陸秀萍 姜海行 覃山羽 雷榮娥 謝明智 李曉敏
(廣西醫(yī)科大學(xué)第一附屬醫(yī)院消化內(nèi)科,南寧市 530021)
膽管細(xì)胞癌約占消化道腫瘤的3%,在世界范圍內(nèi)其發(fā)病率和死亡率都呈現(xiàn)上升的趨勢(shì)。當(dāng)患者被診斷膽管癌時(shí)往往已經(jīng)處于疾病進(jìn)展期,其預(yù)后較差[1]。根據(jù)Silva等[2,3]研究報(bào)道,手術(shù)后切緣陰性的膽管癌患者,1年、3年、5年的生存率分別為85%~100%、45%~80%、30%~45%。因此,為提高膽管癌患者生存率,需要較好的診斷工具以促進(jìn)對(duì)膽管癌的早期診斷。傳統(tǒng)的US、CT、MRI、MRCP對(duì)膽管擴(kuò)張?jiān)\斷的敏感性很高,然而這些成像模式不能確定膽管擴(kuò)張的病因、病灶的位置或病灶的范圍,介入方法如內(nèi)鏡下逆行胰膽管造影術(shù)(endoscopic retrograde cholangiopancreatography,ERCP)、膽道刷檢及活檢可用于下一步的協(xié)助診斷。但即使如此,仍有1/3的患者是診斷不明確的[4]。膽管內(nèi)超聲(intraductal ultrasonography,IDUS)是通過(guò)ERCP途徑將微型超聲探頭插入膽管內(nèi)進(jìn)行檢查。1992年Yasuda等[5,6]將IDUS應(yīng)用于膽胰疾病的診斷。膽管狹窄于IDUS圖像上具有特征性表現(xiàn)。有研究表明,IDUS的應(yīng)用使ERCP對(duì)良惡性膽管狹窄診斷的準(zhǔn)確性從58%上升至90%[7,8]。本文就IDUS在膽管狹窄性疾病的超聲圖像特征、IDUS對(duì)膽管癌的診斷、IDUS引導(dǎo)下聯(lián)合靶向膽管刷檢等研究進(jìn)展做一綜述。
1.1 正常膽管IDUS聲像圖 正常膽總管壁厚度為1~2 mm,20 MHz IDUS顯示膽總管壁為三層結(jié)構(gòu),膽管壁由內(nèi)向外其聲像圖呈強(qiáng)回聲-低回聲-強(qiáng)回聲,內(nèi)層強(qiáng)回聲為膽總管黏膜層及界面波;中層低回聲為纖維肌層及外筋膜;外層強(qiáng)回聲為漿膜下組織層。但是,臨床上顯示膽總管壁多為兩層結(jié)構(gòu)[9,10]。
1.2 惡性膽管病變IDUS聲像圖 可表現(xiàn)為膽管壁偏心性增厚、管壁結(jié)構(gòu)破壞、層次不清或消失;其特征是沿膽管壁向腔內(nèi)突出的低回聲軟組織影、膽管外層高回聲雜亂斷裂聲像、出現(xiàn)周?chē)馨徒Y(jié)腫大及血管浸潤(rùn)[9,10]。
IDUS是在導(dǎo)絲引導(dǎo)下將微型高頻率超聲探頭插入膽管內(nèi),這使大多數(shù)患者避免十二指腸乳頭切開(kāi);IDUS可以以超聲探頭為中心360°徑向?qū)崟r(shí)顯示膽管及其周?chē)M織的超聲圖像,其可見(jiàn)深度約為20 mm,分辨率達(dá)到0.1 mm[11]。而IDUS在提供詳細(xì)的高分辨率的膽道超聲圖像同時(shí),并沒(méi)有明顯延長(zhǎng)ERCP操作時(shí)間。此外,盡管遠(yuǎn)處轉(zhuǎn)移和淋巴結(jié)轉(zhuǎn)移可能超出超聲設(shè)備的成像領(lǐng)域,IDUS仍可以對(duì)惡性腫瘤進(jìn)行局部區(qū)域分期,以利于患者盡早接受手術(shù)治療,提高患者預(yù)后[12]。而根據(jù)上述IDUS對(duì)膽管狹窄患者診斷的準(zhǔn)確性達(dá)83%~90%。Tamada等[13]的一項(xiàng)多重回歸分析表明,對(duì)于膽管內(nèi)外表現(xiàn)為無(wú)柄狀腫瘤、腫瘤直徑>10.0 mm及膽管壁不規(guī)則增厚、中斷都是預(yù)測(cè)惡性膽管狹窄的獨(dú)立變量。根據(jù)這些診斷依據(jù),Meister等[11]研究指出,IDUS對(duì)膽管癌的診斷更具優(yōu)越性,診斷的敏感性達(dá)97.6%。然而也應(yīng)該特別注意良性膽管狹窄在IDUS上也可表現(xiàn)為不對(duì)稱性膽管壁增厚,如原發(fā)性硬化性膽管炎。有研究表明放置膽道支架大于14 d則可導(dǎo)致膽管壁的增厚,這可能是炎癥反應(yīng)的結(jié)果[14]。因此,對(duì)影響膽管壁增厚的因素要有更好的理解,才更利于對(duì)膽管狹窄性疾病的鑒別診斷。
