini P, Pilotti S. The role of fine needle aspiration in the diagnosis of thyroid nodules: analysis of 795 consecutive cases. J Surg Oncol. 1992. Aug;50(4):247–50. doi: 10.1002/jso.2930500410. [DOI] [PubMed] [Google Scholar]
- 18.Yang J, Schnadig V, Logrono R, Wasserman PG. Fine-needle aspiration of thyroid nodules: a study of 4703 patients with histologic and clinical correlations. Cancer. 2007. Oct 25;111(5):306–15. doi: 10.1002/cncr.22955. [DOI] [PubMed] [Google Scholar]
- 19.Bongiovanni M, Spitale A, Faquin WC, Mazzucchelli L, Baloch ZW. The Bethesda System for Reporting Thyroid Cytopathology: a meta-analysis. Acta Cytol. 2012;56(4):333–9. doi: 10.1159/000339959. Epub 2012 Jul 25. [DOI] [PubMed] [Google Scholar]
- 20.McHenry CR, Phitayakorn R. Follicular adenoma and carcinoma of the thyroid gland. Oncologist. 2011;16(5):585–93. doi: 10.1634/theoncologist.2010-0405. Epub 2011 Apr 11 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Cheung CC, Carydis B, Ezzat S, Bedard YC, Asa SL. Analysis of ret/PTC gene rearrangements refines the fine needle aspiration diagnosis of thyroid cancer. J Clin Endocrinol Metab. 2001. May;86(5):2187–90. doi: 10.1210/jcem.86.5.7504. [DOI] [PubMed] [Google Scholar]
- 22.British Thyroid Association. Guidelines for the management of thyroid cancer (3rd edition). Report of the Thyroid Cancer Guidelines Update Group. London: RCP, 2014. http://www.british-thyroid-association.org/Guidelines/Docs/BTA_DTC_guidlines.pdf (accessed January 2016). [Google Scholar]
- 23.Cross P, Chandra A, Giles T, Johnson S, Kocjan G, Poller Det al. Guidance for the reporting of thyroid cytology (2nd edition). London, UK: The Royal College of Pathologists, 2016 [Google Scholar]
- 24.Baloch ZW, Cibas ES, Clark DP, Layfield LJ, Ljung B-M, Pitman MBet al. The National Cancer Institute Thyroid Fine Needle Aspiration State of the Science Conference: a summation. Cytojournal 2008;5:6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Nardi F, Basolo F, Crescenzi A, Fadda G, Frasoldati A, Orlandi Fet al. Italian consensus for the classification and reporting of thyroid cytology. J Endocrinol Invest 2014;37:593–599. [DOI] [PubMed] [Google Scholar]
- 26.Kantasueb SA, Sukpan KO, Mahanupab PO. The study of thyroid lesions and the correlation between histological and cytological findings. Chiang Mai Med J 2010;49(3):105–10. [Google Scholar]
- 27.Gharib H, Goellner JR. Fine-needle aspiration biopsy of the thyroid: an appraisal. Ann Intern Med. 1993. Feb 15;118(4):282–9. doi: 10.7326/0003-4819-118-4-199302150-00007. [DOI] [PubMed] [Google Scholar]
- 28.Nggada HA, Musa AB, Gali BM, Khalil MI. Fine needle aspiration cytology of thyroid nodule(s); a Nigerian tertiary hospital experience. Internet J Pathol. 2006;5:1 [Google Scholar]
- 29.Radetić M, Kralj Z, Padovan I. Reliability of aspiration biopsy in thyroid nodes: study of 2190 operated patients. Tumori. 1984. Jun 30;70(3):271–6. PMID: 6740771. [DOI] [PubMed] [Google Scholar]
- 30.Hamburger JI. Diagnosis of thyroid nodules by fine-needle biopsy: use and abuse. J Clin Endocrinol Metab. 1994;79:335–9. [DOI] [PubMed] [Google Scholar]
- 31.Giuffrida D, Gharib H. Controversies in the management of cold, hot, and occult thyroid nodules. Am J Med. 1995;99:642-50. [DOI] [PubMed] [Google Scholar]
- 32.Caruso D, Mazzaferri EL. Fine needle aspiration biopsy in the management of thyroid nodules. Endocrinologist. 1991;1:194-202. [Google Scholar]
- 33.Ravetto C, Colombo L, Dottorini ME. The usefulness of fine-needle aspiration in the diagnosis of thyroid carcinoma: a retrospective study in 37,895 patients. Cancer. 2000;90:357–363. [PubMed] [Google Scholar]
- 34.Yassa L, Cibas ES, Benson CB, et al. Long-term assessment of a multidisciplinary approach to thyroid nodule diagnostic evaluation. Cancer. 2007;111:508–516. [DOI] [PubMed] [Google Scholar]
- 35.Goellner JR, Gharib H, Grant CS, et al. Fine-needle aspiration cytology of the thyroid, 1980 to 1986. Acta Cytol. 1987;31:587–590. [PubMed] [Google Scholar]
- 36.Van Hoeven KH, Gupta PK, LiVolsi VA. Value of repeat fine-needle aspiration (FNA) of the thyroid [abstract]. Mod Pathol. 1994;7:43A. [Google Scholar]
- 37.Muratli A, Erdogan N, Sevim S, Unal I, Akyuz S. Diagnostic efficacy and importance of fine-needle aspiration cytology of thyroid nodules. J Cytol. 2014. Apr;31(2):73–8. doi: 10.4103/0970-9371.138666. PMID: 25210233; PMCID: PMC4159900. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Ali Esmaili Heydar, Taghipour Hassan, “Fine-Needle Aspiration in the Diagnosis of Thyroid Diseases: An Appraisal in Our Institution”, International Scholarly Research Notices, vol. 2012, Article ID 912728, 4 pages, 2012. 10.5402/2012/912728 [DOI] [Google Scholar]
- 39.Gunaratne SA, Wijesinghe HKSN, Wijesinghe CJet al. Comparison on fine needle aspiration cytology (FNAC) and thyroid ultrasonography in management of thyroid nodules. Int Clin Pathol J. 2017;5(2):205–209. DOI: 10.15406/icpjl.2017.05.00124 [DOI] [Google Scholar]
- 40.Afroze N, Kayani N, Hasan SH. Role of fine needle aspiration cytology in the diagnosis of palpable thyroid lesions. Indian J Pathol Microbiol. 2002. Jul;45(3):241–6. PMID: 12785159. [PubMed] [Google Scholar]
- 41.Safirullah, N. Mumtaz, and A. Khan, “Role of fine-needle aspiration cytology (FNAC) in the diagnosis of Thyroid swellings”, Journal of PostgraduateMedical Institute, 2004, vol. 18, no. 2, pp. 196–201, [Google Scholar]
