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Annals of Surgical Treatment and Research logoLink to Annals of Surgical Treatment and Research
. 2018 Apr 30;94(5):229–234. doi: 10.4174/astr.2018.94.5.229

Extent of central lymph node dissection for papillary thyroid carcinoma in the isthmus

Young Woo Chang 1, Hye Yoon Lee 1, Hwan Soo Kim 1, Hoon Yub Kim 1, Jae Bok Lee 1, Gil Soo Son 1,
PMCID: PMC5931932  PMID: 29732353

Abstract

Purpose

The incidence of papillary thyroid carcinoma (PTC) arising from the isthmus is low; however, these tumors have aggressive clinical and pathological features. Moreover, the existing guidelines regarding the extent of surgery for this type of tumor are unclear.

Methods

This study enrolled 282 patients who underwent total thyroidectomy with bilateral central lymph node dissection. The patients were divided into 2 groups based on the location of the median line of the PTC. Group I included patients in whom the median line was located between the lateral margins of the trachea; group II included all others. We compared the 2 groups and conducted a multivariate analysis to assess risk factors for contralateral node metastasis from a PTC arising from the isthmus.

Results

Patients in group I had significantly higher frequencies of extrathyroidal extension and central lymph node metastasis. Group I also had a higher frequency of contralateral node metastasis, and a tumor size >1.0 cm was identified as an independent risk factor for contralateral node metastasis among patients in this group.

Conclusion

Bilateral central lymph node dissection could be considered for patients with isthmic PTCs >1.0 cm in size who have clinically suspicious node metastasis.

Keywords: Papillary thyroid carcinoma, Papillary thyroid microcarcinoma, Lymph node excision

INTRODUCTION

The thyroid isthmus is a small tissue segment that connects both thyroid lobes and is adjacent to the trachea anteriorly and strap muscles dorsally. Papillary thyroid carcinomas (PTCs) rarely arise from the isthmus; however, these tumors exhibit relatively more aggressive features, such as multifocality, extrathyroidal extension, and lymphovascular invasion, compared to those arising from the thyroid lobes [1,2,3].

Central lymph node metastasis is frequently observed in patients with PTC, with reported incidences ranging from approximately 20% to 39% [4,5,6,7,8]. Furthermore, PTC in the isthmus, or isthmic PTC, tends to more strongly associate with central lymph node metastasis, compared to lobar tumors [9]. However, the 2015 American Thyroid Association guidelines and 2017 National Comprehensive Cancer Network guidelines lack recommendations regarding central lymph node dissection for patients with isthmic PTC [10,11].

To our best knowledge, although some studies have addressed the extent of thyroidectomy for patients with PTC arising in the isthmus, few have discussed the extent of central lymph node dissection. Therefore, in this study we compared clinicopathological findings by PTC location and investigated the risk factors for contralateral node metastasis in patients with isthmic PTC.

METHODS

Study population

Between January 2008 and December 2016, we retrieved the records of 1,421 patients with PTC who underwent thyroidectomy with central neck lymph node. Among these, 575 patients who underwent hemi-thyroidectomy and 62 patients who underwent lateral neck lymph node dissection were excluded. To avoid the influence of lymph node metastases from multifocal thyroid tumors and focus the analysis only on contralateral lymph node metastasis, 347 patients with multiple tumors and 155 patients who underwent only ipsilateral central lymph node dissection were also excluded. Finally, 282 patients who underwent total thyroidectomy with bilateral central lymph node dissection remained eligible and were divided into 2 groups as described below (Fig. 1). At out institute, bilateral central lymph node dissection was performed in patients with clinically suspicious node metastasis in preoperative radiologic findings or intraoperative suspicious node metastasis. This retrospective study was approved by the Institutional Review Board of Korea University Medical Center, Ansan (approval number: AS17032). A waiver of informed consent was requested, and approval was obtained.

Fig. 1. Flowchart of patients with papillary thyroid cancer in this study. Group I, patients had isthmic tumors; group II, patients had lobar tumors.

Fig. 1

Definitions

The preoperative ultrasonography findings of all 282 patients in this study were reviewed; the patients were divided into 2 groups based on the location of the median line of the PTC. Group I included patients in whom the median line of the PTC was located between the lateral margins of the trachea; group II was defined as all other eligible patients with PTC. Each group was further subdivided as follows for the contralateral central lymph node analysis: right lobe, left lobe, right isthmus, and left isthmus (Fig. 2).

