Skip to main content
The Scientific World Journal logoLink to The Scientific World Journal
. 2013 Jan 8;2013:425136. doi: 10.1155/2013/425136

Recent Advances in the Surgical Treatment of Differentiated Thyroid Cancer: A Comprehensive Review

Raghunandan Venkat 1, Marlon A Guerrero 1,2,*
PMCID: PMC3556888  PMID: 23365543

Abstract

Differentiated thyroid cancers have become one of the fastest growing malignancies in the world. While surgery has remained the cornerstone of management of these tumors, the surgical approach has seen numerous innovations over the past few decades. The use of video-assistance and robotics has revolutionized thyroid surgery. This paper provides a comprehensive evaluation of the different approaches to thyroid surgery, the utility of prophylactic and therapeutic lymph node dissection, and evidence-based guidelines in the treatment of differentiated thyroid cancers. Minimally invasive video-ssisted thyroidectomy is both safe and effective in the hands of the trained surgeon and, in selected patient populations, has comparative perioperative morbidity and better cosmesis as compared to conventional open thyroidectomy. It is universally accepted that therapeutic central lymph node dissection should be performed when metastatic lymph nodes are identified on physical exam, ultrasound, or intraoperatively. In the absence of overt nodal metastasis, the role of elective prophylactic central lymph node dissection remains a matter of debate and prospective, randomized studies are warranted to evaluate the utility of this procedure.

1. Introduction

In the past 20 years, differentiated thyroid cancer (DTC) has become the fastest growing malignancy in the world [1]. The rise in the incidence of thyroid cancer (3.01%) is the highest in the United States with over 48,000 cases annually [2]. DTCs arise from follicular cells and include papillary (PTC), follicular (FTC), and Hürthle cell carcinoma (HCC). Surgical resection has remained the gold standard for the treatment for DTC.

Over the last two decades, there have been numerous changes in the surgical approach to thyroidectomy. Many of these include instrument innovations, such as the LigaSure, harmonic scalpel, and intraoperative nerve monitoring; while other major advances include minimally invasive surgical procedures with video assistance and robotic surgery. These changes have led to a paradigm shift in the surgical treatment of DTC.

The aim of this paper is to provide a comprehensive evaluation of the various approaches to the surgical treatment of DTC (conventional open, minimally invasive video-assisted, and endoscopic and robotic thyroidectomies) in terms of operative technique, clinical outcomes, and oncologic feasibility. We further evaluate the risks and benefits of prophylactic central lymph node dissection (CND).

2. Methods

A review of the literature was performed using Medline and Pubmed databases to identify all studies published up to October 2012 involving thyroidectomy for thyroid cancer. The MeSH search terms used were “thyroid neoplasms,” “thyroidectomy,” “endoscopy,” and “video-assisted surgery.” The above terms and their combinations were also searched as text words, as were the terms “differentiated thyroid cancer,” their subtypes (papillary, follicular, and Hürthle cell) and “robot assisted.” We excluded studies involving cancers of parafollicular origin or advanced differentiated thyroid cancer.

3. Results

Our search strategy yielded 443 studies related to the surgical treatment of DTC and we included 45 studies that discussed different approaches to the surgical treatment of DTC (conventional open, minimally invasive video-assisted, endoscopic, and robotic thyroidectomies) in terms of operative technique, clinical outcomes and oncologic feasibility as well as the utility of prophylactic and therapeutic lymph node dissection.

3.1. Risk Stratification

Various studies have evaluated risk factors and developed risk stratification systems for thyroid cancer [35]. The prognostic factors include age at diagnosis, tumor size, grade of tumor, gender, extrathyroidal extension, lymph node involvement, completeness of resection, positive margins, multicentricity, and presence of distant metastasis. Tuttle et al. [5] classified risk of death from thyroid cancer into four categories (Table 1): very low risk, low risk, intermediate risk, and high risk. Low risk features include young age at diagnosis, classical histology of PTC confined to the thyroid gland with no evidence of vascular invasion, smaller tumors (≤4 cm), complete resection, no evidence of distant metastasis, or cervical lymph node involvement. High risk features include age at diagnosis >45 years, larger tumors (>4 cm) or worrisome histology (PTC subtypes such as tall cell, columnar or insular variants, and poorly differentiated thyroid cancers), incomplete resection, vascular invasion, cervical lymph node involvement, and distant metastasis.

Table 1.

Risk of death from thyroid cancer [5].

