MINI REVIEW article
Application of liquid-based cytology to fine-needle aspiration biopsies of the thyroid gland
- 1 Division of Anatomic Pathology and Histology, “Agostino Gemelli” School of Medicine and Hospital, Università Cattolica del Sacro Cuore, Rome, Italy
- 2 Division of Anatomic Pathology and Histology, “Tor Vergata” University of Rome, Rome, Italy
- 3 Division of Endocrine Surgery, “Agostino Gemelli” School of Medicine and Hospital, Università Cattolica del Sacro Cuore, Rome, Italy
- 4 Division of Endocrinology, “Agostino Gemelli” School of Medicine and Hospital, Università Cattolica del Sacro Cuore, Rome, Italy
Fine-needle aspiration biopsy is regarded as an important tool for diagnosing thyroid lesions because of its simplicity, safety, and cost–effectiveness. Its role in correctly characterizing the group of indeterminate lesions or follicular-patterned neoplasms (FN) might be more decisive. Liquid-based cytology (LBC) is a technique based on the use of a semi-automated device that has gained popularity as a method of collecting and processing both gynecologic and non-gynecologic cytologic specimens. It achieves a diagnostic sensitivity as accurate as conventional preparations especially for its excellent cell preservation and for the lack of background which decrease the amount of inadequate diagnoses. Moreover, the cellular material which has been stored in the preservative solution could be effectively used for the application of immunocytochemical and molecular techniques especially for the Follicular proliferations. In many cases the cytologic features are similar in both methods but the colloid film and the lymphocytic component are more easily evaluated on direct smears whereas nuclear details and colloid globules are better evaluated in LBC slides. The LBC-processed biopsies represent a valid alternative to conventional cytology. The possibility of applying special techniques enhance the efficacy of the cytological diagnosis of thyroid lesions.
Fine-needle aspiration biopsy (FNAB) represents an invaluable diagnostic tool for characterizing thyroid nodules with a worldwide consensus for its simplicity, safety (Galera-Davidson and Gonzalez-Campora, 2008), and regarded as the most accurate and cost–effective method for the selection of surgical patients.
The liquid-based cytology (LBC) technique, originally developed for application to gynecologic cervical smears, has progressively gained consensus for both non-gynecologic and fine-needle aspiration cytological material (Biscotti et al., 1995; Rossi and Fadda, 2008; Rossi et al., 2009).
This method is based on a two-step procedure: (1) the fixation of the material in an methanol-based solution and (2) the automated processing of the material to obtain a thin layer of cells with a computer-assisted device. The two most common methods for processing the cytologic samples are: ThinPrep2000™ (Hologic Co., Marlborough, MA, USA), in which the cells are aspirated from a methanol-based solution (Cytolyt™) then filtered and transferred onto a positively charged slide with a gentle positive pressure; in the method SurePath™ (TriPath Imaging, Burlington, NC, USA) the cells are collected in an ethanol-based solution (CytoRich™), centrifuged twice then slowly sedimentated onto a poly-L-lysinated slide and eventually stained with a specific hematoxylin–eosin stain. The final result for both methods is one slide for each lesion with all cells concentrated in the central area of the slide with a sensitivity of 77% and a specificity of 81% (Geers and Bourgain, 2011).
Despite the initial controversy regarding the efficacy of the use of Thin Prep alone (Cochand-Priollet et al., 2003; Fadda et al., 2006; Rossi et al., 2010) good results have been achieved by many groups in different countries, especially in the recent years. Since November 2003 until 2011 the majority of about 22,000 FNABs carried out in the “Agostino Gemelli” School of Medicine and Hospital of Rome have been processed by ThinPrep2000™ alone. This experience has been reported in many studies published since 2005 where the efficacy of the ThinPrep2000™ technique for a correct pre-operative diagnosis of more than 500 malignant neoplasms is highlighted. In the study by Rossi et al. (2009), three parameters of efficacy (inadequacy, indeterminacy, and malignancy rates) were chosen for evaluating the efficacy of ThinPrep2000™ in comparison with CS alone and combining ThinPrep2000™ and CS in more than 10,000 thyroid FNAB showing that ThinPrep2000™ alone was as effective as CS in decreasing both inadequate and indeterminate diagnoses (Fadda et al., 2011b). The study of Geers and Bourgain (2011) using the SurePath method achieves controversial results in terms of inadequacy rate between LBC and SurePath.
The ThinPrep2000™ material stored in the vial can be used for additional techniques such as immunocytochemistry, flow cytometry, and molecular biology (Cochand-Priollet et al., 2003; Rossi et al., 2005).
Cytology of LBC-Processed Thyroid Lesions
The morphologic picture of LBC differs mainly from CS in two aspects: (a) the cells in each slide are a monolayered representative sample of the entire material collected in the vial with a variable amount of cells which remains in the preservative solution; (b) the automated process causes some changes in both cellular and background morphology. One of the most important change, occurring in LBC slides, is the appearance of the fragmented colloid which is present as small droplets in the background of a benign nodule with a quantitative detection whereas in CS the colloid usually does not require a quantization (Figure 1; Biscotti et al., 1995). The LBC picture of a thyroiditis is similar to CS with the exception of the amount of lymphocytes in the background which can be higher than normal because of the spinning of the material before the automated process. When a thyroiditis is suspected, the detection of lympho-epithelial clusters in an inflammatory background is the pivotal clue for the diagnosis and warrants a simple follow-up for the patient (Das, 2006).
