牙韓清 鄭琴芳 何志鈞
摘要:潰瘍性結(jié)腸炎(UC)是一種慢性特發(fā)性腸道疾病,病程慢性遷延,可出現(xiàn)UC相關(guān)結(jié)直腸癌(UC-CRC)。近年來(lái),UC在亞洲地區(qū)的發(fā)病率呈上升趨勢(shì),隨著UC病程延長(zhǎng),UC-CRC的發(fā)病率也在增加,但UC-CRC的疾病特點(diǎn)與散發(fā)性CRC有所不同,疾病的治療更加復(fù)雜,延誤手術(shù)時(shí)機(jī)或不規(guī)范外科處理均會(huì)帶來(lái)不良的后果。為此,本文針對(duì)UC-CRC的個(gè)體化治療策略,就UC-CRC手術(shù)治療進(jìn)展進(jìn)行綜述,旨在為臨床治療UC-CRC提供參考。
關(guān)鍵詞:潰瘍性結(jié)腸炎;結(jié)直腸癌;癌變
Abstract:Ulcerative colitis (UC) is a chronic idiopathic intestinal disease with chronic disease progression and UC-related colorectal cancer (UC-CRC). In recent years, the incidence of UC in Asia has been on the rise. As the course of UC is prolonged, the incidence of UC-CRC is also increasing, but the disease characteristics of UC-CRC are different from sporadic CRC, and the treatment of the disease is more complicated,delayed operation timing or non-standard surgical treatment will bring undesirable consequences. To this end, this article reviews the progress of UC-CRC surgical treatment for the individualized treatment strategy of UC-CRC, and aims to provide a reference for clinical treatment of UC-CRC.
潰瘍性結(jié)腸炎(ulcerative colitis,UC)是一種好發(fā)于青壯年、持續(xù)或反復(fù)發(fā)作的慢性特發(fā)性腸道疾病,可出現(xiàn)中毒性巨結(jié)腸、腸穿孔、下消化道大出血以及癌變等嚴(yán)重并發(fā)癥。根據(jù)UC患者的嚴(yán)重程度、累及范圍和治療目標(biāo)個(gè)體化地選擇美沙拉嗪、糖皮質(zhì)激素、免疫抑制制、生物制劑等藥物,以及內(nèi)鏡和手術(shù)手術(shù)治療。近年來(lái),UC相關(guān)結(jié)直腸癌(UC-associated colorectal cancer,UC-CRC)的發(fā)病率呈上升趨勢(shì),其外科治療較散發(fā)性結(jié)直腸癌更加復(fù)雜。本文就UC-CRC的流行病學(xué)、危險(xiǎn)因素、內(nèi)鏡監(jiān)測(cè)及治療、外科手術(shù)的時(shí)機(jī)及方式等進(jìn)行綜述,為UC-CRC的外科治療提供一定的參考依據(jù)。
1流行病學(xué)及危險(xiǎn)因素
UC在歐美以北歐為最高發(fā)地區(qū),UC發(fā)病率和患病率分別達(dá)24.3/10萬(wàn)、505/10萬(wàn)[1,2]。亞洲地區(qū)中,韓國(guó)近30年來(lái)UC上升趨勢(shì),UC發(fā)病率為5.82/10萬(wàn),是1986年的20倍,男女比例1.2:1[3]。在中國(guó),UC發(fā)病率為(1.64~2.05)/10萬(wàn)[4,5],Zhai H等[6]研究發(fā)現(xiàn),2014年住院炎癥性腸病患者占全部胃腸道疾病住院患者的3.27%,比2002年增加2.07倍,其中85.19%為UC患者。