Fig. 2. (A) Ultrasonogram of a papillary thyroid carcinoma (arrow) in the isthmus. (B) Schematic illustration of the structures used to define groups in this study. Tumors (solid circle) for which the median line (arrow) was located between the lateral margins of trachea were classified as group I; all others (dotted circle) were classified as group II. RL, right lobe; RI, right isthmus; LI, left isthmus; LL, left lobe.

Fig. 2

Surgery and pathologic examination

Central lymph node dissection was performed with the following boundaries: the hyoid bone superiorly, the carotid sheath laterally, the manubrium inferiorly, and the prevertebral fascia dorsally. The central lymph nodes were divided into right and left using the median line of the trachea, and the Delphian nodes were included as ipsilateral lymph nodes. The entire surgical thyroid specimen and central lymph nodes were sent for pathologic examination, and the histologic findings were recorded and analyzed. TNM staging was performed according to the American Joint Committee on Cancer staging manual (8th edition).

Statistical analysis

Continuous data are presented as medians with ranges, and Student t-test was used to compare 2 groups. For both groups, the number of metastatic lymph nodes is presented as a mean value with a range because many patients had no lymph node metastases. Categorical data are presented as numbers with percentages and were compared using the chi-square test or Fisher exact test. A binary logistic regression was used to conduct the multivariate analysis. Differences were considered statistically significant at a P-value of <0.05. All data were analyzed using IBM SPSS Statistics ver. 24.0 (IBM Co., Armonk, NY, USA).

RESULTS

Patient and tumor characteristics

The patient and tumor characteristics are listed and compared in Table 1. The study population included 71 patients assigned to group I and 211 assigned to group II. The mean age at the time of surgery (43.2 ± 12.0 vs. 45.6 ± 11.5, respectively, P = 0.13) and the proportion of patients older than 55 years did not differ significantly between the groups. Similarly, no significant differences were observed in the sex ratio, mean tumor size (1.2 ± 0.7 vs. 1.4 ± 0.6, respectively, P = 0.10), and the proportion of patients with tumors >1.0 cm in size. Patients in group I had a significantly higher frequency of extrathyroidal extension, compared to those in group II (47.9% vs. 29.4%, respectively, P < 0.01). The 2 groups had similar frequencies of lymphovascular invasion and thyroiditis. TNM staging did not differ between the 2 groups (Table 1).

Table 1. Clinicopathological characteristics of all patients with PTC in this study (n = 282).

graphic file with name astr-94-229-i001.jpg

Values are presented as median (range) or number (%).

Group I, patients had isthmic tumors; group II, patients had lobar tumors; PTC, papillary thyroid carcinoma.

Detailed comparison of the aspects of central lymph node metastasis

The mean number of harvested lymph nodes was comparable between the 2 groups (10.42 ± 2.98 vs. 9.60 ± 3.26, respectively, P = 0.06); however, the mean number of metastatic lymph nodes was significantly higher in group I (2.17 ± 2.16 vs. 0.87 ± 1.33, respectively, P < 0.01). Patients in group I also had a higher frequency of central lymph node metastasis, compared with group II (69.0% vs. 42.2%, respectively, P < 0.01). Regarding the location of lymph node metastasis, no significant differences were observed with respect to ipsilateral node metastasis. However, the frequency of bilateral node metastasis was significantly higher among patients in group I, compared to group II (21.1% vs. 3.8%, respectively, P < 0.01). No patients in this study had only contralateral node metastasis (Table 2).

Table 2. Incidence of central lymph node metastasis in patients with PTC in this study (n = 282).

graphic file with name astr-94-229-i002.jpg

Group I, patients had isthmic tumors; group II, patients had lobar tumors; PTC, papillary thyroid carcinoma; LN, lymph node; RI, right isthmus; LI, left isthmus; RL, right lobe; LL, left lobe.

Risk factors for contralateral node metastasis

Table 3 lists the evaluated risk factors for contralateral node metastasis in patients with isthmic PTC. The univariate analysis revealed that a tumor size > 1.0 cm was significantly associated with contralateral node metastasis (P < 0.01). No other risk factors were found to associate with contralateral node metastasis. After all variables were included in the binary logistic regression model for the multivariate analysis, a tumor size > 1.0 cm remained an independent risk factor for contralateral node metastasis.

Table 3. Risk factors for contralateral central lymph node metastasis in patients with PTC arising from the isthmus (n = 71).

graphic file with name astr-94-229-i003.jpg

PTC, papillary thyroid carcinoma; OR, odds ratio; CI, confidence interval.

DISCUSSION

The reported incidence of PTC arising from the isthmus has ranged from 2.5% to 12.3% in recent studies [2,12,13,14]. At our institute, the incidence of PTC arising from the isthmus was 10.2% (145 of 1421 patients) during the study period, regardless of the type of surgery, and was comparable with that of previous studies.