當(dāng)腹部超聲或CT提示膽道系統(tǒng)擴(kuò)張時(shí),MRCP和(或)ERCP將被應(yīng)用于下一步的診療措施中。根據(jù)Ang等[15]對(duì)MRCP與ERCP的比較,其對(duì)良惡性膽管狹窄鑒別診斷的準(zhǔn)確性分別為58%和76%;而另一項(xiàng)前瞻性的研究表明,腹部超聲顯示不明原因膽總管擴(kuò)張>8 mm且處于非黃疸階段的肝外膽管癌,MRCP對(duì)其診斷的敏感性達(dá)90%[16]。然而MRCP無(wú)法得到膽管癌的組織病理學(xué)診斷,這將會(huì)延誤患者的診治;對(duì)于膽管癌患者如不予積極治療措施,95%患者將于1~2年內(nèi)死亡。ERCP可以介入膽道系統(tǒng)進(jìn)行膽管造影和膽道刷檢,Park等[17]研究表明ERCP診斷膽管癌的敏感性和特異性分別為74%和70%。由此可見(jiàn)對(duì)于MRCP、ERCP對(duì)膽管癌診斷的準(zhǔn)確性仍不是很高,應(yīng)該尋求更好的診斷方法以提高對(duì)膽管癌診斷的準(zhǔn)確性。IDUS聯(lián)合ERCP已被報(bào)道可以提高膽管癌的診斷準(zhǔn)確性。對(duì)于良惡性膽管狹窄的鑒別,ERCP+IDUS比MRCP能夠提供更可靠和精確的信息。Inui等[7,18]研究表明,IDUS對(duì)鑒別診斷膽管狹窄性疾病的準(zhǔn)確性為89.1%、敏感性為91.1%、特異性為84%;而另一項(xiàng)研究報(bào)道IDUS對(duì)膽管癌診斷的準(zhǔn)確性達(dá)到83%~90%[7]。IDUS對(duì)于原發(fā)性硬化性膽管炎背景下膽管癌患者的診斷也具有一定優(yōu)勢(shì),Tischendorf等[19]研究中根據(jù)IDUS上表現(xiàn)為膽管壁結(jié)構(gòu)中斷、膽管壁不對(duì)稱增厚及團(tuán)快性占位致膽管腔狹窄作為診斷惡性依據(jù),其對(duì)膽管癌診斷的敏感性和特異性為87.5%和90.6%,該研究的40例患者中只有1例假陰性和3例假陽(yáng)性結(jié)果。
膽管癌的分期是根據(jù)原發(fā)病灶大小、淋巴結(jié)轉(zhuǎn)移及遠(yuǎn)處轉(zhuǎn)移情況進(jìn)行判斷。根據(jù)IDUS超聲圖像上腫瘤大小回聲和膽管壁層次結(jié)構(gòu)情況可對(duì)膽管癌進(jìn)行T分期。然而實(shí)際上并不能區(qū)分T1和T2期腫瘤,因?yàn)镮DUS圖像上不能完全區(qū)分纖維肌層和漿膜下組織層,且內(nèi)部低回聲層對(duì)應(yīng)的不僅是纖維肌層,也包括一部分肌層周?chē)慕Y(jié)締組織。因此即使病灶局限于內(nèi)部的低回聲層,提示為T(mén)2期(腫瘤侵犯肌層周?chē)Y(jié)締組織),但也可以是T1期(腫瘤存在黏膜層),所以通過(guò)IDUS辨別T1和T2期腫瘤是困難的[20]。根據(jù)Menzel等[21]研究報(bào)道,IDUS對(duì)腫瘤T分期的準(zhǔn)確性為77.7%;而另一項(xiàng)對(duì)174例膽管惡性腫瘤患者的研究中表明IDUS對(duì)膽管癌的T1、T2和T3分期診斷的準(zhǔn)確性分別為84%、73%和71%[11]。對(duì)于膽管癌的N分期,IDUS次于EUS;EUS與IDUS比較對(duì)膽管癌N分期診斷準(zhǔn)確性分別為60%~64.9%和40%~62.5%[21,22];因?yàn)镮DUS的高分辨率限制其聲波穿透的深度,從而影響他對(duì)遠(yuǎn)處病灶的評(píng)估。