Very low risk Low risk Intermediate risk High risk
Age at diagnosis <45 years <45 years Young patients (<45 years)
Classic PTC >4 cm
Vascular invasion
Extrathyroidal extension
Worrisome histology of
any size
>45 years

Primary tumor size <1 cm 1–4 cm Older patients (>45 years)
Classic PTC <4 cm
Extrathyroidal extension
Worrisome histology
<1-2 cm confined to the
thyroid
>4 cm classic PTC

Histology Classic PTC, confined to the thyroid gland* Classic PTC, confined to
the thyroid gland*
Histology in conjunction with age as above Worrisome histology
>1-2 cm

Completeness of resection Complete resection Complete resection Complete resection Incomplete tumor resection

Lymph node involvement None apparent Present or absent Present or absent Present or absent

Distant metastasis None apparent None apparent None apparent Present

Only those patients meeting all criteria within the respective column would be classified as very low risk or low risk. Older patients with either incomplete tumor resection or presence of distant metastasis are considered high risk irrespective of tumor size and specific histology. Patients with a combination of risk factors (age, histology, and tumor size) crossing over between columns are classified as intermediate-risk patients. PTC: papillary thyroid cancer.

*Confined to the thyroid gland with no evidence of vascular invasion or extrathyroidal extension.

Cervical lymph node metastases in older patients, but probably not in younger patients, may confer an increased risk of death from disease.

Worrisome histologies include histologic subtypes of papillary thyroid cancer such as tall cell variant, columnar variant, insular variant, and poorly differentiated thyroid cancers.

Histologically some variants of PTC have been reported to behave more aggressively. For instance the tall cell variant of PTC, which was first described by Hawk and Hazard [20] and comprises 5–10% of all cases, is more likely to be associated with high risk features such as larger size, extrathyroidal extension and distant metastasis [21]. They also have a higher incidence of progression to anaplastic carcinoma and have a higher recurrence rate and mortality, thus warranting aggressive treatment approaches [21, 22].

3.2. Surgical Approaches

Surgery remains the mainstay treatment for DTC. Total/near-total thyroidectomy and thyroid lobectomy, with or without isthmusectomy, are the two most accepted options. Total thyroidectomy is the removal of the entire thyroid gland, while preserving the parathyroid glands and the recurrent and superior laryngeal nerves. In near total thyroidectomy, which is considered equal to total thyroidectomy, a small amount of posterior thyroid capsule remains. In thyroid lobectomy, the contralateral gland is not removed. Total/near-total thyroidectomy is considered the procedure of choice for most DTCs [23]. Although some studies have shown comparable long-term results between thyroid lobectomy and total thyroidectomy in low-risk and select intermediate-risk patients [24], Bilimoria et al. [6] using National Cancer Database reported that lobectomy alone resulted in a higher risk of recurrence (hazard ratio: 1.15, P = 0.04) and death (hazard ratio: 1.31, P = 0.009) in tumors >1 cm compared to total/near-total thyroidectomy. Several studies have supported this recommendation (Tables 2 and 3) [69]. Moreover, studies have shown a 35–60% rate of occult cancer and a 6–10% rate of recurrence in the contralateral lobe. Furthermore, the removal of the entire thyroid gland facilitates the use of radioactive iodine for adjuvant therapy, measurement of serum thyroglobulin for disease surveillance, and neck ultrasonography to identify residual and/or recurrent disease. For small tumors, <1 cm confined to one thyroid lobe, with no contralateral nodules, thyroid lobectomy is an acceptable alternative. Thyroid lobectomy is a more limited procedure that avoids placing the contralateral recurrent laryngeal nerve and the parathyroid glands at risk for injury [23]. Some studies have shown greater recurrence rates with thyroid lobectomy [6], however, long-term survival does not seem to be affected [24].

Table 2.

Comparison of outcomes of lobectomy and total thyroidectomy.

Study Recurrence (%) Survival (%)
10-year+ 10-year+
Bilimoria et al. [6]
N = 52,173
TL: 9.8 TL: 97.1
TT: 7.7 TT: 98.4

10-year+ 10-year
Mazzaferri and Young [7]
N = 576
TL: 19.2 TL: 98.5
TT: 10.9 TT: 99.4

30-year+ 30-year
Hay et al. [8]
(N = 1685)
TL: 22.2 TL: 97.6
TT: 8.3 TT: 97.4

TT: total thyroidectomy, TL: thyroid lobectomy.

+Statistically significant (P ≤ 0.05).

Table 3.

Comparison of outcomes of by tumor size (cm).

Study Recurrence (%) Survival (%)
10-year+ 10-year
Mazzaferri and Young [7]
N = 576
<1.5 : 4.8 <1.5 : 100.0
≥1.5 : 12.7 ≥1.5 : 97.9

30-year+ 30-year
Mazzaferri and Jhiang [9]
N = 1355
<1.5 : 8 <1.5 : 100
1.5–4.4 : 31 1.5–4.4 : 94
≥4.5 : 36 ≥4.5 : 86

10-year+ 10-year
<1 : 4.6 <1 : 98.0
1–1.9 : 7.1 1–1.9 : 98.4
Bilimoria et al. [6]
N = 52,173
2–2.9 : 8.6 2–2.9 : 98.5
3–3.9 : 11.6 3–3.9 : 95.5
4–8 : 17.2 4–8+ : 90.5
>8 : 24.8 >8+ : 81.3

+Statistically significant (P ≤ 0.05).

