临床小儿外科杂志  2024, Vol. 23 Issue (5): 401-404  DOI: 10.3760/cma.j.cn101785-202401058-001

引用本文  

刘远梅, 黄露, 金祝. 先天性巨结肠根治手术中直肠肌鞘切除的现状与思考[J]. 临床小儿外科杂志, 2024, 23(5): 401-404.   DOI: 10.3760/cma.j.cn101785-202401058-001
Liu YM, Huang L, Jin Z. Current status and reflections on rectal muscular cuff removal in Hirschsprung's disease[J]. J Clin Ped Sur, 2024, 23(5): 401-404.   DOI: 10.3760/cma.j.cn101785-202401058-001

基金项目

国家自然科学基金(82060100)

通信作者

刘远梅,Email: yuanmei116@aliyun.com

文章历史

收稿日期:2024-01-25
先天性巨结肠根治手术中直肠肌鞘切除的现状与思考
刘远梅 , 黄露 , 金祝     
贵州省儿童医院 遵义医科大学附属医院小儿外科,遵义 563000
摘要:先天性巨结肠(Hirschsprung's disease, HSCR)是小儿常见消化道疾病,手术切除病变肠段是其主要治疗方式。常用的手术方法包括Soave手术、Swenson手术、Duhamel手术、Rehbein手术等。如何预防及减少手术后并发症,是目前临床医师治疗HSCR的难点。而避免HSCR术后便秘、肌鞘感染、污粪、小肠结肠炎等并发症的关键因素是术中直肠肌鞘的精准处理。但是,目前尚无直肠肌鞘切除范围的统一标准。近年来,国内外研究人员通过改进各种手术方法以期减少术后并发症的发生。本文阐述国内外HSCR治疗的研究现状,并结合笔者多年临床体会,对术中直肠肌鞘切除的几个焦点问题进行总结和分析。
关键词先天性巨结肠    直肠肌鞘    外科手术    儿童    
Current status and reflections on rectal muscular cuff removal in Hirschsprung's disease
Liu Yuanmei , Huang Lu , Jin Zhu     
Department of Pediatric Surgery, Affiliated Hospital, Zunyi, Guizhou Children's Hospital, Zunyi 563000, China
Abstract: Hirschsprung's disease (HSCR) is a common gastrointestinal disorder in children.Surgical resection of affected intestinal segment represents a primary therapeutic approach for HSCR.Various surgical techniques of Soave, Swenson, Duhamel and Rehbein are commonly employed.And preventing and minimizing postoperative complications have constituted a great challenge and a focal point for clinicians treating HSCR.Precise intraoperative handling of rectal muscle cuff helps to avoid such postoperative complications as constipation, muscular cuff infection, fecal soiling and enterocolitis post-HSCR.Nonetheless, there is a lack of standardized guidelines regarding the extent of rectal muscle cuff resection Consequently, researchers worldwide have endeavored to refine surgical techniques for mitigating postoperative complications.This review focused upon a comprehensive analysis of key considerations during rectal muscle cuff resection, drawing upon current global researches and extensive personal clinical experiences.
Key words: Hirschsprung's Disease    Rectus Muscular Cuff    Surgical Procedures, Operative    Child    

先天性巨结肠(Hirschsprung's disease, HSCR)是小儿常见消化道畸形,发病率约1 ∶ 5 000,居消化道畸形发病率第二位,病因十分复杂,主要病理改变是结直肠肌间和黏膜下神经丛缺失神经节细胞,形成狭窄段病变组织[1]。根据无神经节细胞病变范围,HSCR分为短段型、长段型、全结肠型和全肠型[2]。自1948年Swenson首次采用手术治疗HSCR以来,逐渐演变出Swenson手术、Duhamel手术、Soave手术、Rehbein手术四种经典手术方法。目前,手术切除无神经节细胞肠管是HSCR的根治性方法,但术后污粪、小肠结肠炎(Hirschsprung associated enterocolitis, HAEC)、便秘复发、肌鞘感染、吻合口狭窄等并发症严重影响患儿生活质量。直肠肌鞘切除范围是影响HSCR根治手术后并发症的关键因素之一。如何预防及减少术后并发症,提高HSCR的治疗效果,更加精准处理直肠肌鞘,是目前临床医师治疗HSCR面临的难点,也是临床关注的焦点。近年来国内外小儿外科医师不断进行手术的改良和创新,但直肠肌鞘切除范围一直存在争议,目前尚无统一标准。本文针对HSCR手术中直肠肌鞘切除的焦点问题,结合当前国内外研究现状进行评述,为临床减少HSCR手术后并发症提供参考。