Fumery M等[7]的隊(duì)列研究發(fā)現(xiàn),671例大腸中存在輕度不典型增生的UC患者,進(jìn)展為重度不典型增生的年合并發(fā)病率為1.8%,而進(jìn)展為CRC的年合并發(fā)病率達(dá)到0.8%;這其中約9.7%的低級(jí)別異型增生可能在1年內(nèi)進(jìn)展為高級(jí)別異形增生[8]。Kishikawa J等[9]對(duì)289例日本UC患者回顧性分析發(fā)現(xiàn)其20年的結(jié)直腸癌的累積風(fēng)險(xiǎn)為3.2%。張琴等[10]對(duì)3561例UC 患者的回顧性分析發(fā)現(xiàn)我國(guó)UC患者的總體癌變率為0.81%,低于西方國(guó)家報(bào)道的3.7%。
由于疾病的慢性遷延,UC診斷后5年的累積手術(shù)率約13.1%[11]。在接受外科手術(shù)的UC患者中,約12.5%~31.58%合并結(jié)直腸癌或者腸黏膜不典型增生[12-15]。Bopanna S等[16]研究發(fā)現(xiàn),亞洲人群UC-CRC累積發(fā)病率在10、20、30年分別為0.02%、4.8l%、13.91%;而Gong W等[17]研究顯示,我國(guó)UC患者UC-CRC累積發(fā)病率在10、20、30年分別1.15%、3.56%和14.36%,高于散發(fā)的結(jié)直腸癌患者[18],其發(fā)病率是正常人群的2~5倍[7]。
與UC-CRC相關(guān)的危險(xiǎn)因素主要有低齡起病、病程長(zhǎng)、腸道病變范圍廣泛、如原發(fā)性硬化性膽管炎等伴隨疾病、腸道黏膜持續(xù)炎癥、大腸癌家族史、強(qiáng)烈免疫抑制劑使用等[18-22]。細(xì)胞因子、一氧化氮、環(huán)氧酶、Toll樣受體4等各種促炎相關(guān)因子組成的腫瘤微環(huán)境,通過對(duì)腫瘤基因和抑癌基因的甲基化、調(diào)控基因異常表達(dá)等表觀遺傳學(xué)、NF-κB、絲裂酶原活化蛋白激酶等各種信號(hào)通路作用,以及遺傳因素、腸道菌群紊亂等刺激導(dǎo)致的慢性炎癥,經(jīng)“炎癥一異型增生一癌變”的途徑發(fā)展[23-26]。
2 UC-CRC的腸鏡特點(diǎn)和手術(shù)治療
UC-CRC腸鏡下癌灶可呈平坦、浸潤(rùn)或隆起型生長(zhǎng),表面多發(fā)的潰瘍面,背景黏膜可存在結(jié)節(jié)樣不平或黏膜無(wú)結(jié)構(gòu)區(qū),并可伴不同程度的腸腔狹窄[27]。放大內(nèi)鏡、色素內(nèi)鏡等技術(shù)可使UC-CRC診斷的敏感性和特異性達(dá)到72%以上,并可較好的進(jìn)行病變范圍的確定,提高病變陰性切除率[28]。規(guī)律內(nèi)鏡監(jiān)測(cè)的UC-CRC患者,其腫瘤分期偏向更早并可提高術(shù)后整體生存率[29]。一般腸鏡檢查應(yīng)在UC起病后6~10年開始,如合并原發(fā)性硬化性膽管炎,應(yīng)在確診后每年進(jìn)行結(jié)腸鏡檢查。
內(nèi)鏡下黏膜切除術(shù)和內(nèi)鏡下黏膜剝離術(shù)是常用的內(nèi)鏡下治療技術(shù)。Yuki S等[30]報(bào)道了一名50歲UC患者,直腸出現(xiàn)10 mm的平坦分化型管狀腺瘤且無(wú)浸潤(rùn)性生長(zhǎng),經(jīng)內(nèi)鏡下黏膜切除術(shù)達(dá)陰性切除的效果。Kinoshita S等[28]回顧性分析了25例緩解期UC合并結(jié)直腸不典型增生或腫瘤性病變患者,發(fā)現(xiàn)經(jīng)內(nèi)鏡下黏膜剝離術(shù)治療后其陰性切除率高達(dá)76%,術(shù)后出血及穿孔率極低,21周中位隨訪時(shí)間均未見原病灶處腫瘤復(fù)發(fā);說明內(nèi)鏡下黏膜剝離術(shù)既有切除病變?cè)\斷作用,又能在一定程度上達(dá)到治療目的。對(duì)于散發(fā)性腺瘤或隆起型腫塊上出現(xiàn)異型增生而不伴有周圍平坦黏膜上的異型增生時(shí),可行腸鏡下病變治療,因炎癥黏膜上出現(xiàn)息肉樣腺瘤患者,其癌變風(fēng)險(xiǎn)提高4倍,故內(nèi)鏡治療后仍需要密切內(nèi)鏡隨訪[31],并評(píng)估是否需要追加外科手術(shù),當(dāng)病變累及黏膜下層及以深或孤立病變周圍存在異型增生時(shí),宜行外科手術(shù)治療[32]。