Conventional open thyroid surgery, described initially by Dr. Emil Kocher [25], has been the standard surgical technique for almost a century. This initially involved a 8–10 cm transverse midline neck incision and, over the years, greatly reduced to standard a 3–6 cm incision [26]. Although this method is quick, provides excellent exposure, and leaves a scar hidden in the skin crease, the risk of scar hypertrophy and search for better cosmetic results have led to the development of minimally invasive techniques, such as video-assistance, endoscopy, and robotic surgery.

3.2.1. Endoscopic Thyroid Surgery

Endoscopic thyroid surgery was first described in 1997 by Huscher et al. [27] This technique, popularly known as minimally invasive video assisted thyroidectomy (MIVAT) is the most widely accepted endoscopic technique. Developed by Miccoli et al. [28] the video-assisted techniques are divided into three steps: the access to the thyroid bed and the creation of the working space through the minimal skin incision(s); the dissection of the thyroid lobe(s) after the identification of the recurrent laryngeal nerve and the parathyroid glands; and the retrieval of the thyroid lobe(s) and closure of the wounds. These three parts of the operation may last different lengths of time according to the different techniques used. Three main endoscopic approaches have been described for the thyroid gland: the cervical [29], the axillary [30], and the breast/lateral approach [31]. The safety of the video-assisted cervical approach has been established by Miccoli's series of 833 patients [32] and established by numerous reports, which have confirmed a similar complication rate compared to open thyroidectomy, as well as improved cosmesis and faster recovery (Table 4) [1014].

Table 4.

Comparison of outcomes of open, endoscopic and robot assisted thyroidectomy.

Study Surgery Size (cm) CND (%) Operative time (min) Complications (%)
Transient hypocalcemia Permanent hypocalcemia Transient RLN palsy Permanent RLN palsy Hematoma
Jong et al. [10] O (n = 224)
E (n = 275)
O: 0.60 ± 0.22
E: 0.56 ± 0.19
Prophylactic ipsilateral in all patients O: 105.5 ± 41.6
E: 138.5 ± 49.0
O: 17.1
E: 31.0
O: 1.7
E: 0.0
O: 2.2
E: 5.5
O: 0.4
E: 0.4
O: 0.9
E: 1.5

Di et al. [11] O (n = 37)
E (n = 31)
O: 0.73 ± 0.14
E: 0.76 ± 0.15
All patients underwent CND O: 105.4 ± 37.0
E: 143.9 ± 19.2
O: 2.7
E: 9.7
O: 0.0
E: 0.0
O: 5.4
E: 9.7
O: 0.0
E: 0.0
O: 0.0
E: 0.0

Kim et al. [12] O (n = 138)
E (n = 95)
R (n = 69)
O: 0.7 ± 0.2
E: 0.6 ± 0.2
R: 0.6 ± 0.2
Prophylactic ipsilateral in all patients O: 81 ± 16
E: 136 ± 31
R: 196 ± 45
O: 27.5
E: 25.3
R: 33.3
O: 0.0
E: 2.1
R: 0.0
O: 0.7
E: 2.1
R: 1.4
O: 0.0
E: 2.1
R: 0.0
O: 0.0
E: 1.1
R: 0.0

Lee et al. [13] E (n = 96)
R (n = 163)
E: 0.84 ± 0.41
R: 0.87± 0.64
E: 54.2
R: 91.4
E: 142.7 ± 52.1
R: 110.1 ± 50.7
E: 0.0
R: 12.5
E: 0.0
R: 0.0
E: 3.1
R: 1.8
E: 1.0
R: 0.6
E: 3.1
R: 0.6

Chung et al. [14] O (n = 198)
E (n = 103)
≤0.5 cm (%)
O: 52.0
E: 56.3
0.5–1 cm (%)
O: 48.0
E: 43.7
O: 8.1
E: 1.0
O: 111.4
E: 165.1
(S.D. not reported)
O: 17.7
E: 25.2
O: 4.5
E: 1.0
O: 2.5
E: 25.2
O: 0.5
E: 0.0
O: 0.0
E: 1.0

O: open thyroidectomy, E: endoscopic thyroidectomy, R: robot assisted thyroidectomy, CND: central lymph node dissection, S.D.: standard deviation, continuous variable reported as mean ± S.D., categorical variables reported as percentages (%).