一、Soave手术以及改良Soave手术中直肠肌鞘切除的现状

Soave手术于1952年由Asa G Yancey首次提出[3]。由于Soave术操作简单、不需要解剖盆腔,是目前治疗HSCR最常用的手术方法。但是,该术式保留了5~7 cm的无神经节细胞直肠肌鞘,增加了肌鞘感染、便秘、HAEC等并发症发生率。针对并发症的发生原因,国内外学者对Soave手术进行了改良。2003年Rintala[4]提出不切开背侧肌层,保留1~3 cm短肌鞘经肛门拖出手术,经长期随访表明,该术式具有减少术后并发症的优势[5]。Nasr等[6]提出保留更短的肌鞘(< 2 cm),与保留长肌鞘的患儿相比,术后HAEC、吻合口狭窄的发生率均降低。Tang等[7]采用改良Soave手术,环形切开直肠肌鞘进入腹腔,保留2~3 cm肌鞘,术后括约肌痉挛、便秘复发和HAEC的发生率明显降低,而污便的发生率没有增加。2019年高明娟等[8]应用逐层梯度分离切除直肠肌鞘的方法,保留了部分内括约肌,术后污粪及HAEC的发生率均降低。以上研究表明,减少无神经节细胞直肠肌鞘残留,可明显减少术后并发症的发生。然而改良Soave手术仅仅把长肌鞘变成了短肌鞘,术后仍然残留部分无神经节细胞肠段,因此研究者们一直在不断探索精准处理直肠肌鞘的微创手术。随着科技的进步和手术设备的改进,近年来,达芬奇机器人系统(robotic surgery system)应运而生,机器人辅助Soave术治疗HSCR,通过更精准处理直肠肌鞘取得了较好的效果,术后约90%的患儿排便功能达到优良水平[9]。但其远期疗效还需要更多病例及更长时间的随访研究去证实,如何更有效精准处理直肠肌鞘,提高HSCR治疗效果,减少术后并发症,仍然是HSCR治疗面临的难点。

二、Swenson手术及改良Swenson手术中直肠肌鞘的处理现状

传统开腹Swenson手术操作范围广、创伤大,容易损伤盆腔神经及周围器官和组织。该手术保留了齿状线以上2 cm直肠肌鞘和内括约肌,污粪、吻合口瘘是其主要术后并发症。Zhuansun等[10]回顾性分析10年来应用“心形吻合术”治疗HSCR患儿的远期疗效,发现术后污粪、便失禁和便秘复发的发生率更低。该术式在国内多家医院被推广应用,并取得了较好的效果[11-14]。2013年Levitt等[15]报道了改良Swenson-like手术,保留了齿状线以上1 cm的直肠肌鞘,术后随访所有患儿自主排便功能良好,并发症明显减少。Zhang等[16]采用经肛门直肠黏膜切除和部分肛门内括约肌切除的改良Swenson手术,切除部分内括约肌和直肠肌鞘后壁,保留完整的外括约肌和直肠肌鞘前壁,在减少术后HAEC、便秘、污粪上更具优势。随着腹腔镜技术的不断发展,国内医师采用腹腔镜辅助Swenson-like术,在腹腔镜辅助下将直肠游离更低,直肠前壁仅保留1.5~2 cm,后壁保留1 cm,避免了Swenson手术的肌鞘残留和Duhamel手术的闸门所致并发症[17-18]。Yokota等[19-20]提出完整切除直肠肌鞘而无需广泛分离盆腔,可减少Swenson手术后功能性肠梗阻和排空障碍,减少了吻合口瘘及吻合口狭窄,且患儿获得较好的控便和排尿功能。由此可见,HSCR根治手术既要保证术后控便功能正常,又要避免术后便秘复发及HAEC,精准处理直肠肌鞘在预防及减少HSCR术后并发症中至关重要,但目前临床上尚无统一标准和专家共识指导。

