何杰,李新?tīng)I(yíng),王志明,張超杰,李勁東
甲狀腺乳頭狀癌是頭頸部外科最常見(jiàn)的惡性腫瘤之一,近年來(lái)發(fā)病率呈逐年上升的趨勢(shì),現(xiàn)約占甲狀腺癌的85%左右[1]。甲狀腺微小乳頭狀癌(papillary thyroid microcarcinoma,PTMC)是指最大直徑≤1 cm的腫瘤,一般認(rèn)為具有較低侵襲性和淋巴結(jié)轉(zhuǎn)移率,其術(shù)后生存率亦較非PTMC更好[2]。多灶性甲狀腺乳頭狀癌(multifocal papillary thyroid carcinoma,MPTC)是指病灶數(shù)目≥ 2個(gè)的甲狀腺乳頭狀癌,是甲狀腺癌的重要臨床特點(diǎn)之一[3]。目前多灶性PTMC是甲狀腺外科醫(yī)生需要面對(duì)的重要課題之一,其臨床病理特征、治療和預(yù)后尚缺乏深入的研究。中南大學(xué)湘雅醫(yī)院2013年7月—2016年12月共收治270例PTMC,其中120例為多灶性PTMC。本文回顧性分析120例多灶性PTMC的臨床資料,探討多灶PTMC的臨床特點(diǎn)和預(yù)防性中央?yún)^(qū)淋巴結(jié)清掃的意義。
將2013年7月—2016年12月收治的270例PTMC患者中120例多灶PTMC的臨床資料和手術(shù)結(jié)果分析研究。納入研究的患者均為初次發(fā)病者,患者既往無(wú)頸部手術(shù)、甲狀腺消融及外傷史。所有患者術(shù)前均行彩色超聲評(píng)估甲狀腺結(jié)節(jié),基于患者意愿和臨床因素,術(shù)前對(duì)影像學(xué)懷疑惡性,腫瘤直徑≥5 mm的病灶行細(xì)針穿刺活檢(fine needle aspiration biopsy,F(xiàn)NAB)結(jié)果顯示為可疑惡性或惡性。觸診和彩超評(píng)估頸部淋巴結(jié)無(wú)術(shù)前轉(zhuǎn)移淋巴結(jié)征象。所有患者經(jīng)術(shù)后石蠟切片證實(shí)甲狀腺內(nèi)有2個(gè)或2個(gè)以上的病灶,其中病灶最大直徑<1 cm。14例患者術(shù)前各項(xiàng)評(píng)估考慮為單發(fā)病灶,但經(jīng)術(shù)中冷凍切片和術(shù)后石蠟切片確診為多灶PTMC。
所有患者均行全/近全甲狀腺切除,術(shù)中冷凍切片證實(shí)為多灶性甲狀腺微小乳頭狀癌。全部病灶位于一側(cè)甲狀腺腺葉者行患側(cè)中央?yún)^(qū)淋巴結(jié)清掃,病灶分布于雙側(cè)腺葉者則行雙側(cè)中央?yún)^(qū)淋巴結(jié)清掃術(shù)。術(shù)中全程暴露喉返神經(jīng)并加以保護(hù);原位保留甲狀旁腺,必要時(shí)行甲狀旁腺自體移植。中央?yún)^(qū)淋巴結(jié)清掃包括喉前、氣管前、氣管旁和氣管食管溝的淋巴脂肪,右側(cè)中央?yún)^(qū)注意清掃喉返神經(jīng)后方淋巴脂肪組織。
統(tǒng)計(jì)和比較全部納入研究的患者年齡,性別,原發(fā)腫瘤直徑、數(shù)目,是否分布于雙側(cè),是否侵犯包膜,有無(wú)中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移和轉(zhuǎn)移情況等臨床病理特征。比較分析多灶性PTMC和單灶性PTMC的臨床病理特征,研究影響中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移的因素。
采用SPSS 16.5軟件對(duì)兩組所得的數(shù)據(jù)進(jìn)行統(tǒng)計(jì)分析,一般資料用均數(shù)±標(biāo)準(zhǔn)差(±s)的形式表示。計(jì)量資料采用t檢驗(yàn),計(jì)數(shù)資料比較采用χ2檢驗(yàn),P<0.05 為差異有統(tǒng)計(jì)學(xué)意義。
本組120例患者中男33例,女87例;年齡23~68歲,平均年齡(44.23±10.59)歲;腫瘤直徑1~10 mm,平均直徑(4.90±1.67)mm;病灶位于甲狀腺單側(cè)腺葉者38例(31.67%),位于雙側(cè)腺葉者82例(68.33%);30例(25.0%)經(jīng)術(shù)后病理證實(shí)腫瘤侵犯甲狀腺包膜。術(shù)前臨床考慮為單灶,術(shù)中、術(shù)后病理證實(shí)為多灶的14例(11.67%)。38例(31.67%)患者存在中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移,其中雙側(cè)轉(zhuǎn)移24例(20.0%),單側(cè)轉(zhuǎn)移14例(11.67%)。多灶性與單灶性PTMC在發(fā)病年齡、單個(gè)腫瘤直徑上無(wú)統(tǒng)計(jì)學(xué)差異(P>0.05);與單灶性PTMC相比,多灶性PTMC在男性患者中比例較高、更容易出現(xiàn)包膜侵犯(均P<0.05),且更容易發(fā)生中央?yún)^(qū)淋巴結(jié)的轉(zhuǎn)移(P<0.01)(表1)。
