• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

所有短段型先天性巨结肠病患者都一样吗?一项回顾性多中心研究。

Are all patients with short segment Hirschsprung's disease equal? A retrospective multicenter study.

作者信息

Chung Patrick Ho Yu, Wong Kenneth Kak Yuen, Tam Paul Kwong Hang, Leung Michael Wai Yip, Chao Nicholas Sih Yin, Liu Kelvin Kam Wing, Chan Edwin Kin Wai, Tam Yuk Him, Lee Kim Hung

机构信息

Division of Pediatric Surgery, Department of Surgery, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 102, Pokfulam Road, Hong Kong, China.

Division of Pediatric Surgery, Department of Surgery, Queen Elizabeth Hospital, Hong Kong, China.

出版信息

Pediatr Surg Int. 2018 Jan;34(1):47-53. doi: 10.1007/s00383-017-4202-4. Epub 2017 Oct 26.

DOI:10.1007/s00383-017-4202-4
PMID:29075908
Abstract

BACKGROUND/PURPOSE: Short segment Hirschsprung's disease (HSCR) carries a better prognosis than long segment disease, but the definition of short is controversial. The objective of this study is to determine anatomically the extent of disease involvement that would be associated with a better functional outcome.

METHODS

This is a retrospective multicenter (n = 3) study with patients (≥ 3 years) who had transanal pullthrough operation done for aganglionosis limited to the recto-sigmoid colon were reviewed. The extent of disease involvement and bowel resection was retrieved by reviewing the operative records as well as histopathological reports of the resected specimens. Clinical assessment was performed according to the criteria of a seven-itemed bowel function score (BFS) (maximum score = 20). Manometric assessment was performed with anorectal manometry.

RESULTS

The study period started from 2003 to 45 patients were studied with median age at assessment = 52.0 months and operation = 3.0 months. The disease involvement was categorized into upper sigmoid-descending colon (DC) (n = 8), sigmoid colon (SC) (n = 12), upper rectum (UR) (n = 14) and lower rectum (LR) (n = 11) according to the level of normal biopsy result. There was no significant difference in the age of assessment between the four groups. The median BFSs in the DC, SC, UR and LR were 13, 15, 17 and 17, respectively (p = 0.01). Nine patients from the DC and SC groups reported soiling for more than twice per week. Sub-group analysis comparing patients with and without the entire sigmoid colon resected revealed worse functional outcomes in terms of the incidence of soiling (40.7 vs 22.2%, p = 0.05) and the BFS (14 vs 18, p = 0.04) in the former group. Anorectal manometry did not reveal any significant difference between the four groups, but a higher proportion of patients in the UR and LR groups appeared to have a normal sphincter resting pressure (DC vs SC vs UR vs LR = 62.5 vs 75.0 vs 85.7 vs 80.0%, p = 0.10).

CONCLUSION

Patients with short segment HSCR are not equal at all. HSCR patients with aganglionosis limited to the rectum without the need of removing the entire sigmoid colon have a better bowel control and overall functional score. Less bowel loss and colonic dissection maybe the underlying reasons. Although future studies with a larger sample size and a longer follow-up period are required to validate the results of this study, it has provided a new insight to the current understanding of short segment disease in HSCR.

摘要

背景/目的:短节段型先天性巨结肠(HSCR)的预后优于长节段型,但短节段的定义存在争议。本研究的目的是从解剖学角度确定与更好功能结局相关的疾病累及范围。

方法

这是一项回顾性多中心(n = 3)研究,对年龄≥3岁、因仅累及直肠乙状结肠的无神经节细胞症而接受经肛门拖出术的患者进行了回顾。通过查阅手术记录以及切除标本的组织病理学报告来获取疾病累及范围和肠切除情况。根据七项肠功能评分(BFS)标准(最高分 = 20分)进行临床评估。采用肛门直肠测压法进行测压评估。

结果

研究时间段从2003年开始,共研究了45例患者,评估时的中位年龄为52.0个月,手术时的中位年龄为3.0个月。根据正常活检结果的水平,将疾病累及情况分为乙状结肠上段-降结肠(DC)(n = 8)、乙状结肠(SC)(n = 12)、直肠上段(UR)(n = 14)和直肠下段(LR)(n = 11)。四组之间的评估年龄无显著差异。DC、SC、UR和LR组的中位BFS分别为13、15、17和17(p = 0.01)。DC组和SC组中有9例患者报告每周弄脏内裤超过两次。对切除和未切除整个乙状结肠的患者进行亚组分析,结果显示,在前一组中,就弄脏内裤的发生率(40.7%对22.2%,p = 0.05)和BFS(14对18,p = 0.04)而言,功能结局更差。肛门直肠测压显示四组之间无显著差异,但UR组和LR组中似乎有更高比例的患者括约肌静息压正常(DC组对SC组对UR组对LR组 = 62.5%对75.0%对85.7%对80.0%,p = 0.10)。