Figure 1. A case of colloid goiter exhibiting small clusters of monomorphic follicular cells mixed with colloid droplets (LBC, Papanicolaou, 400×).
There are very few differences in the cytologic pictures of follicular neoplasms (FN) in LBC versus CS based upon the identification of microfollicles made up of medium-sized thyrocytes in scant colloid. The amount and morphology of the follicular cells allow the inclusion of an individual lesion in one of the categories that have been recently devised in Europe and in the USA with three possible scenario (British Thyroid Association, 2007; Baloch et al., 2008; Fadda et al., 2010):
(1) The first scenario is represented by a lesion which high cellularity but the cells are monomorphous with occasional enlarged nuclei. This lesion may correspond to the cellular adenomatous nodule and is usually included in the non-neoplastic category of the European classifications (Thy 2 by BTA classification, TIR 2 by Italian classification,). On the other hand, the Bethesda classification has established a different category for this picture which is defined as “follicular lesion with undetermined significance (FLUS)” or “atypical cells of undetermined significance (ACUS or AUS)” with a different risk of malignant occurrence which in the American classification is stated between 5 and 15% (mostly follicular carcinoma) whereas in the European systems is closer to non-neoplastic lesions (British Thyroid Association, 2007; Baloch et al., 2008; Fadda et al., 2010).
(2) The second scenario is represented by a lesion mostly follicular-structured and made up of medium-sized thyrocytes with rounded nuclei and central nucleolus (Follicular Neoplasm) with a malignancy risk between 20 and 30%. The action, although debated in the literature, results in the surgical removal of the lesion which could histologically correspond to both a follicular adenoma or an adenomatous nodule in a goiter (70–80% of cases) but also follicular carcinoma or a follicular variant of a papillary carcinoma (PC) cannot be ruled out only on morphology. The same diagnostic criteria and therapeutic action is applied to the FN composed mostly by oxyphilic (or Hurthle) cells which is defined when follicles are made up of more than 80% of oxyphilic cells and it should be included in the FN category (Thy 3 of the BTA, TIR 3 of the Italian classifications). The colloid amount may be scant (but sometimes is abundant) and features of old hemorrhage (hemosiderin-laden histiocytes) may coexist (Giorgadze et al., 2004; British Thyroid Association, 2007; Baloch et al., 2008).
(3) The third scenario is represented by follicular-structured lesions, composed by thyrocytes with elongated and clear nuclei, sometimes with grooves and peripheral nucleoli without papillae, psammomatous bodies, or nuclear pseudoinclusions with a risk of malignancy ranging between 50 and 70%. This category warrants the surgical removal of the nodule as a follicular variant of a PC is very likely to be found at the histological examination (more than 90% of cases).
The cytological diagnosis of thyroid malignancy does not differ substantially in LBC preparations as the clear background facilitates the identification and characterization of the cellular details.
The most important malignant tumor which can be appropriately identified on LBC preparations is PC which is easily when nuclear pseudoinclusions are detected (Figure 2) papillary structures and psammoma bodies are seldom identified. In the earlier reports, the difficulty in detecting the distinctive nuclear features of PC was one of the most important objections against the adoption of the thyroid LBC cytology.
Figure 2. A distinctive nuclear pseudoinclusion in a fine-needle aspiration biopsy from a thyroid papillary carcinoma (LBC, Papanicolau, 400×).
Medullary thyroid carcinoma (MTC) is a difficult cytological diagnosis. The LBC technique offers the opportunity to detect the calcitonin expression in the neoplastic parafollicular cells and their concomitant negativity for thyroglobulin (Rossi et al., 2008).
Anaplastic thyroid carcinoma (ATC) is seldom seen in routine thyroid cytology. The LBC picture of ATC usually shows a background of necrotic debris with small clusters of large round or spindle cells with pleomorphic nuclei and prominent nucleoli which stains positive for cytokeratins (useful to confirm the epithelial origin) and negative for thyroglobulin and TTF-1. The LBC diagnosis of the large cell variant of malignant non-Hodgkin lymphoma usually does not constitute a problem and relies on the immunocytochemical expression of LCA, CD20, bcl-6, and other lymphoid antigens.
Lung, breast, kidney, large bowel, and laryngeal metastatic carcinomas to the thyroid gland may occasionally present as a single nodule mimicking a primary tumor in which necrotic debris or hemorrhagic material and clusters of neoplastic cells with features of adenocarcinoma or squamous cell carcinoma are detected on Cs and ThinPrep2000™
Immunocytochemistry was introduced in the early 1970s for the definition of the nature of the lesions, especially in the differential diagnosis between follicular and C-cell derived neoplasms and in the identification of primary or metastatic thyroid neoplasms (e.g., malignant lymphoma) even if the main role is the identification of the markers of malignancy which may distinguish malignant from benign lesions regardless of the presence of capsular and vascular invasion (Rossi et al., 2006).