表1 多灶PTMC與單灶PTMC患者臨床資料比較Table 1 Comparison of the clinical data between multifocal and unifocal PTMC patients
分析臨床病理因素包括年齡、性別、腫瘤最大直徑、病灶數(shù)目、病灶分布和是否侵犯甲狀腺包膜與中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移的關(guān)系。結(jié)果顯示:中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移的發(fā)生與患者年齡和性別無(wú)關(guān)(均P>0.05);腫瘤最大直徑5~10 mm者較<5 mm者中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率明顯升高(P<0.05);腫瘤侵犯包膜者更容易出現(xiàn)中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移(P<0.05);多灶PTMC腫瘤數(shù)目(2vs.≥3)和分布(單側(cè)vs.雙側(cè))與中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率無(wú)關(guān)(均P>0.05)(表2)。
表2 多灶PTMC患者臨床因素與中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移關(guān)系[n(%)]Table 2 Relations of clinical factors with central lymph node metastasis in multifocal PTMC patients [n (%)]
120例患者術(shù)后并發(fā)癥發(fā)生6例。術(shù)后暫時(shí)性低鈣血癥3例(2.5%),1個(gè)月后復(fù)查血鈣和PTH均恢復(fù)正常。暫時(shí)性聲帶麻痹2例(1.67%),3個(gè)月后復(fù)查聲帶活動(dòng)和發(fā)音均恢復(fù)正常。術(shù)后皮下出血1例(0.83%),經(jīng)局部壓迫及切口處引流后好轉(zhuǎn)。無(wú)永久性喉返神經(jīng)麻痹和永久性甲狀旁腺功能低下,無(wú)死亡病例。
近年來(lái)甲狀腺乳頭狀癌發(fā)病率的迅速上升,其中有約50%以上歸因于甲狀腺微小乳頭狀癌(PTMC)的增長(zhǎng)[4-5]。臨床上PTMC具有較低的術(shù)后復(fù)發(fā)率約1%~5%,如果僅統(tǒng)計(jì)CN0期患者則其復(fù)發(fā)率低至1%以下[6-7]?;赑TMC惰性的生物學(xué)行為和良好的預(yù)后,甚至有研究[8-10]提出對(duì)低危PTMC患者可以進(jìn)行嚴(yán)密的動(dòng)態(tài)監(jiān)測(cè)。多灶性作為甲狀腺乳頭狀癌的重要臨床特征,根據(jù)不同的報(bào)道其發(fā)病率約為18%~87%[11]。研究[12]表明多發(fā)病灶具有較高的包膜侵犯率和淋巴轉(zhuǎn)移發(fā)生率,其是甲狀腺乳頭狀癌殘存和復(fù)發(fā)的獨(dú)立高風(fēng)險(xiǎn)因素。因此,多灶PTMC臨床病理的特點(diǎn)和對(duì)其手術(shù)方式的選擇逐漸成為研究的熱點(diǎn)之一。