三、Duhamel手术及改良Duhamel手术中直肠肌鞘的处理现状

传统Duhamel手术(结肠切除、直肠后结肠拖出术)是在腹腔游离结肠后横断直肠,通过直肠后隧道将近端结肠拖出与肛门后半壁切缘吻合,应用环钳夹闭直肠后壁与结肠前壁,该术式切除了约1/2的直肠后壁肌鞘,仍保留较长的无神经节细胞直肠前壁肌鞘,因此,便秘和粪便嵌塞成为Duhamel手术后的重要问题;如果钳夹吻合过低,容易引起盲袋和闸门症候群。Zhang等[21]报道的肛门外横断Duhamal手术以及Peters等[22]报道的改良Duhamal手术,均采用切割吻合器,消除盲袋和闸门,减少无神经节细胞直肠段的残留,且肛门外无环钳,减轻了患儿痛苦。该术式切除了约1/2的肛门内括约肌,容易引起术后污粪,根据长期随访结果,术后污粪会随着患儿年龄的增长而逐渐改善。由于改良Duhamel手术保留了前壁部分无神经节细胞肠管,建立了无神经节细胞-正常神经节细胞共同管道,增加了水分吸收,尤其适合治疗全结肠型巨结肠患者,可明显改善因术后污粪、小肠结肠炎、大便次数增多而引起的肛周红臀[23]

四、Rehbein手术及改良Rehbein手术中直肠肌鞘的处理现状

Rehbein手术(结肠切除、盆腔内低位直肠结肠吻合术)是在盆腔内完成直肠与正常结肠吻合。由于该术式不游离盆腔,没有切除直肠肌鞘和肛门内括约肌,因此创伤较小,但是该术式保留无神经节细胞肠管长度较长,术后便秘复发、小肠结肠炎等并发症的发生率较高。Meier等[24]报道了改良Rehbein手术,切除无神经节细胞肠管,保留距齿状线以上2~3 cm直肠肌鞘,采用21 mm圆形手术缝钉机吻合肠管。虽然术后并发症的发生率较低,但这可能与手术例数较少有关。王红等[25]报道了斜心形吻合和尽量缩短直肠下段保留长度,但仍有因吻合口狭窄、便秘复发而再次手术的情况,这可能与手术保留了相对较长的直肠肌鞘有关。2010年Visser等[26]报道了Rehbein手术治疗HSCR的临床经验,与Soave手术相比,Rehbein手术住院时间更长,术后发生肠梗阻、小肠结肠炎的概率明显增加,因此,Visser提出应该摒弃Rehbein手术。

五、展望

综上,临床医师对于HSCR手术后并发症的认识在不断提高,精准处理直肠肌鞘仍然是预防HSCR患儿手术后并发症、改善术后排便功能的关键。随着各类微创技术的不断创新,如何做到既微创、又保留肛门正常功能,探索更加科学、精准的HSCR外科治疗方案,依然任重道远。相信随着对HSCR研究的深入,新的治疗方法会逐渐出现,HSCR诊治水平将不断提升。近期Pan等[27]报道采用自体细胞移植治疗小鼠结直肠无神经节细胞病,相信对于预防和减少HSCR患儿手术后并发症、进而提高生活质量有一定的参考价值。