3.2.2. Robotic Thyroid Surgery

In general, conventional endoscopic surgeries have some limitations in obtaining adequate visualizations and precise, meticulous manipulation of the surgical tissues. These limitations result from the two-dimensional representation and the simplicity of the endoscopic instruments used. The da Vinci S surgical robot system (Intuitive Surgical, Sunnyvale, CA, USA) was developed to address these limitations of conventional endoscopic surgery This procedure was initially described by Kang et al. [33] and avoids the use of a neck incision altogether. However, it has been shown that operative times are longer, and there is a significant learning curve for the procedure (Table 4) [34]. Additionally, it is subject to increased cost for the robot and potentially longer operative times, and some would argue that the procedure is more invasive due to the dissection needed to approach from the axilla across the chest to reach the thyroid.

3.3. Lymph Node Dissection: Prophylactic or Therapeutic?

Patients with DTC commonly have lymph node involvement. While up to 20–90% patients with PTC may have lymph node metastasis detected during the initial surgery, the rate of lymph node involvement is substantially lower (2%) with follicular thyroid cancer (FTC) [3537]. Although lymph node status is not a part of several staging systems, such as the AGES [38] and the AMES [4], it is used to stratify prognosis in patients older than 45 years with DTC according to the AJCC [39].

The central neck or level VI lymph node compartment is anatomically bounded by the hyoid bone superiorly, the innominate artery inferiorly, and the carotid sheath laterally [40]. Since the recurrent laryngeal nerves and the parathyroid glands are situated in this compartment, careful surgical dissection is required to preserve function of these structures.

It is universally accepted that a therapeutic CND should be performed; metastatic lymph nodes are identified on physical exam, ultrasound, or intraoperatively [23]. Therapeutic lymph node dissection decreases the incidence of locoregional recurrence (by up to 2–7%), prevent local progression into adjacent structures, and improve survival (by up to 3–9%) [36, 41, 42].

In the absence of overt nodal metastasis, the role of elective prophylactic central lymph node dissection remains a matter of debate [41, 43]. Unanticipated microscopic metastases are identified in 38–45% patients undergoing prophylactic CND [19, 44]. However, preoperative radiologic evaluation of the central compartment is limited by the overlying thyroid gland. Furthermore, intraoperative inspection is highly inaccurate in identifying lymph node involvement [45, 46].

The American Thyroid Association (ATA) guidelines recommend performing prophylactic CND in patients with PTC and locally advanced primary tumors (T3 and T4) [23]. This recommendation is based on evidence from retrospective studies [47, 48]. Scheumann et al. had reported decreased recurrence (P < 0.00001) and improved survival (P = 0.005) in 342 patients with T1–T3 disease who had total thyroidectomy with CND as compared to total thyroidectomy alone [47]. The ATA guidelines recommend thyroidectomy without prophylactic CND for small (T1 and T2), noninvasive and clinically node negative PTC and most FTC. Patients meeting these criteria have a lower risk of lymph node metastasis and are less likely to benefit from additional surgery. The European Thyroid Cancer Taskforce also recommends prophylactic CND only in patients with preoperatively suspected and/or intraoperatively proven lymph node metastasis [47]. A recent systematic review and meta-analysis of 16 retrospective studies by Shan et al. [49] reported no difference in recurrence rates, rate of recurrent laryngeal nerve injuries (temporary or permanent), or permanent hypocalcemia between total thyroidectomy with CND as compared to total thyroidectomy alone. Temporary hypocalcemia was seen to be more common in the CND group (Table 5) [1519]. In the light of these conflicting reports, the role of prophylactic CND is still a topic of considerable debate and larger prospective trials are needed to evaluate the benefit of prophylactic CND in DTC.

Table 5.

Comparison of outcomes of total thyroidectomy with or without central lymph node dissection.

Study RLN Injury (%) Hypocalcemia (%) Recurrence (%)
Temporary Permanent Temporary Permanent
Shen et al. [15] TT: 3.7 TT: 1.0 TT: 11.0 TT: 0 TT: 21.8
(N = 301) TT + CND: 1.8 TT + CND: 1.8 TT + CND: 38.2 TT + CND: 0 TT + CND: 5.7

Moo et al. [16] TT: 0 TT: 0 TT: 5.6 TT: 5.5 TT: 16.7
(N = 81) TT + CND: 4.4 TT + CND: 0 TT + CND: 31.1 TT + CND: 0 TT + CND: 4.4

Rosenbaum McHenry [17] TT: 2.3 TT: 1.1 TT: 57.9 TT: 0 TT: 4.5
(N = 110) TT + CND: 9.1 TT + CND: 0 TT + CND: 86.4 TT + CND: 4.5 TT + CND: 2.3

Perrino et al. [18] TT: 3.1 TT: 2.5 TT: 6.9 TT: 3.8 TT: 13.8
(N = 251) TT + CND: 2.2 TT + CND: 1.1 TT + CND: 8.7 TT + CND: 1.1 TT + CND: 5.4

Sywak et al. [19] TT: 1.0 TT: 1.0 TT: 8.2 TT: 0.5 TT: 5.6
(N = 447) TT + CND: 1.8 TT + CND: 0 TT + CND: 17.8 TT + CND: 1.8 TT + CND: 3.6

TT: total thyroidectomy alone, TT + CND: total thyroidectomy with central lymph node dissection.

