Get Permission Singh, Prakash, Amita K, Abhishek MG, and Shankar S: Efficacy of AGNOR staining on FNAC smears in non-neoplastic and neoplastic thyroid lesions with special emphasis on distinguishing benign from the malignant


Introduction

Thyroid gland is affected by a vast array of developmental, inflammatory, hyperplastic and neoplastic disorders. The prevalence of palpable thyroid nodule is 4 to 7% in the adult population and 0.2 to 2% in children.1 Approximately 2-4 / 1,00,000 people per year are identified with a malignant thyroid lesion, accounting for 1% of all cancers and 0.5% of all cancer deaths.2 It is important to rule out neoplasms in an enlarged thyroid gland as it necessitates surgical intervention. As for most lesions, distinction between benign from a malignant thyroid nodule is vital in preventing misdiagnosis with early diagnosis and prompt treatment definitely leading to a better outcome.

It has already been proven that FNAC of the thyroid gland is safe, minimally invasive, sensitive, specific, accurate, economically viable and an easily performed OPD procedure3 and along with molecular biomarkers have shown great promise in detecting malignancy.4 But FNAC has certain limitations which include false negative and false positive results and results which fall into the indeterminate or grey zone category where the lesions are not obviously benign or malignant.5

Usefulness of silver staining technique for nucleolar organizing region (AgNOR) is well known and has been applied to a variety of neoplastic lesions or pathological material in order to distinguish benign from malignant.6 In this study, AgNOR staining is used along with cytomorphological features in FNAC of the thyroid lesion to differentiate benign from malignant neoplasm and thus improving its diagnostic accuracy

Materials and Methods

This was a prospective time bound study done in the department of pathology, Adichunchanagiri Institute of medical Sciences, BG Nagara, Karnataka over a duration of one and half years from November 2016 to April 2018. Ethical committee approval was obtained from the institutional review board and institutional ethical committee. All the cases presenting to cytology clinic with thyroid lesions for fine needle aspiration cytology (FNAC) were included in the study. Patients from whom inadequate material was aspirated from the thyroid lesion and non-cooperative cases in whom FNAC was not performed were excluded from the study. Demographic data and radiologic findings when available were recorded. Thorough local examination for the location, size, nodularity, and consistency was done and the findings were recorded. FNAC was done by the trained cytopathologist using 23 G needle. A maximum of two passes was performed. In case of large swellings aspiration was done from different areas to minimize sampling error. From aspirated material, 4–6 smears were made, out of them 2–4 smears were immediately fixed in 95% ethyl alcohol for haematoxylin & eosin (H & E) stain and Papanicolaou stain and rest of the 2 smears were air dried, one for Giemsa stain and other subsequently fixed in 95% alcohol for AgNOR stain. Cytological diagnosis was done from Pap-stained, H&E stained and Giemsa stained smears and analysis of AgNORs done from AgNOR-stained smear to differentiate benign from malignant lesions.

Silver stained NORs which appeared as black dots were counted two different times by a single observer at a magnification of 100X oil immersion lens. 100 representative nuclei of thyroid follicular cells were selected. A mean was calculated , which represented mean AgNOR count. Quantifications were always performed in well-preserved cells, excluding areas of staining artifacts or overlapped cells. In cases where only two smears were made. It was stained with H & E and Giemsa stain. After FNAC diagnosis was made. H&E stained slides were destained with solution of acid-alcohol and were stained with AgNOR stain which gave similar results.

Statistical analysis

In this Prospective study, cytological diagnosis was obtained by correlation of clinical history, clinical diagnosis, radiological findings, adequacy of smear, predominant patterns and individual cell cytomorphology. Histopathological correlation was done wherever possible. AgNOR count was done in all the cases.

Tabulated data was analyzed systematically by the use of appropriate statistical methods and SSPS software and results were obtained. Data were expressed as mean values and percentage Comparison between groups were done by unpaired t test and one way ANOVA test. Sensitivity, specificity, standard deviation and range were analyzed whenever required. A p value of less than 0.05 was considered to be statistically significant.

Results

Demography

A total of 150 cases were who underwent thyroid gland FNAC were included in the study group. The mean age of patient was 39.6 years, the youngest patient was 8 years old and oldest was 70 years old. Females were more frequently affected with male to female ratio being 1:15.6.