There have been only few reported experiences in literature dealing with ICC applied on ThinPrep2000™. The use of ICC on the cells stored in the preservative ThinPrep2000™ solution yields excellent results with most immunoreagents in terms of staining pattern, intensity of the reaction and less amount of reagent due to the clear background and smaller size of the ThinPrep2000™ slide (Dabbs et al., 1997; Leung and Bedard, 1999; Rossi et al., 2006).
In our practice and based on the data in the literature, no “magic single marker” may be useful but only the concordance of a panel should be considered especially in cases of follicular lesions. The use of more than one immunomarker is a further guarantee for a correct diagnostic approach, especially when a concordant panel is expressed (Rossi et al., 2006) and with excellent results also in the differential diagnosis between benign and malignant follicular neoplasms (Dabbs et al., 1997; Leung and Bedard, 1999; Schmitt et al., 2008; Fadda et al., 2011a).
HBME-1, Galectin-3, and RET proto-oncogene have shown the best specificity and sensitivity in discriminating benign from malignant differentiated tumors. These data emerged from one of the paper of our group, in which the combination of nuclear pleomorphism and positivity of the panel resulted in 75% specificity and 89% diagnostic accuracy of FNAB (Rossi et al., 2005). In another study recently published by our group, the complete immunocytochemical panel (made up of HBME-1 and Galectin-3) was positive in 83.3% of malignancy and negative in 87.5% benign histological cases. In the group of FN/AUS (according to the Bethesda system), the expression of HBME-1 and Galectin-3 on LBC can effectively distinguish lesions which need immediate surgery (high risk FN) from those which can be followed-up (low risk FN).
Recent advances in molecular genetics of thyroid cancer are being applied for developing new diagnostic markers for FNA samples in an attempt to differentiate benign from malignant thyroid nodules (Nikiforova and Nikiforov, 2009). PC, the most common thyroid malignancy, may carry BRAF, Ret/PTC, or RAS mutations (Nikiforova and Nikiforov, 2009). These mutually exclusive somatic mutations are found in more than 70% of PCs with a more aggressive tumor behavior such as extra-thyroidal extension, advanced tumor stage at presentation and lymph node or distant metastases (Xing, 2007).
Several studies have demonstrated the feasibility of detecting BRAF, RET/PTC, or RAS mutation in thyroid FNA samples and have shown that this may improve the cytological FNA diagnosis (Nikiforova and Nikiforov, 2009; Ohori et al., 2010; Fadda et al., 2011b).
A recent paper by Nikiforova and Nikiforov (2009) explored the diagnostic utility of molecular testing for a panel of molecular mutations consisting on BRAF, RAS, RET/PTC, and PAX8–PPARγ in 480 FNA samples from thyroid nodules which were prospectively tested and yielded 32 mutations with 31 malignant surgical diagnoses and only one case of follicular adenoma.
The possible diagnostic use of molecular markers is reflected in the last guidelines published by the American Thyroid Association. These guidelines indicate that the use of molecular markers such as BRAF, RAS, RET/PTC, and PAX8–PPARγ may be considered (with low recommendation rate) for patients with indeterminate FNA cytology to help guide their clinical management.
As resulted in our preliminary study the evaluation of BRAF positivity could be a prognostic value for the presence of nodal metastases and the presence of BRAF positivity performances to the surgical neck central dissection and also to the detection of any other nodal possible implication (Fadda et al., 2011b).
Liquid-based cytology can offer the possibility of immunocytochemical evaluation and molecular testings for common somatic mutations in thyroid FNAB as the nucleic acids are stable in the preservative solution up to 6 months after the sampling. In this setting, the future possibility of a guideline encompassing the combined use of immunocytochemistry and molecular tests for supplementing the morphologic diagnosis could be the starting point for a complete pre-operative assessment of a thyroid lesion.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: thyroid nodules, fine-needle aspiration cytology, liquid-based cytology
Citation: Rossi ED, Zannoni GF, Moncelsi S, Stigliano E, Santeusanio G, Lombardi CP, Pontecorvi A and Fadda G (2012) Application of liquid-based cytology to fine-needle aspiration biopsies of the thyroid gland. Front. Endocrin. 3:57. doi: 10.3389/fendo.2012.00057
Received: 12 January 2012; Accepted: 03 April 2012;
Published online: 16 May 2012.
Edited by:Carmelo Nucera, Beth Israel Deaconess Medical Center/Harvard Medical School, USA
Reviewed by:Marialuisa Appetecchia, Regina Elena National Cancer Institute IRCCS, Italy
William C. Faquin, Massachusetts General Hospital, USA
Copyright: © 2012 Rossi, Zannoni, Moncelsi, Stigliano, Santeusanio, Lombardi, Pontecorvi and Fadda. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: Guido Fadda, Division of Anatomic Pathology and Histology, “Agostino Gemelli” School of Medicine and Hospital, Università Cattolica del Sacro Cuore, Largo Francesco Vito, 1 00168 Rome, Italy. e-mail: firstname.lastname@example.org