Thyroid cancer can also metastasize to the lateral compartment of lymph nodes comprising of levels II–V. Suspicious lymph nodes in the lateral compartment [40] should be biopsied by FNA, and if positive, a modified radical lymphadenectomy should be performed. Studies have shown that cytoreductive surgery is associated with decreased recurrence and improved survival [45, 50, 51], however an en block resection can be associated with significant morbidity, including long-term motor dysfunction. Thus in patients with minimal disease, a limited lymphadenectomy is desirable. Nodal metastasis is most commonly found in level III, followed by levels IV and II, with level V being least common [52, 53]. Therefore, it is well accepted to perform a targeted compartmental lymph node dissection, aided by preoperative assessment, while “berry picking” or isolated lymphadenectomy is discouraged.

Patients at risk for developing aggressive disease can be identified using molecular testing for gene alterations present in PTC, such as BRAF and RAS as well as RET-PTC and PAX8-PPARG rearrangements [5456]. Such patients could derive increased benefit from prophylactic CND [54, 56]. Although the utility of molecular testing has not yet been prospectively evaluated in randomized trails, testing for BRAF, which is the best studied thyroid oncogene, is routinely performed in some institutions to guide decision making in patients with PTC [57].

4. Conclusion

DTC has become an increasingly common malignancy. It is well accepted that surgery remains the mainstay of treatment of this disease and there have been tremendous advances in the approach to surgery over the last two decades. MIVAT and robotic thyroidectomy are seen to be safe and effective approaches in the hands of the trained surgeon and in selected patient populations. However, there is still considerable debate regarding the role of prophylactic lymph node dissection in the absence of preoperative or intraoperative signs of nodal metastasis. Randomized and prospective studies are warranted to shed more light on the indications for this procedure.