Overall mean AgNOR of all the 150 cases of thyroid lesions was 2.55 (SD±1.47, CI 95%) and with range of 0-10.2. Hashimoto’s thyroiditis has maximum of 56 cases followed by 40 cases of colloid goiter and 8 cases of adenomatous goiter. There were 2 cases of Dequervain’s thyroiditis with mean AgNORcount of 2.70 (SD±0.42, CI 95%) and range of 2.4-3. There were two cases of hurtle cell neoplasm with mean AgNOR count of 3.5 (SD±0.14, CI 95%) in the range of 3.4-3.6. Only one case of Anaplastic carcinoma was there with AgNOR count of 4.80. Single case of metastatic deposits of squamous cell carcinoma was there with AgNOR count of 10.2. There was statistically significant difference in the mean AgNOR score among various thyroid lesions (p=0.000). The distribution of total 150 cases along with their mean AgNOR score is shown in Table 1.

Total number of benign thyroid cases were 131. Overall mean AgNOR count of benign thyroid lesions was found to be 2.20 (SD±1.06, CI 95%) with a range of 0-3.8. Total number of malignant thyroid cases were 19. Overall mean AgNOR count of malignant thyroid lesions was found to be 4.92 (SD±1.71, CI 95%) with a range of 2.6-10.2. Out of 150 cases, histopathological diagnosis was available in 18 cases. There were 9 cases of papillary carcinoma thyroid, three cases of Non Invasive Follicular Thyroid Neoplasm with Papillary like nuclear features (NIFTP), one case of hurtle cell adenoma, two cases of follicular adenoma, one case of follicular carcinoma, and one case of multinodular goiter and one case of Sclerosing variant of HT. Overall mean AgNOR count of histopathological diagnosis was 2.55 (SD±1.47, CI 95%) and range was from 0-10.2. Follicular adenoma had mean AgNOR count of 3.05 (SD±0.49, CI 95%) and range was 2.7-3.4. Single case of follicular carcinoma had mean AgNOR count of 4.6. Single case of Hurthle cell adenoma had mean AgNOR count of 3.6. There were three cases of NIFTP, which had mean AgNOR count of 3.63 (SD±0.32, CI 95%) and range was 3.4-4. Correlation between AgNOR count and histopathological diagnosis is shown in Table 2.

Figure 1

A: FNAC showing benign thyroid follicular cells with AgNOR dots in colloid goitre. Without counter stain(Methyl Green) (AgNOR, x400), B: FNAC showing cluster of benign thyroid follicular cells with AgNOR dots in Hashimoto’s Thyroiditis. Without counter stain(Methyl green)(AgNOR, x400), C: FNAC showing clusters of benign thyroid follicular cells in Hyperplastic Goitre.(AgNOR, x400), D: FNAC showing clusters of benign thyroid follicular cells in Hyperplastic Goitre with AgNOR dots.(AgNOR, x1000)

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Figure 2

A: FNAC showing thyroid follicular cells arranged in microfollicles in Follicular Neoplasm. (AgNOR, x40), B: FNAC showing thyroid follicular cells in Follicular Neoplasm with AgNOR dots. (AgNOR, x1000), C: FNAC showing thyroid follicular cells arranged in sheets in Papillary carcinoma thyroid. Without counterstain (Methyl green)(AgNOR, x40), D: FNAC showing cluster of thyroid follicular cells in Papillary carcinoma thyroid with AgNOR dots (AgNOR,x1000)

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Table 1

Mean value of AgNOR count with SD for different thyroid lesion with P value between them

N Mean Std. Deviation Std. Error 95% Confidence Interval for Mean Minimum Maximum
Lower Bound Upper Bound
Acute Thyroiditis 1 2.800 2.8 2.8
Adenomatous Goitre 8 2.875 .2375 .0840 2.676 3.074 2.4 3.2
Anaplastic Carcinoma 1 4.800 4.8 4.8
Colloid Goitre 40 1.500 1.2961 .2049 1.085 1.915 0.0 3.4
Dequervain's thyroiditis 2 2.700 .4243 .3000 -1.112 6.512 2.4 3.0
Follicular Neoplasm 3 3.567 .9609 .5548 1.180 5.954 2.7 4.6
HT 56 2.416 .8746 .1169 2.182 2.650 0.0 3.8
Hurtle Cell Neoplasm 2 3.500 .1414 .1000 2.229 4.771 3.4 3.6
Hyperplastic goitre 20 2.500 .5487 .1227 2.243 2.757 1.8 3.8
Lymphocytic thyroiditis 1 2.000 2.0 2.0
Metastatic deposits of SCC 1 10.200 10.2 10.2
papillary carcinoma thyroid. 15 4.733 1.1800 .3047 4.080 5.387 3.2 7.1
Total 150 2.548 1.4693 .1200 2.311 2.785 0.0 10.2
Table 2