而根據(jù)Tamada等[23]的描述,超聲圖像上表現(xiàn)為低回聲邊界清楚病灶、直徑>5.3 mm的圓形淋巴結(jié)被認(rèn)為是惡性腫大淋巴結(jié),而一個(gè)形狀不規(guī)則直徑較小的淋巴結(jié)被認(rèn)為是炎性腫大淋巴結(jié),用這一診斷標(biāo)準(zhǔn)的IDUS評(píng)估淋巴結(jié)轉(zhuǎn)移的準(zhǔn)確性提升至75%~78%。
IDUS對(duì)膽管癌縱向擴(kuò)張范圍的評(píng)估也有較高的準(zhǔn)確性。根據(jù)Tamada等[24]研究報(bào)道,與ERCP相比,IDUS對(duì)膽管癌向肝臟縱向擴(kuò)張?jiān)\斷的準(zhǔn)確性為84%與47%(P<0.05),膽管癌向十二指腸縱向擴(kuò)張?jiān)\斷的準(zhǔn)確性為86%與43%(P<0.05);而ERCP和IDUS對(duì)膽管癌總體縱向擴(kuò)張范圍診斷的準(zhǔn)確性分別為60%和90%[25]。
為提升膽管癌診斷的準(zhǔn)確性及評(píng)估其侵犯周?chē)M織結(jié)構(gòu)的情況,近年來(lái)3D-IDUS也被應(yīng)用于對(duì)膽管癌的診斷。3D-IDUS能對(duì)所獲取的圖像數(shù)據(jù)進(jìn)行重建,使病灶多平面顯示,從而更有利于判斷腫瘤的形態(tài)、腫瘤沿管壁生長(zhǎng)情況及其侵犯周?chē)M織結(jié)構(gòu)的情況[26]。有研究報(bào)道,3D-IDUS對(duì)評(píng)估腫瘤侵犯門(mén)靜脈的準(zhǔn)確性為100%[7,27],而IDUS為92%~100%;3D-IDUS對(duì)診斷腫瘤侵犯胰腺的準(zhǔn)確性為90%,而IDUS為80%。而Inui等[28]研究表明3D-IDUS的缺陷在于對(duì)腫瘤縱向擴(kuò)展范圍的評(píng)估。
雖然IDUS對(duì)膽管癌的診斷有較高的準(zhǔn)確性和敏感性,但其不能取得組織細(xì)胞學(xué)診斷。獲取膽管組織細(xì)胞標(biāo)本的途徑包括ERCP過(guò)程中的膽道刷檢、活檢或是兩者的聯(lián)合應(yīng)用。研究表明ERCP時(shí)進(jìn)行膽道刷檢對(duì)膽管癌診斷的特異性可達(dá)100%[17,29],而敏感性較低,僅23%~80%;其診斷低敏感性在于膽管刷檢所獲取細(xì)胞數(shù)量較少及獲取細(xì)胞存在細(xì)胞分裂有關(guān)。且對(duì)比狹窄膽管進(jìn)行擴(kuò)張?zhí)幚砬昂竽懝芩z,對(duì)膽管癌診斷的敏感性差異沒(méi)有統(tǒng)計(jì)學(xué)差異,而擴(kuò)張前和擴(kuò)張后刷檢結(jié)果的聯(lián)合分析可使膽管癌診斷的準(zhǔn)確性從35%升至44%(P=0.001)[30];改進(jìn)刷子的長(zhǎng)度和硬度亦不能改善診斷的結(jié)果[29]。而Weber等[31]報(bào)道膽管下段癌患者經(jīng)乳頭活檢的敏感性為84%~89%;對(duì)于肝門(mén)部膽管癌單純刷檢的敏感性為41.4%,活檢的敏感性為53.4%,刷檢聯(lián)合活檢的敏感性為60.3%。由此可見(jiàn),對(duì)于膽管癌的診斷,通過(guò)單純的膽道刷檢和(或)活檢得到病因診斷的準(zhǔn)確性還是較低的。而IDUS不僅可以在超聲圖像上提供良惡性依據(jù),而且在X線引導(dǎo)下可以協(xié)助對(duì)病灶定位,以促進(jìn)靶向細(xì)胞的刷檢,從而提高診斷的陽(yáng)性率。另有研究表明[32,33],IDUS聯(lián)合膽道刷檢對(duì)膽管癌診斷的準(zhǔn)確性為80.85%、敏感性為86.87%。而Farrell等[34]研究表明,對(duì)于懷疑惡性膽管癌而細(xì)胞刷檢陰性時(shí)加用IDUS對(duì)診斷的準(zhǔn)確性為92%、敏感性和特異性分別為90%和93%。