References

  • 1.Kebebew E, Clark OH. Differentiated thyroid cancer: “complete” rational approach. World Journal of Surgery. 2000;24(8):942–951. doi: 10.1007/s002680010165. [DOI] [PubMed] [Google Scholar]
  • 2.Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer Journal for Clinicians. 2011;61(2):69–90. doi: 10.3322/caac.20107. [DOI] [PubMed] [Google Scholar]
  • 3.Shaha AR. Implications of prognostic factors and risk groups in the management of differentiated thyroid cancer. Laryngoscope. 2004;114(3):393–402. doi: 10.1097/00005537-200403000-00001. [DOI] [PubMed] [Google Scholar]
  • 4.Cady B. Our AMES is true: how an old concept still hits the mark: or, risk group assignment points the arrow to rational therapy selection in differentiated thyroid cancer. American Journal of Surgery. 1997;174(5):462–468. doi: 10.1016/s0002-9610(97)00162-1. [DOI] [PubMed] [Google Scholar]
  • 5.Tuttle RM, Leboeuf R, Shaha AR. Medical management of thyroid cancer: a risk adapted approach. Journal of Surgical Oncology. 2008;97(8):712–716. doi: 10.1002/jso.21010. [DOI] [PubMed] [Google Scholar]
  • 6.Bilimoria KY, Bentrem DJ, Ko CY, et al. Extent of surgery affects survival for papillary thyroid cancer. Annals of Surgery. 2007;246(3):375–384. doi: 10.1097/SLA.0b013e31814697d9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Mazzaferri EL, Young RL. Papillary thyroid carcinoma: a 10 year follow-up report of the impact of therapy in 576 patients. American Journal of Medicine. 1981;70(3):511–518. doi: 10.1016/0002-9343(81)90573-8. [DOI] [PubMed] [Google Scholar]
  • 8.Hay ID, Thompson GB, Grant CS, et al. Papillary thyroid carcinoma managed at the Mayo Clinic during six decades (1940–1999): temporal trends in initial therapy and long-term outcome in 2444 consecutively treated patients. World Journal of Surgery. 2002;26(8):879–885. doi: 10.1007/s00268-002-6612-1. [DOI] [PubMed] [Google Scholar]
  • 9.Mazzaferri EL, Jhiang SM. Long-term impact of initial surgical and medical therapy on papillary and follicular thyroid cancer. American Journal of Medicine. 1994;97(5):418–428. doi: 10.1016/0002-9343(94)90321-2. [DOI] [PubMed] [Google Scholar]
  • 10.Jong JJ, Kang SW, Yun JS, et al. Comparative study of endoscopic thyroidectomy versus conventional open thyroidectomy in papillary thyroid microcarcinoma (PTMC) patients. Journal of Surgical Oncology. 2009;100(6):477–480. doi: 10.1002/jso.21367. [DOI] [PubMed] [Google Scholar]
  • 11.Di JZ, Zhang HW, Han XD, et al. Minimally invasive video-assisted thyroidectomy for accidental papillary thyroid microcarcinoma: comparison with conventional open thyroidectomy with 5 years follow-up. Chinese Medical Journal. 2011;124:3293–3296. [PubMed] [Google Scholar]
  • 12.Kim WW, Kim JS, Hur SM, et al. Is robotic surgery superior to endoscopic and open surgeries in thyroid cancer? World Journal of Surgery. 2011;35(4):779–784. doi: 10.1007/s00268-011-0960-7. [DOI] [PubMed] [Google Scholar]
  • 13.Lee J, Lee JH, Nah KY, Soh EY, Chung WY. Comparison of endoscopic and robotic thyroidectomy. Annals of Surgical Oncology. 2011;18(5):1439–1446. doi: 10.1245/s10434-010-1486-1. [DOI] [PubMed] [Google Scholar]
  • 14.Chung YS, Choe JH, Kang KH, et al. Endoscopic thyroidectomy for thyroid malignancies: comparison with conventional open thyroidectomy. World Journal of Surgery. 2007;31(12):2302–2308. doi: 10.1007/s00268-007-9117-0. [DOI] [PubMed] [Google Scholar]
  • 15.Shen WT, Ogawa L, Ruan D, Suh I, Duh QY, Clark OH. Central neck lymph node dissection for papillary thyroid cancer: the reliability of surgeon judgment in predicting which patients will benefit. Surgery. 2010;148(2):398–403. doi: 10.1016/j.surg.2010.03.021. [DOI] [PubMed] [Google Scholar]
  • 16.Moo TA, McGill J, Allendorf J, Lee J, Fahey T, Zarnegar R. Impact of prophylactic central neck lymph node dissection on early recurrence in papillary thyroid carcinoma. World Journal of Surgery. 2010;34(6):1187–1191. doi: 10.1007/s00268-010-0418-3. [DOI] [PubMed] [Google Scholar]
  • 17.Rosenbaum MA, McHenry CR. Central neck dissection for papillary thyroid cancer. Archives of Otolaryngology. 2009;135(11):1092–1097. doi: 10.1001/archoto.2009.158. [DOI] [PubMed] [Google Scholar]
  • 18.Perrino M, Vannucchi G, Vicentini L, et al. Outcome predictors and impact of central node dissection and radiometabolic treatments in papillary thyroid cancers ≤2 cm. Endocrine-Related Cancer. 2009;16(1):201–210. doi: 10.1677/ERC-08-0119. [DOI] [PubMed] [Google Scholar]
  • 19.Sywak M, Cornford L, Roach P, Stalberg P, Sidhu S, Delbridge L. Routine ipsilateral level VI lymphadenectomy reduces postoperative thyroglobulin levels in papillary thyroid cancer. Surgery. 2006;140(6):1000–1007. doi: 10.1016/j.surg.2006.08.001. [DOI] [PubMed] [Google Scholar]