Correlation between AgNOR count and histopathological diagnosis

Histopathological diagnosis N Mean Std. Deviation Std. Error 95% Confidence Interval for Mean Minimum Maximum
Lower Bound Upper Bound
Follicular Adenoma 2 3.050 .4950 .3500 -1.397 7.497 2.7 3.4
Follicular carcinoma 1 4.600 4.6 4.6
Hurtle cell Adenoma 1 3.600 3.6 3.6
MNG 1 2.400 2.4 2.4
NIFTP 3 3.633 .3215 .1856 2.835 4.432 3.4 4.0
Not done 132 2.298 1.3069 .1138 2.073 2.523 0.0 10.2
PTC 8 5.275 1.1119 .3931 4.345 6.205 4.2 7.1
PTC- mixed follicular and papillary variant 1 5.900 5.9 5.9
Sclerosing variant of HT 1 3.200 3.2 3.2
Total 150 2.548 1.4693 .1200 2.311 2.785 0.0 10.2
Table 3

Comparision ofMean AgNOR Scores and Standard Deviation (SD) in Benign Thyroid lesions

Author(s) Year Total number of Thyroid cases Number of benign thyroid cases Mean AgNOR score SD
Varghese et al 8 2017 50 28 2.04 1.157
Hossain et al 10 2012 157 148 1.91 0.36
Eroz et al 9 2011 56 30 2.0 0.5
Asotra et al 6 2008 140 100 2.94 0.085
Mehrotra et al 7 1998 140 62 2.28 0.88
Present study 2018 150 131 2.20 1.06
Table 4

   Comparision of Mean AgNOR Scores and Standard Deviation (SD) in Malignant Thyroid lesions.

Author(s) Year Total number of thyroid cases Number of malignant thyroid cases Mean AgNOR score SD
Varghese et al 8 2017 50 22 7.46 3.329
Hossain et al 10 2012 157 9 2.84 0.32
Eroz et al 9 2011 56 26 4.6 1.2
Asotra et al 6 2008 140 40 4.27 0.41
Mehrotra et al 7 1998 140 78 3.49 0.62
Present study 2018 150 19 4.92 1.71
Table 5

   Comparision of Mean AgNOR Scores and Standard Deviation (SD) in different thyroid lesions.

Authors Year Colloid Goitre Hashimoto’s Thyroiditis Hyperplastic Goitre Follicular Neoplasm PTC
Varghese et al 8 2017 1.16±0.167 1.194±0.407 1.52±0.46 5.03±0.251 7.65±3.18
Chalsie et al 11 2013 2.64 ± 0.63 2.10±0.36 3.04±0.8 4.10±1.13 5.40±0.86
Asotra et al 6 2008 2.94±0.85 2.76±0.082 2.82±0.088 3.15±0.80 5.08±1.11
Present Study 2018 1.73±1.29 2.42±0.874 2.50±0.548 3.567±0.96 4.73±1.18

Discussion/Conclusion

Thyroid disease is a common clinical problem. It is important to distinguish non-neoplastic and neoplastic thyroid lesions. FNAC is safest and cost effective method of preoperative diagnosis of thyroid lesions. The majority of thyroid nodules have a characteristic cytological pattern, allowing specific diagnosis.12 But, FNAC has certain limitations, especially in case of thyroid neoplasm.

AgNOR analysis is a method for routine assessments of cell proliferation rapidity.13, 14, 15

However, AgNOR measurement is affected by several factors such as temperature and method of counting. Other ancillary techniques such as enzyme techniques, DNA measurements, immunocytochemistry and morphometric studies have been used with varying degree of success in differentiating benign and malignant thyroid neoplasm. AgNOR is one of such marker which seems highly sensitive and specific to distinguish between benign and malignant thyroid lesions in smears because more accuracy is ensured after whole nuclei have beenassessed.6

The study was undertaken with aim of evaluating diagnostic efficacy of AgNOR staining in FNAC of thyroid lesions along with cytomorphological features. Thyroid cytology comprised 8.4% of total FNACs conducted at our institution in the study period. This is in accordance with the study by Chalise et al(2013), where 8.79% of cases were of thyroid.11

In this study ,number of benign cases was 131 which is closest to the benign cases of the study done by Hossian Et al (2012).8 The overall mean AgNOR count of benign thyroid lesions was 2.20±1.06, which is in accordance with all the studies. The study done by Mehrotra et al (1998)10 had mean AgNOR count of benign lesions (2.28), which was closest to our study. Comparison of Mean AgNOR Scores and Standard Deviation (SD) in Benign Thyroid lesions is shown in Table 3.

Number of malignant cases was 19 which is closest to the malignant cases of the study done by Hossian Et al (2012).8 The overall mean AgNOR count of malignant thyroid lesions was 4.92±1.71 which is in accordance with all the studies. The study done by Eroz et al (2011) 9 had mean AgNOR count of malignant lesions (4.6), which was closest to our study. Comparison of Mean AgNOR Scores and Standard Deviation (SD) in Malignant Thyroid lesions is shown in Table 4 .