為提高細(xì)胞學(xué)診斷的陽(yáng)性率,數(shù)字化圖像分析(DIA)和熒光原位雜交技術(shù)(FISH)已被用于提高膽管細(xì)胞學(xué)診斷的敏感性。對(duì)于細(xì)胞數(shù)量有限的標(biāo)本DIA和FISH都是有用的。DIA是觀察單個(gè)細(xì)胞內(nèi)DNA成分情況,F(xiàn)ISH則是分析DNA內(nèi)多條染色體的情況[26]。一項(xiàng)前瞻性的研究中表明,當(dāng)常規(guī)的細(xì)胞學(xué)刷檢陰性時(shí),與常規(guī)細(xì)胞學(xué)相比,F(xiàn)ISH可以增加診斷的敏感性(30%~60%),特異性為98%;而常規(guī)細(xì)胞學(xué)特異性為100%[35];DIA的敏感性和特異性沒(méi)有特殊變化。對(duì)于膽管刷檢和活檢均為陰性的患者,DIA、FISH和DIA聯(lián)合FISH預(yù)測(cè)診斷惡性病變的準(zhǔn)確性分別為14%、62%和67%[36]。這些研究表明FISH是一項(xiàng)重要的改進(jìn)細(xì)胞學(xué)診斷能力的技術(shù)。
此外,超聲內(nèi)鏡引導(dǎo)下細(xì)針穿刺活檢術(shù)(EUS-FNA)也是一項(xiàng)提高細(xì)胞學(xué)診斷率的方法。有2項(xiàng)前瞻性的研究評(píng)價(jià)了EUS-FNA在膽管狹窄性疾病中的診斷價(jià)值。在第1項(xiàng)研究中41例肝門(mén)部狹窄患者均進(jìn)行 EUS-FNA,其對(duì)膽管癌診斷的準(zhǔn)確性、敏感性和特異性分別為91%、89%和100%[37]。在第2項(xiàng)研究中,28例無(wú)法通過(guò)常規(guī)刷檢或活檢進(jìn)行診斷的患者亦全部進(jìn)行EUS-FNA,其診斷膽管癌的準(zhǔn)確性、敏感性和特異性分別為88%、86%和100%[38];且EUS-FNA具有識(shí)別區(qū)域或遠(yuǎn)處淋巴結(jié)能力。由此可見(jiàn)EUS-FNA對(duì)于膽管癌患者的診斷也具有積極作用,使其他方法仍不能明確診斷的膽管癌患者可得到及時(shí)診斷,而不延誤患者接受手術(shù)治療的機(jī)會(huì),也避免了對(duì)良性膽管狹窄患者進(jìn)行錯(cuò)誤手術(shù)。
IDUS對(duì)膽管癌的診斷起著重要作用,依據(jù)膽管癌于IDUS上有特征性的聲像圖像表現(xiàn)可以提高對(duì)腫瘤的檢測(cè)率,尤其在原發(fā)性硬化性膽管炎背景下對(duì)膽管癌的檢出率也較高。IDUS對(duì)于膽管癌的T分期和縱向擴(kuò)張范圍診斷的準(zhǔn)確性較高,但由于其穿透深度的限制,對(duì)淋巴結(jié)轉(zhuǎn)移的分期不足。而3D-IDUS的應(yīng)用可以促進(jìn)對(duì)膽管癌浸潤(rùn)范圍的判斷。ERCP過(guò)程中聯(lián)合IDUS和膽管刷檢可以提高膽管癌診斷的陽(yáng)性率,而對(duì)細(xì)胞學(xué)檢測(cè)新方法,F(xiàn)ISH技術(shù)的應(yīng)用可以增加對(duì)數(shù)量有限的腫瘤標(biāo)本的檢出率。對(duì)細(xì)胞刷檢陰性尤其肝門(mén)部膽管癌時(shí),可以用EUS-FNA方法,其可以提高診斷的準(zhǔn)確性。
[1] Blechacz B,Komuta M,Roskams T,et al.Clinical diagnosis and staging of cholangiocarcinoma[J].Nature Reviews Gastroenterology & Hepatology,2011,8(9):512-522.