利益冲突  所有作者声明不存在利益冲突

参考文献
[1]
Montalva L, Cheng LS, Kapur R, et al. Hirschsprung disease[J]. Nat Rev Dis Primers, 2023, 9(1): 54. DOI:10.1038/s41572-023-00465-y
[2]
谢华, 唐维兵. 规范、统一先天性巨结肠分型的建议[J]. 临床小儿外科杂志, 2021, 20(3): 212-216.
Xie H, Tang WB. Unifying the classification types of Hirschsprung's disease[J]. J Clin Ped Sur, 2021, 20(3): 212-216. DOI:10.12260/lcxewkzz.2021.03.003
[3]
Woode D, Avansino J, Sawin R, et al. Asa G Yancey: the first to describe a modification of the Swenson technique for Hirschsprung disease[J]. J Pediatr Surg, 2022, 57(8): 1701-1703. DOI:10.1016/j.jpedsurg.2022.03.030
[4]
Rintala RJ. Transanal coloanal pull-through with a short muscular cuff for classic Hirschsprung's disease[J]. Eur J Pediatr Surg, 2003, 13(3): 181-186. DOI:10.1055/s-2003-41264
[5]
Rintala RJ. Long-term outcomes in newborn surgery[J]. Pediatr Surg Int, 2022, 39(1): 57. DOI:10.1007/s00383-022-05325-6
[6]
Nasr A, Langer JC. Evolution of the technique in the transanal pull-through for Hirschsprung's disease: effect on outcome[J]. J Pediatr Surg, 2007, 42(1): 36-40. DOI:10.1016/j.jpedsurg.2006.09.028
[7]
Tang ST, Wang GB, Cao GQ, et al. 10 years of experience with laparoscopic-assisted endorectal Soave pull-through procedure for Hirschsprung's disease in China[J]. J Laparoendosc Adv Surg Tech A, 2012, 22(3): 280-284. DOI:10.1089/lap.2011.0081
[8]
高明娟, 刘远梅, 祝代威. 腹腔镜辅助下经肛门逐层梯度切除直肠肌鞘改良Soave术治疗小婴儿先天性巨结肠的疗效分析[J]. 临床小儿外科杂志, 2019, 18(10): 839-843.
Gao MJ, Liu YM, Zhu DW. Laparoscopically assisted transanal gradient ablation of rectal muscle sheath for congenital megacolon in infants[J]. J Clin Ped Sur, 2019, 18(10): 839-843. DOI:10.3969/j.issn.1671-6353.2019.10.008
[9]
Mottadelli G, Erculiani M, Casella S, et al. Robotic surgery in Hirschsprung disease: a unicentric experience on 31 procedures[J]. J Robot Surg, 2023, 17(3): 897-904. DOI:10.1007/s11701-022-01488-5
[10]
Zhuansun DD, Jiao CL, Meng XY, et al. Long-term outcomes of laparoscope-assisted heart-shaped anastomosis for children with Hirschsprung disease: a 10-year review study[J]. J Pediatr Surg, 2020, 55(9): 1824-1828. DOI:10.1016/j.jpedsurg.2019.08.052
[11]
Li SX, Zhang HW, Cao H, et al. Clinical effects of ascending colon patching ileorectal heart-shaped anastomosis on total colonic aganglionosis[J]. Eur Rev Med Pharmacol Sci, 2017, 21(4 Suppl): 90-94.
[12]
黄磊, 易军, 王果. 先天性巨结肠患儿术后远期排便功能及行为心理状态研究[J]. 中华小儿外科杂志, 2012, 33(4): 284-287.
Huang L, Yi J, Wang g. Long-term follow-up of bowel function, behaviors and psychological situations of the children underwent operations for Hirschsprung's disease[J]. Chin J Pediatr Surg, 2012, 33(4): 284-287. DOI:10.3760/cma.j.issn.0253-3006.2012.04.011
[13]
许芝林, 肖友明, 赵铮, 等. 经肛门行改良Swenson巨结肠根治术疗效分析[J]. 中华小儿外科杂志, 2008, 29(10): 580-583.
Xu ZL, Xiao YM, Zhao Z, et al. Experience of modified Swenson operation for Hirschsprung's disease[J]. Chin J Pediatr Surg, 2008, 29(10): 580-583. DOI:10.3760/cma.j.issn.0253-3006.2008.10.002
[14]
汤绍涛, 王国斌, 阮庆兰. 腹腔镜辅助技术在先天性巨结肠手术中的应用价值[J]. 中华小儿外科杂志, 2007, 28(7): 347-350.
Tang ST, Wang GB, Ruan QL. The role of laparoscopic-assisted approaches in the treatment of Hirschsprung's disease[J]. Chin J Pediatr Surg, 2007, 28(7): 347-350. DOI:10.3760/cma.j.issn.0253-3006.2007.07.004