Despite its low incidence, isthmic PTC is associated with more aggressive clinical and pathological features. In our study, the frequencies of extrathyroidal extension and central lymph node metastasis were higher in group I, even though the groups did not differ with respect to other clinicopathological characteristics. Previous studies also reported that patients with PTCs located in the isthmus had poorer prognoses, compared to patients with lobar PTCs [2,3,13,14]. The aggressive clinicopathological features of isthmic PTC might be attributable to the thin shape of the isthmus, which could facilitate the invasion of adjacent tissues.

In this study, the incidences of central lymph node metastasis in groups 1 and 2 were 69.0% and 42.2%, respectively, slightly higher than in other studies of central lymph node metastasis from PTC [4,5,6,7,8]. We could attribute this difference to the determination of total thyroidectomy with bilateral central lymph node dissection, which was based on the surgeon's decision in cases with clinically suspected node metastasis on preoperative imaging studies [15,16]. However, our findings were agreed with similar reports stating that patients with isthmic PTC tend to have higher frequencies of central lymph node metastasis.

The definitions of the isthmus used in previous studies were discordant or unclear. We defined a PTC of the isthmus as a tumor in which the median line was located between the lateral margins of the trachea [17]. Because if most of the tumor is located in the trachea despite the tumor margin beyond the boundaries of the trachea, the tumor would have characteristics of a PTC arising from the isthmus rather than from the lobes. Therefore, we reviewed the preoperative ultrasonographic findings of all patients who underwent total thyroidectomy with bilateral central lymph node dissection in this study to facilitate subgroup classification.

Lymphatic drainage travels more frequently from the isthmus, compared to the lobes, to the prelaryngeal and pretracheal nodes and then spreads to the paratracheal node [18,19,20]. Therefore, we hypothesized that an isthmic PTC would confer a stronger risk of contralateral node metastasis than a lobar PTC, and accordingly analyzed the correlation between contralateral node metastasis and tumor location. The rate of contralateral node metastasis was indeed significantly higher in group I. Although no patients had only contralateral node metastasis, the frequencies of bilateral node metastasis in groups 1 and 2 were 21.1% and 3.8%, respectively. A previous study with a similar concept also reported an increased frequency of contralateral node metastasis among patients with isthmic PTC and suggested bilateral central lymph node dissection for this population [21]. Although we agreed with that suggestion, only 21.1% (15 of 71) of patients in our group 1 presented with contralateral node metastasis; therefore, an analysis of risk factors for contralateral node metastasis of isthmic PTC was needed.

A binary logistic regression modal was used to conduct a multivariate analysis of risk factors for contralateral node metastasis in group I; here, we identified a tumor size > 1.0 cm as an independent risk factor for contralateral node metastasis. Isthmic PTC is believed to more frequently exhibit extrathyroidal extension, which is associated with total central lymph node metastasis; however, in contrast to our expectations, extrathyroidal extension was not found to be an independent risk factor in this study. Most patients with contralateral node metastasis had a tumor size > 1.0 cm, whereas only 2 cases (2 of 36, 5.6%) involving tumors ≤ 1 cm in size had contralateral node metastases, although the tumors were isthmic. In summary, larger isthmic PTCs might have more opportunities to spread through contralateral lymphatic channels. Hence, our results suggest that bilateral central lymph node dissection could be considered for patients with isthmic PTCs > 1.0 cm in size who have clinically suspicious node metastasis.

The limitations of this study include its retrospective design, which introduces the risk of bias. In this study, the number of patients with PTCs arising from the isthmus and central lymph node metastases was relatively small. Moreover, the central lymph nodes were classified only into right and left subgroups, but not into subsite groups, given our lack of data. Therefore, we could not conduct analyses based on central lymph node subsites and predict spreading patterns of lymph node metastases from isthmic PTCs. Our study did not present the greatest dimension of metastatic lymph nodes. We have started measuring the size of metastatic lymph node in recent years and data based on its size could not be analyzed. Accordingly, our results must be interpreted cautiously, and a randomized controlled study is needed to overcome these limitations.

In conclusion, central lymph node metastasis occurred more frequently in patients with isthmic PTC than in those with lobar PTC. In the former group, contralateral node metastasis was more commonly observed in patients with tumors > 1.0 cm in size. Therefore, bilateral central lymph node dissection could be considered for patients with isthmic PTCs that exceed this size threshold when node metastasis is suspicious clinically.

Footnotes

CONFLICTS OF INTEREST: No potential conflict of interest relevant to this article was reported.

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