[2] Silva MA,Tekin K,Aytekin F,et al.Surgery for hilar cholangiocarcinoma;a 10 year experience of a tertiary referral centre in the UK[J].European Journal of Surgical Oncology,2005,31(5):533-539.
[3] Jarnagin WR,Bowne W,Klimstra DS,et al.Papillary phenotype confers improved survival after resection of hilar cholangiocarcinoma[J]. Annals of Surgery,2005,241(5):703-712;discussion 712-704.
[4] Glasbrenner B,Ardan M,Boeck W,et al.Prospective evaluation of brush cytology of biliary strictures during endoscopic retrograde cholangiopancreatography[J].Endoscopy,1999,31(9):712-717.
[5] Yasuda K,Mukai H,Nakajima M,et al.Clinical application of ultrasonic probes in the biliary and pancreatic duct[J].Endoscopy,1992,24(Suppl 1):370-375.
[6] Furukawa T,Naitoh Y,Tsukamoto Y,et al.New technique using intraductal ultrasonography for the diagnosis of diseases of the pancreatobiliary system[J].Journal of Ultrasound in Medicine,1992,11(11):607-612.
[7] Stavropoulos S,Larghi A,Verna E,et al.Intraductal ultrasound for the evaluation of patients with biliary strictures and no abdominal mass on computed tomography[J].Endoscopy,2005,37(8):715-721.
[8] Krishna NB,Saripalli S,Safdar R,et al.Intraductal US in evaluation of biliary strictures without a mass lesion on CT scan or magnetic resonance imaging:significance of focal wall thickening and extrinsic compression at the stricture site[J].Gastrointest Endosc,2007,66(1):90-96.
[9] 中華醫(yī)學(xué)會(huì)消化內(nèi)鏡分會(huì)ERCP學(xué)組,ERCP診治指南(2010版)(二)[J].中華消化內(nèi)鏡雜志,2010,27(4):169-172.
[10] Nguyen K,Sing JT,Jr.Review of endoscopic techniques in the diagnosis and management of cholangiocarcinoma[J].World Journal of Gastroenterology,2008,14(19):2995-2999.
[11] Meister T,Heinzow HS,Woestmeyer C,et al.Intraductal ultrasound substantiates diagnostics of bile duct strictures of uncertain etiology[J].World Journal of Gastroenterology,2013,19(6):874-881.
[12] Victor DW,Sherman S,Karakan T,et al.Current endoscopic approach to indeterminate biliary strictures[J].World journal of gastroenterology,2012,18(43):6197-6205.
[13] Tamada K,Tomiyama T,Wada S,et al.Endoscopic transpapillary bile duct biopsy with the combination of intraductal ultrasonography in the diagnosis of biliary strictures[J].Gut,2002,50(3):326-331.
[14] Varadarajulu S,Eloubeidi MA.The role of endoscopic ultrasonography in the evaluation of pancreatico-biliary cancer[J].The Surgical Clinics of North America,2010,90(2):251-263.
[15] Ang TL,Fock KM.Intraductal ultrasound in biliary disorders[J].Journal of Gastroenterology and Hepatology,2008,23(10):1468-1470.
[16] Sai JK,Suyama M,Kubokawa Y,et al.Early detection of extrahepatic bile-duct carcinomas in the nonicteric stage by using MRCP followed by EUS[J].Gastrointest Endosc,2009,70(1):29-36.
[17] Park MS,Kim TK,Kim KW,et al.Differentiation of extrahepatic bile duct cholangiocarcinoma from benign stricture:findings at MRCP versus ERCP[J].Radiology,2004,233(1):234-240.
[18] Inui K,Yoshino J,Miyoshi H.Differential diagnosis and treatment of biliary strictures[J].Clin Gastroenterol Hepatol,2009,7(11):S79-S83.
[19] Tischendorf JJW,Meier PN,Schneider A,et al.Transpapillary intraductal ultrasound in the evaluation of dominant bile duct stenoses in patients with primary sclerosing cholangitis[J].Scandinavian Journal of Gastroenterology,2007,42(8):1011-1017.