需要說明的是,內(nèi)鏡下治療UC相關(guān)早期癌變、重度不典型增生病變的遠(yuǎn)期療效仍有待進(jìn)一步研究,尤其是多灶性不典型增生、黏膜下纖維化嚴(yán)重、處于UC活動(dòng)期等情況時(shí),需要審慎開展內(nèi)鏡下治療[33]。
3外科治療
UC病變的靶器官為結(jié)直腸,通過外科手術(shù)切除全部結(jié)直腸可達(dá)到治愈效果。UC-CRC的治療需要綜合結(jié)直腸癌治療原則,兼顧UC個(gè)體化手術(shù)治療需要[32,34],結(jié)合加速康復(fù)外科理念,可更好提高患者生存質(zhì)量[35]。癌變是UC外科手術(shù)的絕對(duì)適應(yīng)癥,在腫瘤治療的基礎(chǔ)上,UC的外科手術(shù)時(shí)機(jī)和方式需綜合考慮患者的年齡、全身情況、對(duì)排糞便的要求、病變腸段范圍和程度、腫瘤分期、肛管括約肌功能以及術(shù)者經(jīng)驗(yàn)等[14]。
3.1手術(shù)時(shí)機(jī)? UC急診外科手術(shù)率在近30年來(lái)由10.4%下降至0.5%[36]。多數(shù)患者病情較危重,伴貧血、營(yíng)養(yǎng)障礙、長(zhǎng)期應(yīng)用糖皮質(zhì)激素等情況,手術(shù)風(fēng)險(xiǎn)和術(shù)后并發(fā)癥發(fā)生率較高,應(yīng)注意加強(qiáng)多學(xué)科協(xié)助[14,37]。UC-CRC患者結(jié)直腸存在慢性炎癥的疾病特點(diǎn),雖然急診手術(shù)的并發(fā)癥發(fā)生率及病死率均較高,但拖延手術(shù)時(shí)機(jī)會(huì)增加術(shù)后并發(fā)癥[38]。最終約20%~30%的UC患者需要外科手術(shù),因合并消化道自發(fā)性穿孔、腸道大出血、中毒性巨結(jié)腸而需要手術(shù)的約占UC手術(shù)患者2.8%~13.8%、2.8%~16.1%、13.9%等,此類UC-CRC患者應(yīng)評(píng)估病情,行急診手術(shù)治療[39-42]。重癥UC患者在靜脈用足量激素治療的轉(zhuǎn)換時(shí)機(jī)從5 d更改為3 d(可結(jié)合病情,適當(dāng)延長(zhǎng)至7 d)[32]。Bernardo S等[43]總結(jié)112例重癥UC患者治療,發(fā)現(xiàn)42%的患者對(duì)靜脈激素?zé)o效,28.6%接受了轉(zhuǎn)換治療,最終26.8%接受了外科手術(shù)。
3.2手術(shù)方式? UC-CRC術(shù)前診斷明確時(shí),擇期根據(jù)腫瘤分期手術(shù)行結(jié)直腸癌手術(shù)治療切除癌變或疑癌腸段,并貼近血管根部離斷和清掃淋巴結(jié)基礎(chǔ)上,進(jìn)行一期或分期全結(jié)腸直腸切除+回腸儲(chǔ)袋肛管吻合術(shù),為目前最常用的手術(shù)方式[44]。對(duì)于無(wú)法根治性切除者,則評(píng)估姑息手術(shù)、輔助放化療[34]。在手術(shù)方式確立基礎(chǔ)上,根據(jù)情況,進(jìn)行傳統(tǒng)的開腹手術(shù)、腹腔鏡手術(shù)、手輔助腹腔鏡手術(shù)、經(jīng)自然腔道內(nèi)鏡手術(shù)、機(jī)器人輔助腹腔鏡手術(shù)等外科手術(shù)模式的選擇[45,46]。Wang YN等[47]回顧性分析25例UC-CRC的TNM分期,發(fā)現(xiàn)Ⅰ期、Ⅱ期、Ⅲ期、Ⅳ期患者占比分別為16.0%、40.0%、28.0%、16.0%,其中10例進(jìn)行了全結(jié)腸切除,13例進(jìn)行部分結(jié)腸切除,3例術(shù)后復(fù)發(fā),1例發(fā)生遠(yuǎn)處轉(zhuǎn)移。①腸襻修補(bǔ)/切除+造口術(shù):急診手術(shù)的目標(biāo)是以快捷切除病變結(jié)腸,緩解患者急診癥狀,搶救患者生命,并根據(jù)病情進(jìn)行分期手術(shù)治療[38]。