多灶性PTMC兼具甲狀腺乳頭狀微小癌和多灶性的臨床特性,越來(lái)越多地引起外科醫(yī)生的關(guān)注。So等[13]報(bào)道多灶性甲狀腺微小乳頭狀癌的發(fā)生率為36.1%。本組患者中多灶性PTMC 44.4%(120/270),略高于文獻(xiàn)報(bào)道。多數(shù)研究[11,14]顯示多灶與單灶甲狀腺乳頭狀癌中性別比例和年齡比較沒(méi)有差異。本組結(jié)果顯示多灶組PTMC中男性的發(fā)病率要高于單灶組PTMC(27.5%vs.16.0%,P=0.021);而兩者在年齡上則無(wú)統(tǒng)計(jì)學(xué)差異,這與單志東等[15]研究結(jié)果一致。研究[16]顯示多灶PTMC的腫瘤平均直徑明顯小于單灶PTMC的腫瘤直徑,而將多灶PTMC分成2個(gè)和≥3個(gè)病灶組是則無(wú)顯著差異。本組結(jié)果顯示多灶組的腫瘤平均直徑小于單灶組,但兩者無(wú)統(tǒng)計(jì)學(xué)差異(P=0.301)。多灶PTMC位于雙側(cè)腺葉的比率為69.6%,而且單側(cè)多發(fā)PTMC比單側(cè)單發(fā)PTMC對(duì)側(cè)微小癌的發(fā)生率會(huì)成倍增加(69.1%vs.29.6%)[17-19]。本組多灶性PTMC位于雙側(cè)者占68.3%,與上述研究結(jié)果一致。有報(bào)道[20]稱5.5%~21.3%的多灶PTMC患者存在常規(guī)術(shù)前B超檢查和穿刺細(xì)胞學(xué)活檢未能發(fā)現(xiàn)的隱匿病灶,這是造成術(shù)后的漏診和復(fù)發(fā)的主要因素。本組亦有14例術(shù)前臨床考慮為單灶,術(shù)后病理確診為多灶。說(shuō)明多灶PTMC中常合并存在一些極其微小不易被發(fā)現(xiàn)的潛在病灶,可以局限一側(cè)腺葉,也可以位于兩側(cè)。包膜侵犯是甲狀腺乳頭狀癌淋巴結(jié)轉(zhuǎn)移和預(yù)后風(fēng)險(xiǎn)因素之一,在多灶性PTMC的發(fā)生率顯著高于單灶性PTMC[9,11,19]。Kim等[12]研究多灶性PTMC的中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率為42.1%,明顯高于單灶性(28.1%)。本組資料顯示多灶性PTMC的包膜侵犯和中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率均顯著高于單灶組PTMC,與前述研究結(jié)果一致。
中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移是甲狀腺癌的主要轉(zhuǎn)移途徑之一,同時(shí)也是復(fù)發(fā)和遠(yuǎn)處轉(zhuǎn)移的危險(xiǎn)因素之一[21-22]。C N0期P T M C中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率約3 3%左右,而多灶P T M C頸淋巴結(jié)轉(zhuǎn)移率則可高達(dá)5 5.6%[23-24]。本組數(shù)據(jù)顯示對(duì)于C N0的患者進(jìn)行預(yù)防性中央?yún)^(qū)淋巴結(jié)清掃,淋巴結(jié)轉(zhuǎn)移發(fā)生率(3 8/1 2 0,3 1.7%)。Z h a n g等[25]研究顯示P T M C的中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移與男性、年齡(≤4 5歲)、多灶性、腺外侵犯和大?。ǎ? m m)密切相關(guān)。而目前多項(xiàng)研究建議將分期中的年齡切點(diǎn)值由45歲增至55歲[26-27],美國(guó)癌癥聯(lián)合委員會(huì)(American Joint Committee on Cancer AJCC)最新甲狀腺癌分期也已將年齡界限更改為55歲,因此我們分析性別及年齡(55歲為界限)對(duì)中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移的影響,未見(jiàn)明顯差異(P>0.05)。通常認(rèn)為直徑越大的腫瘤發(fā)生淋巴結(jié)轉(zhuǎn)移的風(fēng)險(xiǎn)越大,本研究在對(duì)5~10 mm與<5 mm的病灶對(duì)比中發(fā)現(xiàn),5~10 mm的病灶發(fā)生中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移風(fēng)險(xiǎn)更高(P=0.032)。也有部分學(xué)者[28]把這個(gè)臨界值定在7mm,認(rèn)為<5 mm與5~7 mm之間病灶比較中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移無(wú)明顯差異。Tam等[14]研究顯示隨病灶數(shù)目的增加淋巴結(jié)轉(zhuǎn)移發(fā)生率亦逐漸升高,病灶數(shù)為1、2、3和4個(gè)的淋巴結(jié)轉(zhuǎn)移發(fā)生率分別為6.5%、10.5%、13.6%和19.2%。