[20] Tamada K,Kanai N,Ueno N,et al.Limitations of intraductal ultrasonography in differentiating between bile duct cancer in stage T1 and stage T2:in-vitro and in-vivo studies[J].Endoscopy,1997,29(8):721-725.
[21] Menzel J,Poremba C,Dietl KH,et al.Preoperative diagnosis of bile duct strictures-comparison of intraductal ultrasonography with conventional endosonography[J].Scandinavian Journal of Gastroenterology,2000,35(1):77-82.
[22] Fujita N,Noda Y,Kobayashi G,et al.Intraductal ultrasonography (IDUS) for the diagnosis of biliopancreatic diseases[J].Best Pract Res Clin Gastroenterol,2009,23(5):729-742.
[23] Tamada K,Ushio J,Sugano K.Endoscopic diagnosis of extrahepatic bile duct carcinoma: Advances and current limitations[J].World Journal of Clinical Oncology,2011,2(5):203-216.
[24] Tamada K,Nagai H,Yasuda Y,et al.Transpapillary intraductal US prior to biliary drainage in the assessment of longitudinal spread of extrahepatic bile duct carcinoma[J].Gastrointest Endosc,2001,53(3):300-307.
[25] Choi ER,Chung YH,Lee JK,et al.Preoperative evaluation of the longitudinal extent of borderline resectable hilar cholangiocarcinoma by intraductal ultrasonography[J].Journal of Gastroenterology and Hepatology,2011,26(12):1804-1810.
[26] Levy MJ,Baron TH,Clayton AC,et al.Prospective evaluation of advanced molecular markers and imaging techniques in patients with indeterminate bile duct strictures[J].The American Journal of Gastroenterology,2008,103(5):1263-1273.
[27] Inui K,Miyoshi H.Cholangiocarcinoma and intraductal sonography[J].Gastrointestinal Endoscopy Clinics of North America,2005,15(1):143-155,x.
[28] Inui K,Yoshino J,Okushima K,et al.Intraductal EUS[J].Gastrointest Endosc,2002,56(4 Suppl):S58-62.
[29] Fogel EL,deBellis M,McHenry L,et al.Effectiveness of a new long cytology brush in the evaluation of malignant biliary obstruction:a prospective study[J].Gastrointest Endosc,2006,63(1):71-77.
[30] de Bellis M,Fogel EL,Sherman S,et al.Influence of stricture dilation and repeat brushing on the cancer detection rate of brush cytology in the evaluation of malignant biliary obstruction[J].Gastrointest Endosc,2003,58(2):176-182.
[31] Weber A,von Weyhern C,Fend F,et al.Endoscopic transpapillary brush cytology and forceps biopsy in patients with hilar cholangiocarcinoma[J].World Journal of Gastroenterology,2008,14(7):1097-1101.
[32] Soyuer I,Tasdemir A,Gursoy S,et al.Endoscopic biliary tract brush cytology in 54 cases[J].Turk J Med Sci,2010,40(5):807-812.
[33] Liu F,Li F,Zhou Y,et al.Intraductal ultrasound improves diagnostic yield for ERCP and cytology brushing in detecting malignant bile duct strictures for patients without biliary mass lesions on CT or MRI[C].Gastrointest Endosc,2008,67(5):AB228.
[34] Farrell RJ,Agarwal B,Brandwein SL,et al.Intraductal US is a useful adjunct to ERCP for distinguishing malignant from benign biliary strictures[J].Gastrointest Endosc,2002,56(5):681-687.
[35] Gonda TA,Glick MP,Sethi A,et al.Polysomy and p16 deletion by fluorescence in situ hybridization in the diagnosis of indeterminate biliary strictures[J].Gastrointest Endosc,2012,75(1):74-79.
[36] Fritcher EGB,Kipp BR,Halling KC,et al.A multivariable model using advanced cytologic methods for the evaluation of indeterminate pancreatobiliary strictures[J].Gastroenterology,2009,136(7):2180-2186.
[37] Fritscher-Ravens A,Broering DC,Knoefel WT,et al.EUS-guided fine-needle aspiration of suspected hilar cholangiocarcinoma in potentially operable patients with negative brush cytology[J].The American Journal of Gastroenterology,2004,99(1):45-51.
[38] Eloubeidi MA,Chen VK,Jhala NC,et al.Endoscopic ultrasound-guided fine needle aspiration biopsy of suspected cholangiocarcinoma[J].Clinical Gastroenterology and Hepatology,2004,2(3):209-213.