對(duì)于患者全身情況差、腹腔內(nèi)感染嚴(yán)重時(shí),宜先行局部病變腸襻切除或穿孔修補(bǔ)+回腸末端造口術(shù);但對(duì)于單純腸穿孔修補(bǔ),可能出現(xiàn)穿孔部位愈合困難,甚至出現(xiàn)腸瘺及腹腔感染加重[48]。UC-CRC合并腸梗阻時(shí),多數(shù)患者營(yíng)養(yǎng)狀態(tài)欠佳,術(shù)前放置腸道支架,可降低術(shù)后并發(fā)癥發(fā)生率[49]。②結(jié)直腸癌手術(shù)+結(jié)直腸切除術(shù)+回腸末端造口術(shù)/回腸儲(chǔ)袋肛管吻合術(shù):若結(jié)腸病變廣泛且腫瘤未累及直腸,病情可耐受時(shí)行保留直腸的全結(jié)腸切除+回腸末端造口術(shù);2期或3期再綜合患者情況,并結(jié)合腫瘤分期,病情允許時(shí)行結(jié)合結(jié)直腸癌根治術(shù)所需要的對(duì)應(yīng)腸系膜血管的離斷和淋巴結(jié)清掃,并注意腹腔常規(guī)全面探查[34,50],行結(jié)腸次全切除+回腸末端造口術(shù)、全結(jié)腸直腸切除+回腸儲(chǔ)袋肛管吻合術(shù)。UC-CRC腫瘤位于直腸患者,根據(jù)腫瘤TNM分期,Tis、T1、T2(N0M0)可行直腸癌根治術(shù)治療,不需要輔助放化療[34],此時(shí)可進(jìn)行直腸癌根治術(shù),聯(lián)合全結(jié)腸直腸切除+回腸儲(chǔ)袋肛管吻合術(shù)。但當(dāng)直腸癌處于局部進(jìn)展期時(shí),因術(shù)后需要輔助放療[34],回腸儲(chǔ)袋對(duì)放療的耐受性差,增加吻合口瘺、儲(chǔ)袋炎等風(fēng)險(xiǎn),全結(jié)腸直腸切除+永久性的回腸造口可能是更合理的選擇,但I(xiàn)noue Y等[51]報(bào)道了1例UC合并進(jìn)展期直腸癌,術(shù)前先行放化療,隨后進(jìn)行全結(jié)腸直腸切除+回腸儲(chǔ)袋肛管吻合術(shù),恢復(fù)良好,術(shù)后1年未見復(fù)發(fā)??傊?,UC外科手術(shù)多種基本術(shù)式,目前以下兩種術(shù)式應(yīng)用較多:第一,全結(jié)腸直腸切除+回腸儲(chǔ)袋肛管吻合術(shù),為目前最常用的UC手術(shù)方式[52];第二,全結(jié)腸直腸切除+永久性回腸造口術(shù),該術(shù)式適用于肛門括約肌功能障礙或直腸遠(yuǎn)端有癌變的患者[53]。此外,對(duì)結(jié)直腸癌患者術(shù)前也應(yīng)排查潰瘍性結(jié)腸炎,因術(shù)前忽視了UC的病史而僅常規(guī)行結(jié)直腸癌手術(shù),術(shù)后并發(fā)癥的發(fā)生率將增高[54]。如Koyama M等[12]發(fā)現(xiàn)術(shù)前腸鏡檢查無(wú)癌的UC患者中,有5例(4.5%)術(shù)中合并結(jié)直腸癌,提示術(shù)中應(yīng)注意探查,尤其合并高危CRC因素的患者。
3.3手術(shù)局限性? 手術(shù)可以解決UC-CRC患者的一部分情況,但手術(shù)也帶來(lái)一定的相關(guān)并發(fā)癥:回腸儲(chǔ)袋肛管吻合術(shù)后患者儲(chǔ)袋炎患病率達(dá)28.5%~31.3%,可表現(xiàn)為排糞次數(shù)增多、排糞失禁、夜間滲液、里急后重、腹痛、盆腔疼痛和形成瘺管等[37,55],抗生素治療為治療急性儲(chǔ)袋炎的一線藥物,約4.2%~14%患者因嚴(yán)重儲(chǔ)袋炎或儲(chǔ)袋失功能無(wú)法耐受而切除回腸儲(chǔ)袋行永久造口[56,57]。而吻合口瘺、 腸梗阻、縫合口狹窄等發(fā)生率分別為30%、20%、16%,另外還存在脫水、結(jié)直腸癌等相關(guān)并發(fā)癥[14,37,57]。因UC嚴(yán)重的結(jié)腸炎癥病變有時(shí)難以區(qū)分UC與克羅恩病,病情觀察過程中約1.3%~28%UC術(shù)后患者修正診斷為克羅恩病,提醒注意術(shù)后評(píng)估,及時(shí)對(duì)疾病診斷重新修正[57]。
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收稿日期:2020-02-25;修回日期:2020-03-05
編輯/成森