  • 20.Hawk WA, Hazard JB. The many appearances of papillary carcinoma of the thyroid. Cleveland Clinic Quarterly. 1976;43(4):207–215. doi: 10.3949/ccjm.43.4.207. [DOI] [PubMed] [Google Scholar]
  • 21.Michels JJ, Jacques M, Henry-Amar M, Bardet S. Prevalence and prognostic significance of tall cell variant of papillary thyroid carcinoma. Human Pathology. 2007;38(2):212–219. doi: 10.1016/j.humpath.2006.08.001. [DOI] [PubMed] [Google Scholar]
  • 22.Leung AKC, Chow SM, Law SCK. Clinical features and outcome of the tall cell variant of papillary thyroid carcinoma. Laryngoscope. 2008;118(1):32–38. doi: 10.1097/MLG.0b013e318156f6c3. [DOI] [PubMed] [Google Scholar]
  • 23.Cooper DS, Doherty GM, Haugen BR, et al. Revised American thyroid association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid. 2009;19(11):1167–1214. doi: 10.1089/thy.2009.0110. [DOI] [PubMed] [Google Scholar]
  • 24.Shaha AR, Shah JP, Loree TR. Low-risk differentiated thyroid cancer: the need for selective treatment. Annals of Surgical Oncology. 1997;4(4):328–333. doi: 10.1007/BF02303583. [DOI] [PubMed] [Google Scholar]
  • 25.Morris JB, Schirmer WJ. The “right stuff”: five nobel prize-winning surgeons. Surgery. 1990;108(1):71–80. [PubMed] [Google Scholar]
  • 26.Brunaud L, Zarnegar R, Wada N, Ituarte P, Clark OH, Duh QY. Incision length for standard thyroidectomy and parathyroidectomy: when is it minimally invasive? Archives of Surgery. 2003;138(10):1140–1143. doi: 10.1001/archsurg.138.10.1140. [DOI] [PubMed] [Google Scholar]
  • 27.Huscher CS, Chiodini S, Napolitano C, Recher A. Endoscopic right thyroid lobectomy. Surgical Endoscopy. 1997;11, article 877 doi: 10.1007/s004649900476. [DOI] [PubMed] [Google Scholar]
  • 28.Miccoli P, Berti P, Bendinelli C, Conte M, Fasolini F, Martino E. Minimally invasive video-assisted surgery of the thyroid: a preliminary report. Langenbeck’s Archives of Surgery. 2000;385(4):261–264. doi: 10.1007/s004230000141. [DOI] [PubMed] [Google Scholar]
  • 29.Inabnet WB, III, Jacob BP, Gagner M. Minimally invasive endoscopic thyroidectomy by a cervical approach: early vessel ligation decreases the duration of surgery. Surgical Endoscopy and Other Interventional Techniques. 2003;17(11):1808–1811. doi: 10.1007/s00464-002-8760-7. [DOI] [PubMed] [Google Scholar]
  • 30.Ikeda Y, Takami H, Sasaki Y, Kan S, Niimi M. Endoscopic neck surgery by the axillary approach. Journal of the American College of Surgeons. 2000;191(3):336–340. doi: 10.1016/s1072-7515(00)00342-2. [DOI] [PubMed] [Google Scholar]
  • 31.Palazzo FF, Sebag F, Henry JF. Endocrine surgical technique: endoscopic thyroidectomy via the lateral approach. Surgical Endoscopy and Other Interventional Techniques. 2006;20(2):339–342. doi: 10.1007/s00464-005-0385-1. [DOI] [PubMed] [Google Scholar]
  • 32.Miccoli P, Berti P, Frustaci GL, Ambrosini CE, Materazzi G. Video-assisted thyroidectomy: indications and results. Langenbeck’s Archives of Surgery. 2006;391(2):68–71. doi: 10.1007/s00423-006-0027-7. [DOI] [PubMed] [Google Scholar]
  • 33.Kang SW, Lee SC, Lee SH, et al. Robotic thyroid surgery using a gasless, transaxillary approach and the da Vinci S system: the operative outcomes of 338 consecutive patients. Surgery. 2009;146(6):1048–1055. doi: 10.1016/j.surg.2009.09.007. [DOI] [PubMed] [Google Scholar]
  • 34.Kuppersmith RB, Holsinger FC. Robotic thyroid surgery: an initial experience with North American patients. Laryngoscope. 2011;121(3):521–526. doi: 10.1002/lary.21347. [DOI] [PubMed] [Google Scholar]
  • 35.Fritze D, Doherty GM. Surgical management of cervical lymph nodes in differentiated thyroid cancer. Otolaryngologic Clinics of North America. 2010;43(2):285–300. doi: 10.1016/j.otc.2010.01.005. [DOI] [PubMed] [Google Scholar]
  • 36.Bardet S, Malville E, Rame JP, et al. Macroscopic lymph-node involvement and neck dissection predict lymph-node recurrence in papillary thyroid carcinoma. European Journal of Endocrinology. 2008;158(4):551–560. doi: 10.1530/EJE-07-0603. [DOI] [PubMed] [Google Scholar]
  • 37.Arturi F, Russo D, Giuffrida D, et al. Early diagnosis by genetic analysis of differentiated thyroid cancer metastases in small lymph nodes. Journal of Clinical Endocrinology and Metabolism. 1997;82(5):1638–1641. doi: 10.1210/jcem.82.5.4062. [DOI] [PubMed] [Google Scholar]
  • 38.Hay ID, Grant CS, Taylor WF, McConahey WM. Ipsilateral lobectomy versus bilateral lobar resection in papillary thyroid carcinoma: a retrospective analysis of surgical outcome using a novel prognostic scoring system. Surgery. 1987;102(6):1088–1095. [PubMed] [Google Scholar]