In this study, overall mean AgNOR score of malignant thyroid lesions(4.92) was found to be considerably higher than overall mean AgNOR score (2.20) of benign thyroid lesions. This was in accordance with other studies which also showed higher mean AgNOR score of malignant thyroid lesions. In the study done by Eroz et al(2013),16 they found a cut-off value for differentiating normal thyroid tissue from benign nodules. AgNOR count was<1.5 in thyrocytes obtained from normal thyroid tissue, AgNOR count was between 1.5 and 2.9 for benign thyroid lesions. In this study, the mean AgNOR score of benign thyroid lesions (2.20) was found to be in the range of benign thyroid lesions given by Eroz et al(2013)16

Derenzini et al (2000) has stated in their study that a rapidly dividing cell must concentrate its ribosomal biogenesis in a shorter time than a slowly dividing cell. This can be achieved by activating a greater number of rDNA sequences for transcription. For this reason, a greater quantity of AgNOR proteins must be synthesised, which will increase the number of interphase AgNORs, the structural–functional units for rRNA synthesis.17

Hence, malignant cells should have higher AgNOR count. Eroz et al (2013) 16 have found that cutoff AgNOR count for cancer group which was >2.9. which supports the mean AgNORcount for malignant thyroid lesions (4.92) found in this study.

Analysis of the present study has shown statistically significant differences in AgNOR scores between benign and malignant lesions (P value = 0.00).

In the present study mean AgNOR count was highest inmetastatic deposits of squamous cell carcinoma (10.2) and lowest in Hashimoto’s thyroiditis, Hyperplastic goiter, and colloid goitre(1.8). Asotra et al (2008) 6 found highest meanAgNOR count in papillary carcinoma (5.08) andlowest in Hashimoto’s thyroiditis (2.76). Mehrotra et al(1998) 10 found highest mean AgNOR count in follicular carcinoma (5.04) and lowest in case of thyroiditis(1.37 ). Khan et al (1996). 18 found highest mean AgNOR count in follicular carcinoma (2.85) and lowest in adenomatous goitre (1.92). Comparison of Mean AgNOR Scores and Standard Deviation (SD) in different thyroid lesions is shown in Table 5.

In the present study, only 18 cases underwent surgery for which histopathological correlation was available. The mean AgNOR count of various thyroid lesions were similar to the study done by Chalise et al(2013).11

The present study had 6 cases in which diagnosis of suspicious of papillary carcinoma was made. Out of these 6 cases, histopathological correlation was available in 5 cases. Concordant diagnosis of PTC was made in 4 cases and discordant diagnosis was made in 1 case. Single case of suspicious of PTC on FNAC was Sclerosing variant of HT on histopathology. Mean AgNOR count (3.2) for this case was within the range of AgNOR count of HT.

The Mean AgNOR count of all suspicious cases was 4.81 which was in accordance with the study done by Hossain et al(2012), 8 who found that in all suspicious cases mean AgNOR count was greater than 3.

This study had included the newer entity of Bethesda system of reporting thyroid cytopathology (2017) which was NIFTP.15 The mean AgNOR count for NIFTP was 3.63±0.32. In this study mean AgNOR count of NIFTP was compared with PTC by Student t test, which was statistically significant. Mean AgNOR count of NIFTP (3.63±0.32) was less as compared to PTC (5.27±1.11).

In the present study, mean AgNOR count of FTC was higher than FA, which is in accordance with other studies. Mean AgNOR count of FTC was closest to the mean AgNOR in Study by Chalise et al(2013). 11 Mean AgNOR count of FA was closest to the mean AgNOR count by Augustynowicz et al(2004). 19 However, no significance was found (P value=0.237) when both FTC and FA were compared by student t test.

Limitations: One of the limitations of our study was lower biopsy sample for histopathological confirmation and also of unavailability of cases from every series, specially neoplastic cases.

Conclusion

Fine needle aspiration cytology is a very efficient, cost-effective and safe procedure for the diagnosis of thyroid lesions, but it is largely subjective and in a minority of cases a correct diagnosis cannot be made due to the existence of grey zone lesions. AgNOR staining can be used as an adjunct to FNAC for diagnosis of benign and malignant thyroid lesions. The grey zone lesions such as follicular adenoma and follicular carcinoma, which could not be differentiated only on the basis of FNAC, AgNOR count can be utilized as an additional tool in the cytological evaluation of follicular neoplasms.

Acknowledgement

Dr. MG Shivaramu, Principal Adichunchanagiri Institute of Medical Sciences, BG Nagara for the help and support provided.

Sources of Funding

None.

Conflict of Interest

None.

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