结论

短节段HSCR患者并非完全相同。无神经节细胞症仅限于直肠且无需切除整个乙状结肠的HSCR患者,其肠道控制能力和总体功能评分更好。较少的肠管丢失和结肠剥离可能是其潜在原因。尽管需要未来更大样本量和更长随访期的研究来验证本研究结果,但它为当前对HSCR短节段疾病的认识提供了新的见解。

相似文献

1
Are all patients with short segment Hirschsprung's disease equal? A retrospective multicenter study.所有短段型先天性巨结肠病患者都一样吗?一项回顾性多中心研究。
Pediatr Surg Int. 2018 Jan;34(1):47-53. doi: 10.1007/s00383-017-4202-4. Epub 2017 Oct 26.
2
Transanal one-stage endorectal pull-through for Hirschsprung's disease in infants and children.婴幼儿及儿童先天性巨结肠经肛门一期直肠内拖出术
J Pediatr Surg. 2003 Feb;38(2):184-7. doi: 10.1053/jpsu.2003.50039.
3
Evaluation of anorectal function after transanal one-stage endorectal pull through operation in children with Hirschsprung's disease.先天性巨结肠患儿经肛门一期直肠内拖出术后的肛门直肠功能评估
Zhongguo Dang Dai Er Ke Za Zhi. 2007 Jun;9(3):188-92.
4
Transanal endorectal pull-through for classic segment Hirschsprung's disease: with or without laparoscopic mobilization of the rectosigmoid?经肛门直肠内拖出术治疗经典型先天性巨结肠:是否联合腹腔镜辅助游离直肠乙状结肠?
J Pediatr Surg. 2013 Sep;48(9):1914-8. doi: 10.1016/j.jpedsurg.2013.04.025.
5
Modified transanal rectosigmoidectomy for Hirschsprung's disease: clinical and manometric results in the initial 20 cases.改良经肛门直肠乙状结肠切除术治疗先天性巨结肠:20例初治患者的临床及测压结果
J Pediatr Surg. 2003 Jul;38(7):1048-50. doi: 10.1016/s0022-3468(03)00189-1.
6
Transanal coloanal pull-through with a short muscular cuff for classic Hirschsprung's disease.经肛门结肠肛管拖出术联合短肌袖治疗典型先天性巨结肠症。
Eur J Pediatr Surg. 2003 Jun;13(3):181-6. doi: 10.1055/s-2003-41264.
7
Stooling patterns and colonic motility after transanal one-stage pull-through operation for Hirschsprung's disease in children.儿童先天性巨结肠经肛门一期拖出术后的排便模式和结肠动力
J Pediatr Surg. 2005 Nov;40(11):1766-72. doi: 10.1016/j.jpedsurg.2005.07.027.
8
Surgical management of recto-sigmoid Hirschsprung's disease.直肠乙状结肠型先天性巨结肠的手术治疗
Acta Chir Belg. 2012 Mar-Apr;112(2):126-30. doi: 10.1080/00015458.2012.11680810.
9
Effectiveness of various surgical methods in treatment of Hirschsprung's disease in children.各种手术方法治疗小儿先天性巨结肠症的疗效
Vojnosanit Pregl. 2016 Mar;73(3):246-50. doi: 10.2298/vsp140516002l.
10
[Transanal endorectal pull-through with short muscular cuff in the treatment of Hirschsprung disease. Preliminary study with 37 patients].[经肛门直肠内拖出术加短肌袖治疗先天性巨结肠。37例患者的初步研究]
Cir Pediatr. 2003 Oct;16(4):161-5.

引用本文的文献

1
Perioperative outcomes of neonatal versus delayed surgery for Hirschsprung disease: a nationwide retrospective cohort study in Japan.先天性巨结肠症新生儿手术与延迟手术的围手术期结局:日本一项全国性回顾性队列研究
Pediatr Surg Int. 2025 Jul 14;41(1):211. doi: 10.1007/s00383-025-06126-3.
2
Features of defecation dysfunction among patients with Hirschsprung disease in early childhood.幼儿期先天性巨结肠症患者排便功能障碍的特征。
BMC Gastroenterol. 2025 Jul 9;25(1):510. doi: 10.1186/s12876-025-04106-4.
3
Evaluation of Trans-Anal Endorectal Pull-Through Outcomes in Hirschsprung's Disease in Different Age Groups: A Comprehensive Systematic Review.