本組比較病灶的數(shù)目(2vs.≥3)和分布(單側(cè)vs.雙側(cè))與中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率的關(guān)系,結(jié)果顯示沒(méi)有差異,這可能與病例分組和例數(shù)有關(guān)。本組結(jié)果顯示包膜侵犯明顯增加中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移發(fā)生率(P<0.05),這與大多數(shù)研究[11,13-14,25]結(jié)果一致。多數(shù)研究[29-30]證實(shí)中央?yún)^(qū)淋巴結(jié)清掃并不增加永久性甲狀旁腺功能低下和永久性聲帶麻痹。本組術(shù)后并發(fā)癥例數(shù)6例(5%)包括3例術(shù)后暫時(shí)性低鈣血癥(2.5%)和2例暫時(shí)性聲帶麻痹(1.67%),無(wú)永久性喉返神經(jīng)麻痹和永久性甲狀旁腺功能低下。
綜上所述,多灶性PTMC與單灶性PTMC相比包膜侵犯和中央?yún)^(qū)淋巴結(jié)轉(zhuǎn)移的發(fā)生率更高。多灶PTMC行預(yù)防性中央?yún)^(qū)淋巴結(jié)清掃術(shù)是很有必要的,尤其是最大腫瘤直徑>5mm和出現(xiàn)包膜侵犯者。
[1]Yin DT, Xu J, Lei M, et al. Characterization of the novel tumorsuppressor gene CCDC67 in papillary thyroid carcinoma [J].Oncotarget, 2016, 7(5):5830–5841. doi: 10.18632/oncotarget.6709.
[2]Lo CY,Chan WF, Lang BH, et al. Papillary microcarcinoma: is there any difference between clinically overt and occult tumors?[J].World J Surg, 2006, 30(5):759–766.
[3]Wang W, Su X, He K, et al. Comparison of the clinicopathologic features and prognosis of bilateral versus unilateral multifocal papillary thyroid cancer: An updated study with more than 2000 consecutive patients[J]. Cancer, 2016, 122(2):198–206. doi:10.1002/cncr.29689.
[4]Enewold LR, Zhou J, Devesa SS, et al. Thyroid cancer incidence among active duty U.S. military personnel, 1990–2004[J]. Cancer Epidemiol Biomarkers Prev, 2011, 20(11):2369–2376. doi:10.1158/1055–9965.EPI-11–0596.
[5]Davies L, Welch HG. Increasing incidence of thyroid cancer in the United States, 1973–2002[J]. JAMA, 2006, 295(18):2164–2167.
[6]Leboulleux S, Tuttle RM, Pacini F, et al. Papillary thyroid microcarcinoma: time to shift from surgery to active surveillance?[J]. Lancet Diabetes Endocrinol, 2016, 4(11):933–942.doi: 10.1016/S2213–8587(16)30180–2.
[7]Wada N, Duh QY, Sugino K,et al. Lymph node metastasis from 259 papillary thyroid microcarcinomas: frequency, pattern of occurrence and recurrence, and optimal strategy for neck dissection[J]. Ann Surg, 2003, 237(3):399–407. Epub 2003/03/05.
