In the investigation of thyroid nodules, there is a need to safely select nodules for FNA cytological analysis to maximise benefits and minimise cost, given the high incidence of thyroid nodules [6, 10]. Evidence is gathering that the malignant potential of thyroid nodules may not be strongly associated with nodule size or palpability or whether they are solitary or occur in a multinodular gland [1, 2, 5–8, 10]. Clinical risk factors such as a history of head and neck irradiation, thyroid cancer, a family history of thyroid cancer or familial adenomatous polyposis, rapid growth, vocal cord paralysis and regional lymphadenopathy [1, 6, 8] are uncommon. There is thus increasing reliance on ultrasound and colour Doppler, by virtue of certain specific characteristics for detecting malignancy, to select nodules for FNA or biopsy [2]. It has also been recommended that in a multinodular gland FNA should be targeted by suspicious ultrasound features rather than by a nodule being clinically dominant [2, 5, 6].
In our service evaluation study, we have tested a set of ultrasound and colour Doppler selection criteria for detecting malignant nodules and selecting them for FNA cytology (Table 5). The characteristics of calcification, mixed colour flow pattern and markedly hypoechoic echo texture (Fig. 2) all have high odds ratios on the logistic regression (multivariable) analysis. In particular, microcalcification is the most specific sign, with all the five nodules demonstrating it being malignant. A sensitivity of 100 % (Table 6) is obtained making it a safe approach with all malignant nodules ‘earmarked’ and selected for FNA cytology. Even though this selection criterion has a lower specificity of 76 %, we have demonstrated that it can reduce substantially the number of required FNA biopsies. In our series of 171 patients, 117 out of the 153 benign nodules (Fig. 3) would not have required FNA cytology analysis to establish benignity if the selection criterion (Table 5) was applied in the first instance, with consequent benefit to both patient and service provision and reduction in cost.
The lower specificity is due to 36 false-positive cases. The most common nodular characteristic leading to false positive diagnosis is the presence of central or mixed colour flow pattern on Doppler ultrasound seen in 32 out of 36 false-positive cases (Fig. 4). But it is this characteristic that is the only abnormal characteristic in 6 of the 18 malignant nodules. The high sensitivity and lower positive predictive value of colour Doppler pattern in detecting malignancy is well documented in other studies [7, 12, 13]. A less common cause of false-positive result is marked hypoechogenicity (five cases). It is, however, the only abnormal feature in two malignant nodules. Seven out of eight cases of coarse calcification were false-positive for malignancy and in the one case of malignancy with coarse calcification, florid intranodular colour flow was also seen. By contrast, all five cases of microcalcification were malignant nodules, making it the most specific sign for malignancy. This sign is, however, also associated with either marked hypoechogenicity or marked intranodular colour flow in four out of five cases. Of a particular note is one case of histologically proven follicular carcinoma which had two non–diagnostic Thy1 cytology results preoperatively. This nodule was markedly hypoechoic and had marked central vascularity on ultrasound. Hence, in the case of a nodule where cytology is repeatedly non-diagnostic, ultrasound with colour Doppler can be valuable in helping the surgeon decide on surgery.
With regards to prospective studies investigating the use of ultrasound with colour Doppler [7, 9, 14, 15], our study is, to our knowledge, the larger of two prospective studies [14] testing the diagnostic performance of a set of ultrasound and colour Doppler criteria in detecting malignancy in palpable and non-palpable thyroid nodules, where the final diagnosis is established by histology for all malignant and indeterminate nodules and cytology with follow-up for all nodules with benign cytology. In a smaller study of 66 patients (78 thyroid nodules), Yunus et al. [14] demonstrated a slightly lower sensitivity and specificity of 93.8 % and 66 % respectively compared with ours in detecting malignancy for a set of selection criteria that are similar to ours but also included a taller than wide shape of the nodule and nodular irregularity/microlobulations. Their study, however, included only solid nodules (cystic nodules excluded).
In interpreting the results, it is important to note the limitations of our prospective study. Our study is part of a service evaluation with the aim of informing the evidence around rationalising selection for FNA. Many patients in our hospital catchment area are managed in primary care by general practitioners who refer mainly more complex cases to our clinic. In addition, there is selection bias with many nodules, with benign cytology being excluded from the study, having not being followed-up as part of the criteria to establish benignity. Bias is also introduced as nodules are not randomly selected for FNA in a multinodular gland but selected by size or atypical ultrasound features. Having said this, 10 % of the cases in our sample were malignant and comparable with an overall incidence of 9.2–13 % in patients with thyroid nodules selected for FNA [1]. Even though our sample size is smaller than the few other prospective studies [7, 9, 15] evaluating thyroid ultrasound characteristics with colour Doppler, it is the largest prospective study to date investigating the use of a set of ultrasound and colour Doppler criteria in selecting malignancy nodules for FNA or biopsy. As with many studies in the literature evaluating thyroid ultrasound characteristics, the diagnosis of a benign nodule in the majority of our patients is a cytological rather than a histological one, as these patients do not routinely undergo surgery for benign non-neoplastic nodules. We hope to offset the limitations of cytological diagnosis by performing FNA under ultrasound guidance by an experienced radiologist rather than blindly [16, 17] and with slides read by dedicated head and neck cytologists. By additionally following-up these nodules for 6 months or more to ensure stability in size [4], we hope to support the benign nature of these nodules. None of the Thy 2 nodules in our study were later classified as neoplastic on follow-up. However, we note from the observation of Ito et al. [18] that papillary microcarcinomas may not increase in size over 1- or 2-year follow-up. It may be worthwhile to note that if the study was performed in a dedicated head and neck ultrasound clinic (ultrasound being an operator-dependent procedure), the results may not be replicated by observers in a general clinic. Finally, our study uses the same dataset to determine the set of ultrasound selection criteria for detecting malignancy nodules as well as its accuracy. This requires validation by an independent dataset, preferably in the form of a larger multi-centre study.