[15]
Levitt MA, Hamrick MC, Eradi B, et al. Transanal, full-thickness, Swenson-like approach for Hirschsprung disease[J]. J Pediatr Surg, 2013, 48(11): 2289-2295. DOI:10.1016/j.jpedsurg.2013.03.002
[16]
Zhang Z, Li Q, Li B, et al. Long-term Bowel function and pediatric health-related quality of life after transanal rectal mucosectomy and partial internal anal sphincterectomy pull-through for Hirschsprung Disease[J]. Front Pediatr, 2023, 11: 1099606. DOI:10.3389/fped.2023.1099606
[17]
潘伟康, 杨薇粒, 郑百俊, 等. 腹腔镜辅助Swenson-like巨结肠根治术105例[J]. 临床小儿外科杂志, 2018, 17(2): 112-116.
Pan WK, Yang WL, Zheng BJ, et al. Laparoscopic-assisted Swenson-like surgical approach for Hirschsprung's disease: a report of 105 cases[J]. J Clin Ped Sur, 2018, 17(2): 112-116. DOI:10.3969/j.issn.1671-6353.2018.02.007
[18]
曾纪晓, 徐晓钢, 刘斐, 等. 经脐单孔腹腔镜辅助下Swenson-like巨结肠根治术38例[J]. 临床小儿外科杂志, 2021, 20(9): 848-851, 865.
Zeng JX, Xu XG, Liu F, et al. Efficacies of transumbilical laparoendoscopic single-port surgery for Hirschsprung disease in children, a report of 38 cases[J]. J Clin Ped Sur, 2021, 20(9): 848-851, 865. DOI:10.12260/lcxewkzz.2021.09.009
[19]
Yokota K, Uchida H, Tainaka T, et al. Single-stage laparoscopic transanal pull-through modified Swenson procedure without leaving a muscular cuff for short-and long-type Hirschsprung disease: a comparative study[J]. Pediatr Surg Int, 2018, 34(10): 1105-1110. DOI:10.1007/s00383-018-4318-1
[20]
Yokota K, Amano H, Kudo T, et al. A novel Lugol's Iodine staining technique to visualize the upper margin of the surgical anal canal intraoperatively for Hirschsprung disease: a case series[J]. BMC Surg, 2020, 20(1): 317. DOI:10.1186/s12893-020-00986-3
[21]
Zhang X, Yang L, Tang ST, et al. Laparoscopic duhamel procedure with ex-anal rectal transection for right-sided Hirschsprung's disease[J]. J Laparoendosc Adv Surg Tech A, 2017, 27(9): 972-978. DOI:10.1089/lap.2016.0469
[22]
Peters NJ, Menon P, Rao KLN, et al. Modified Duhamel's two-staged procedure for Hirschsprung's disease: further modifications for improved outcomes[J]. J Indian Assoc Pediatr Surg, 2020, 25(5): 269-275. DOI:10.4103/jiaps.JIAPS_55_19
[23]
Wood RJ, Garrison AP. Total colonic aganglionosis in Hirschsprung disease[J]. Semin Pediatr Surg, 2022, 31(2): 151165. DOI:10.1016/j.sempedsurg.2022.151165
[24]
Meier H, Willital GH. Modified Rehbein surgical procedure using a surgical staple-progress in the treatment of Hirschsprung disease in children[J]. Langenbecks Arch Chir, 1987, 372: 751-753. DOI:10.1007/bf01297925
[25]
王红, 杨体泉, 唐咸明, 等. Rehbein术式改良法治疗先天性巨结肠243例[J]. 广西医科大学学报, 2004, 21(5): 713-714.
Wang H, Yang TQ, Tang XM, et al. Modified Rehbein procedure for congenital megacolon: a report of 243 cases[J]. J Guangxi Med Univ, 2004, 21(5): 713-714. DOI:10.3969/j.issn.1005-930X.2004.05.035
[26]
Visser R, van de Ven TJ, van Rooij IALM, et al. Is the Rehbein procedure obsolete in the treatment of Hirschsprung's disease?[J]. Pediatr Surg Int, 2010, 26(11): 1117-1120. DOI:10.1007/s00383-010-2696-0
[27]
Pan WK, Rahman AA, Ohkura T, et al. Autologous cell transplantation for treatment of colorectal aganglionosis in mice[J]. Nat Commun, 2024, 15(1): 2479. DOI:10.1038/s41467-024-46793-9