[8]Haser GC, Tuttle RM, Su HK, et al. Active Surveillance for Papillary Thyroid Microcarcinoma: New Challenges and Opportunities for the Health Care System[J]. Endocr Pract, 2016,22(5):602–611. doi: 10.4158/EP151065.RA.
[9]Ito Y, Miyauchi A, Oda H. Low-risk papillary microcarcinoma of the thyroid: A review of active surveillance trials[J]. Eur J Surg Oncol, 2017, pii: S0748–7983(17)30370–0. doi: 10.1016/j.ejso.2017.03.004. [Epub ahead of print]
[10]中國(guó)抗癌協(xié)會(huì)甲狀腺癌專業(yè)委員會(huì)(CATO). 甲狀腺微小乳頭狀癌診斷與治療中國(guó)專家共識(shí) (2016版)[J]. 中國(guó)腫瘤臨床, 2016,43(10):405–411. doi:10.3969/j.issn.1000–8179.2016.10.001.Chinese Association of Thyroid Oncology (CATO). Chinese experts consensus on diagnosis and treatment of papillary thyroid microcarcinoma (2016 edition)[J]. Chinese Journal of Clinical Oncology, 2016, 43(10):405–411. doi:10.3969/j.issn.1000–8179.2016.10.001.
[11]Iacobone M, Jansson S, Barczyński M, et al. Multifocal papillary thyroid carcinoma--a consensus report of the European Society of Endocrine Surgeons (ESES)[J]. Langenbecks Arch Surg, 2014,399(2):141–154. doi: 10.1007/s00423–013–1145–7.
[12]Kim HJ, Sohn SY, Jang HW, et al. Multifocality, but not bilaterality,is a predictor of disease recurrence/persistence of papillary thyroid carcinoma[J]. World J Surg, 2013, 37(2):376–384. doi: 10.1007/s00268–012–1835–2.
[13]So YK, Kim MW, Son YI. Multifocality and bilaterality of papillary thyroid microcarcinoma[J]. Clin Exp Otorhinolaryngol, 2015,8(2):174–178. doi: 10.3342/ceo.2015.8.2.174.
[14]Tam AA, ?zdemir D, ?uhac? N, et al. Association of multifocality,tumor number, and total tumor diameter with clinicopathological features in papillary thyroid cancer[J]. Endocrine, 2016, 53(3):774–783. doi: 10.1007/s12020–016–0955–0.
[15]單志東, 鞏鵬, 王忠裕. 多灶性甲狀腺乳頭狀癌的構(gòu)成比變化及臨床分析[J]. 國(guó)際外科學(xué)雜志, 2013, 40(5):306–310. doi:10.3760/cma.j.issn.1673–4203.2013.05.007.Shan ZD, Gong P, Wang ZY. Change of constituent ratio and clinical analysis of multifocal papillary thyroid carcinoma[J].International Journal of Surgery, 2013, 40(5):306–310. doi:10.3760/cma.j.issn.1673–4203.2013.05.007.
[16]嚴(yán)麗, 李情懷, 王樹(shù)峰, 等. 術(shù)前TSH水平與甲狀腺結(jié)節(jié)良惡性關(guān)系[J]. 中國(guó)普通外科雜志, 2012, 21(11):1373–1376.Yan L, Li QH, Wang SF, et al. Relationship between preoperative serum thyrotropin (TSH) level and the nature of thyroid nodule[J].Chinese Journal of General Surgery, 2012, 21(11):1373–1376.
[17]林琳, 鄭向前, 劉磊, 等. 多灶性甲狀腺乳頭狀癌的生物學(xué)特性及治療分析[J]. 中華普通外科雜志, 2010, 25(8):621–623. doi:10.3760/cma.j.issn.1007–631X.2010.08.006.Lin L, Zheng XQ, Liu L, et al. Multifocal papillary thyroid carcinoma[J]. Zhong Hua Pu Tong Wai Ke Za Zhi, 2010, 25(8):621–623. doi:10.3760/cma.j.issn.1007–631X.2010.08.006.
[18]Kim ES, Kim TY, Koh JM,et al. Completion thyroidectomy in patients with thyroid cancer who initially underwent unilateral operation[J]. Clin Endocrinol (Oxf), 2004, 61(1):145–148.