本文引用的文献

1
Manometric findings in relation to functional outcomes in different types of anorectal malformations.不同类型肛门直肠畸形的测压结果与功能结局的关系
J Pediatr Surg. 2017 Apr;52(4):563-568. doi: 10.1016/j.jpedsurg.2016.08.025. Epub 2016 Sep 2.
2
Long-term results of transanal pull-through for Hirschsprung's disease: a meta-analysis.先天性巨结肠经肛门拖出术的长期疗效:一项荟萃分析
Pediatr Surg Int. 2016 Aug;32(8):743-9. doi: 10.1007/s00383-016-3908-z. Epub 2016 Jul 6.
3
Hirschsprung's disease: A bridge for science and surgery.
不同年龄段先天性巨结肠经肛门直肠内拖出术治疗效果的评估:一项全面的系统性综述。
Arch Iran Med. 2024 Jul 1;27(7):392-399. doi: 10.34172/aim.28183.
4
Bowel function at preschool and early childhood age in children with long-segment Hirschsprung disease.长段型先天性巨结肠症患儿在学龄前及幼儿期的肠道功能
Eur J Pediatr. 2023 Mar;182(3):1251-1259. doi: 10.1007/s00431-023-04814-7. Epub 2023 Jan 12.
5
Roles of Enteric Neural Stem Cell Niche and Enteric Nervous System Development in Hirschsprung Disease.肠神经干细胞龛和肠神经系统发育在先天性巨结肠病中的作用。
Int J Mol Sci. 2021 Sep 7;22(18):9659. doi: 10.3390/ijms22189659.
6
Optimal timing for Soave primary pull-through in short-segment Hirschsprung disease: A meta-analysis.短节段先天性巨结肠 Soave 经肛门根治术的最佳时机:一项荟萃分析。
J Pediatr Surg. 2022 Apr;57(4):719-725. doi: 10.1016/j.jpedsurg.2021.07.007. Epub 2021 Jul 21.
7
Long-term outcomes and quality of life of patients with Hirschsprung disease: a systematic review and meta-analysis.先天性巨结肠症患者的长期预后和生活质量:系统评价和荟萃分析。
BMC Gastroenterol. 2020 Mar 12;20(1):67. doi: 10.1186/s12876-020-01208-z.
8
Congenital obstructive bowel anomalies presenting after neonatal age.新生儿期后出现的先天性肠梗阻异常。
Malawi Med J. 2019 Mar;31(1):77-81. doi: 10.4314/mmj.v31i1.13.
9
Risk factors for the development of post-operative enterocolitis in short segment Hirschsprung's disease.短段型先天性巨结肠术后发生小肠结肠炎的危险因素
Pediatr Surg Int. 2019 Feb;35(2):187-191. doi: 10.1007/s00383-018-4393-3. Epub 2018 Nov 1.
先天性巨结肠症:科学与外科手术之间的桥梁
J Pediatr Surg. 2016 Jan;51(1):18-22. doi: 10.1016/j.jpedsurg.2015.10.021. Epub 2015 Oct 21.
4
Anal endosonography and bowel function in patients undergoing different types of endorectal pull-through procedures for Hirschsprung disease.先天性巨结肠症患者接受不同类型经肛门直肠拖出术时的肛门内超声检查与肠道功能
J Pediatr Surg. 2015 Aug;50(8):1341-6. doi: 10.1016/j.jpedsurg.2014.12.024. Epub 2015 Jan 8.
5
Review of organic causes of fecal incontinence in children: evaluation and treatment.儿童粪便失禁的有机病因综述:评估与治疗。
Expert Rev Gastroenterol Hepatol. 2013 Sep;7(7):657-67. doi: 10.1586/17474124.2013.832500.
6
Hirschsprung disease.先天性巨结肠症。
Curr Opin Pediatr. 2013 Jun;25(3):368-74. doi: 10.1097/MOP.0b013e328360c2a0.
7
Bowel function and fecal continence after Soave's trans-anal endorectal pull-through for Hirschsprung's disease: a local experience.经肛门直肠内拖出术治疗先天性巨结肠术后的肠功能和粪便控制:本地经验。
Updates Surg. 2012 Jun;64(2):113-8. doi: 10.1007/s13304-012-0140-9. Epub 2012 Mar 6.
8
Defecation disorders in children after surgery for Hirschsprung disease.先天性巨结肠症患儿术后排便障碍。
J Pediatr Gastroenterol Nutr. 2011 Jul;53(1):75-9. doi: 10.1097/MPG.0b013e318212eb53.
9
Bowel function and gastrointestinal quality of life among adults operated for Hirschsprung disease during childhood: a population-based study.儿童时期接受巨结肠症手术的成年人的肠道功能和胃肠道生活质量:一项基于人群的研究。
Ann Surg. 2010 Dec;252(6):977-81. doi: 10.1097/SLA.0b013e3182018542.
10
Hirschsprung's disease.先天性巨结肠症
Semin Pediatr Surg. 2010 Aug;19(3):194-200. doi: 10.1053/j.sempedsurg.2010.03.004.