  • 39.Brierley JD, Panzarella T, Tsang RW, et al. A comparison of different staging systems predictability of patient outcome. Thyroid carcinoma as an example. Cancer. 1997;79:2414–2423. [PubMed] [Google Scholar]
  • 40.Carty SE, Cooper DS, Doherty GM, et al. Consensus statement on the terminology and classification of central neck dissection for thyroid cancer. Thyroid. 2009;19(11):1153–1158. doi: 10.1089/thy.2009.0159. [DOI] [PubMed] [Google Scholar]
  • 41.Mazzaferri EL, Doherty GM, Steward DL. The pros and cons of prophylactic central compartment lymph node dissection for papillary thyroid carcinoma. Thyroid. 2009;19(7):683–689. doi: 10.1089/thy.2009.1578. [DOI] [PubMed] [Google Scholar]
  • 42.Zaydfudim V, Feurer ID, Griffin MR, Phay JE. The impact of lymph node involvement on survival in patients with papillary and follicular thyroid carcinoma. Surgery. 2008;144(6):1070–1078. doi: 10.1016/j.surg.2008.08.034. [DOI] [PubMed] [Google Scholar]
  • 43.Mazzaferri EL. What is the optimal initial treatment of low-risk papillary thyroid cancer (and why is it controversial)? Oncology. 2009;23(7):579–588. [PubMed] [Google Scholar]
  • 44.Pereira JA, Jimeno J, Miquel J, et al. Nodal yield, morbidity, and recurrence after central neck dissection for papillary thyroid carcinoma. Surgery. 2005;138(6):1095–1101. doi: 10.1016/j.surg.2005.09.013. [DOI] [PubMed] [Google Scholar]
  • 45.Kouvaraki MA, Shapiro SE, Fornage BD, et al. Role of preoperative ultrasonography in the surgical management of patients with thyroid cancer. Surgery. 2003;134(6):946–954. doi: 10.1016/s0039-6060(03)00424-0. [DOI] [PubMed] [Google Scholar]
  • 46.Moley JF, DeBenedetti MK. Patterns of nodal metastases in palpable medullary thyroid carcinoma: recommendations for extent of node dissection. Annals of Surgery. 1999;229(6):880–888. doi: 10.1097/00000658-199906000-00016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Scheumann GFW, Gimm O, Wegener G, Hundeshagen H, Dralle H, Cady B. Prognostic significance and surgical management of locoregional lymph node metastases in papillary thyroid cancer. World Journal of Surgery. 1994;18(4):559–568. doi: 10.1007/BF00353765. [DOI] [PubMed] [Google Scholar]
  • 48.Tisell LE, Nilsson B, Mölne J, et al. Improved survival of patients with papillary thyroid cancer after surgical microdissection. World Journal of Surgery. 1996;20(7):854–859. doi: 10.1007/s002689900130. [DOI] [PubMed] [Google Scholar]
  • 49.Shan CX, Zhang W, Jiang DZ, et al. Routine central neck dissection in differentiated thyroid carcinoma: a systematic review and meta-analysis. Laryngoscope. 2012;122:797–804. doi: 10.1002/lary.22162. [DOI] [PubMed] [Google Scholar]
  • 50.Gemsenjäger E, Perren A, Seifert B, Schüler G, Schweizer I, Heitz PU. Lymph node surgery in papillary thyroid carcinoma. Journal of the American College of Surgeons. 2003;197(2):182–190. doi: 10.1016/S1072-7515(03)00421-6. [DOI] [PubMed] [Google Scholar]
  • 51.Ito Y, Tomoda C, Uruno T, et al. Preoperative ultrasonographic examination for lymph node metastasis: usefulness when designing lymph node dissection for papillary microcarcinoma of the thyroid. World Journal of Surgery. 2004;28(5):498–501. doi: 10.1007/s00268-004-7192-z. [DOI] [PubMed] [Google Scholar]
  • 52.Kupferman ME, Patterson M, Mandel SJ, LiVolsi V, Weber RS. Patterns of lateral neck metastasis in papillary thyroid carcinoma. Archives of Otolaryngology. 2004;130(7):857–860. doi: 10.1001/archotol.130.7.857. [DOI] [PubMed] [Google Scholar]
  • 53.Caron NR, Tan YY, Ogilvie JB, et al. Selective modified radical neck dissection for papillary thyroid cancer—is level I, II and V dissection always necessary? World Journal of Surgery. 2006;30(5):833–840. doi: 10.1007/s00268-005-0358-5. [DOI] [PubMed] [Google Scholar]
  • 54.Xing M. Prognostic utility of BRAF mutation in papillary thyroid cancer. Molecular and Cellular Endocrinology. 2010;321(1):86–93. doi: 10.1016/j.mce.2009.10.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Nikiforov YE. Molecular analysis of thyroid tumors. Modern Pathology. 2011;242(supplement 2):S34–S43. doi: 10.1038/modpathol.2010.167. [DOI] [PubMed] [Google Scholar]
  • 56.Nikiforov YE, Nikiforova MN. Molecular genetics and diagnosis of thyroid cancer. Nature Reviews Endocrinology. 2011;7:569–580. doi: 10.1038/nrendo.2011.142. [DOI] [PubMed] [Google Scholar]
  • 57.Melck AL, Yip L, Carty SE. The utility of BRAF testing in the management of papillary thyroid cancer. Oncologist. 2010;15(12):1285–1293. doi: 10.1634/theoncologist.2010-0156. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Scientific World Journal are provided here courtesy of Wiley

RESOURCES