[19]殷德濤, 韓飏, 張亞原, 等. 多灶性甲狀腺乳頭狀癌的臨床病理及頸淋巴結(jié)轉(zhuǎn)移特征[J]. 中國(guó)普通外科雜志, 2017, 26(5):556–560.doi:10.3978/j.issn.1005–6947.2017.05.004.Yin DT, Han Y, Zhang YY, et al. Clinicopathologic and neck metastasis features of multifocal papillary thyroid cancer[J].Chinese Journal of General Surgery, 2017, 26(5):556–560.doi:10.3978/j.issn.1005–6947.2017.05.004.
[20]Koo BS, Lim HS, Lim YC, et al. Occult contralateral carcinoma in patients with unilateral papillary thyroid microcarcinoma[J]. Ann Surg Oncol, 2010, 17(4):1101–1105. doi: 10.1245/s10434–009–0906–6.
[21]Mercante G, Frasoldati A, Pedroni C, et al. Prognostic factors affecting neck lymph node recurrence and distant metastasis in papillary microcarcinoma of the thyroid: results of a study in 445 patients[J]. Thyroid, 2009, 19(7):707–716. doi: 10.1089/thy.2008.0270.
[22]孟慶東, 邊學(xué)海, 孫輝. 多灶性甲狀腺乳頭狀癌的診療進(jìn)展[J].中國(guó)普通外科雜志, 2016, 25(11):1640–1645. doi:10.3978/j.issn.1005–6947.2016.11.020.Meng QD, Bian XH, Sun H. Diagnosis and treatment of multifocal papillary thyroid carcinoma: recent progress[J]. Chinese Journal of General Surgery, 2016, 25(11):1640–1645. doi:10.3978/j.issn.1005–6947.2016.11.020.
[23]Liu LS, Liang J, Li JH, et al. The incidence and risk factors for central lymph node metastasis in cN0 papillary thyroid microcarcinoma: a meta-analysis[J]. Eur Arch Otorhinolaryngol,2017, 274(3):1327–1338. doi: 10.1007/s00405–016–4302–0.
[24]Zhao Q, Ming J, Liu C, et al. Multifocality and total tumor diameter predict central neck lymph node metastases in papillary thyroid microcarcinoma[J]. Ann Surg Oncol, 2013, 20(3):746–752. doi:10.1245/s10434–012–2654–2.
[25]Zhang L, Wei WJ, Ji QH, et al. Risk factors for neck nodal metastasis in papillary thyroid microcarcinoma: a study of 1066 patients[J]. J Clin Endocrinol Metab, 2012, 97(4):1250–1257. doi:10.1210/jc.2011–1546.
[26]Ganly I, Nixon IJ, Wang LY, et al. Survival from differentiated thyroid cancer: What has age got to do with it ?[J]. Thyroid, 2015,25(10):1106–1114. doi: 10.1089/thy.2015.0104.
[27]Nixon IJ, Kuk D, Wreesmann V, et al. De fi ning a valid age cutoffin staging of well-differentiated thyroid cancer[J]. Ann Surg Oncol,2016, 23(2):410–415. doi: 10.1245/s10434–015–4762–2.
[28]Lee KJ, Cho YJ, Kim SJ, et al. Analysis of the clinicopathologic features of papillary thyroid microcarcinoma based on 7-mm tumor size[J]. World J Surg, 2011, 35(2):318–323. doi: 10.1007/s00268–010–0886–5.
[29]Yoo HS, Shin MC, Ji YB, et al. Optimal extent of prophylactic central neck dissection for papillary thyroid carcinoma: Comparison of unilateral versus bilateral central neck dissection[J]. Asian J Surg, 2017, pii: S1015–9584(17)30011–8. doi: 10.1016/j.asjsur.2017.03.002. [Epub ahead of print]
[30]Seo GH, Chai YJ, Choi HJ, et al. Incidence of permanent hypocalcaemia after total thyroidectomy with or without central neck dissection for thyroid carcinoma: a nationwide claim study[J].Clin Endocrinol (Oxf), 2016, 85(3):483–487. doi: 10.1111/cen.13082.