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先天性巨结肠再次拖出术的经验

Experience with the Redo Pull-Through for Hirschsprung's Disease.

作者信息

Gupta Devendra K, Khanna Kashish, Sharma Shilpa

机构信息

Department of Pediatric Surgery, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Indian Assoc Pediatr Surg. 2019 Jan-Mar;24(1):45-51. doi: 10.4103/jiaps.JIAPS_52_18.

DOI:10.4103/jiaps.JIAPS_52_18
PMID:30686887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6322179/
Abstract

AIM

This study aims to evaluate the need of Redo pull-through (Re PT) procedures for Hirschsprung's disease (HD) and suggest preventive strategies.

MATERIALS AND METHODS

Patients who underwent redo procedures for HD from 1980 to 2016 by a single surgeon were retrospectively reviewed.

RESULTS

Of 167 patients operated for HD, 32 underwent Re PT; 7 were previously operated by the same surgeon, while 25 were referred from outside. Indication for Re PT included residual disease including the rectal pouch following-Duhamel (12), false-negative biopsy (3), retraction of bowel (5), anorectal stricture (2), bowel twist (1), cuff inversion (2), postmyectomy continued symptoms after primary PT (1), fecal fistula (1), Re PT after surgery for adhesive intestinal obstruction (3), bleeding (1), and combination of causes, including scarred perineum (1). Age at follow-up ranged from 2.5 to 26 years. Proximal diversion was performed in 19 and 14 underwent open Scott Boley's/Soave PT and 5 ileoanal anastomosis. Of the remaining, nondiverted 13 patients, 5 underwent transanal endorectal PT and 8 underwent PT of colostomy.

CONCLUSIONS

Most patients of Re PT came after an initial Duhamel's procedure. Retraction of bowel, inversion of cuff, twist, distal bowel stricture, and perianal fibrosis were found after Scott Boley procedure. Proper planning with an initial diversion, nutritional buildup, barium study evaluation, frozen section facility, experienced pathologist, and an expert surgeon are prerequisites for a successful outcome after an initial as well as Re PT.

摘要

目的

本研究旨在评估先天性巨结肠(HD)再次拖出术(Re PT)的必要性并提出预防策略。

材料与方法

回顾性分析1980年至2016年由同一位外科医生为HD患者实施再次手术的病例。

结果

167例接受HD手术的患者中,32例行Re PT;7例曾由同一位外科医生手术,25例为外院转诊。Re PT的指征包括残留病变,如Duhamel术后直肠盲袋(12例)、活检假阴性(3例)、肠管回缩(5例)、肛门直肠狭窄(2例)、肠扭转(1例)、袖口内翻(2例)、初次PT后肌切除术后仍有症状(1例)、粪瘘(1例)、粘连性肠梗阻手术后行Re PT(3例)、出血(1例)以及多种原因并存,包括会阴瘢痕(1例)。随访年龄范围为2.5至26岁。19例行近端造瘘,14例行开放式Scott Boley/Soave PT,5例行回肠肛管吻合术。其余13例未行造瘘的患者中,5例行经肛门直肠内PT,8例行结肠造口PT。

结论

多数Re PT患者初次手术为Duhamel术式。Scott Boley术后发现肠管回缩、袖口内翻、扭转、远端肠管狭窄及肛周纤维化。初次手术及Re PT成功的前提是进行合理规划,包括初次造瘘、营养支持、钡剂造影评估、冰冻切片检查、经验丰富的病理学家及专业的外科医生。

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本文引用的文献

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Ann Surg. 2017 Mar;265(3):622-629. doi: 10.1097/SLA.0000000000001695.
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Redo pullthrough for Hirschsprung disease.重复行先天性巨结肠拖出术。
Pediatr Surg Int. 2017 Apr;33(4):455-460. doi: 10.1007/s00383-016-4045-4. Epub 2016 Dec 31.
3
Long-term outcome of bowel function for 110 consecutive cases of Hirschsprung's disease: Comparison of the abdominal approach with transanal approach more than 30years in a single institution - is the transanal approach truly beneficial for bowel function?
Children (Basel). 2023 Aug 30;10(9):1475. doi: 10.3390/children10091475.
4
Laparoscopic restorative proctocolectomy with ileal-J-pouch anal canal anastomosis without diverting ileostomy for total colonic and extensive aganglionosis is safe and feasible with combined Lugol's iodine staining technique and indocyanine green fluorescence angiography.对于全结肠及广泛性无神经节细胞症,采用卢戈氏碘染色技术和吲哚菁绿荧光血管造影术联合进行腹腔镜保留直肠全结肠切除术并回肠J袋肛管吻合术(不做转流性回肠造口术)是安全可行的。
Front Pediatr. 2023 Jan 6;10:1090336. doi: 10.3389/fped.2022.1090336. eCollection 2022.
5
Laparoscopic vs. Transabdominal Treatment for Overflow Fecal Incontinence Due to Residual Aganglionosis or Transition Zone Pathology in Hirschsprung's Disease Reoperation.腹腔镜与经腹治疗先天性巨结肠再手术中因残留无神经节症或移行区病变导致的充溢性大便失禁
Front Pediatr. 2021 Apr 27;9:600316. doi: 10.3389/fped.2021.600316. eCollection 2021.
6
Division of Long Residual Spur after Duhamel's Pull through with Endo-GIA Stapler under Colonoscopic Guidance.结肠镜引导下使用内镜切割吻合器行杜哈梅尔拖出术后长残留盲端的处理
J Indian Assoc Pediatr Surg. 2021 Jan-Feb;26(1):69-70. doi: 10.4103/jiaps.JIAPS_281_20. Epub 2021 Jan 11.
110例先天性巨结肠连续病例的肠道功能长期预后:单一机构30多年来经腹手术与经肛门手术的比较——经肛门手术对肠道功能真的有益吗?
J Pediatr Surg. 2016 Dec;51(12):2010-2014. doi: 10.1016/j.jpedsurg.2016.09.029. Epub 2016 Oct 29.
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Functional outcomes in Hirschsprung disease: A single institution's 12-year experience.先天性巨结肠症的功能结局:一家机构的12年经验
J Pediatr Surg. 2017 Feb;52(2):277-280. doi: 10.1016/j.jpedsurg.2016.11.023. Epub 2016 Nov 14.
5
European Paediatric Surgeons' Association Survey on the Management of Hirschsprung Disease.欧洲小儿外科医生协会关于先天性巨结肠症治疗的调查
Eur J Pediatr Surg. 2017 Feb;27(1):96-101. doi: 10.1055/s-0036-1593991. Epub 2016 Nov 29.
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Reoperative surgery for Hirschsprung disease.先天性巨结肠的再次手术
Semin Pediatr Surg. 2012 Nov;21(4):354-63. doi: 10.1053/j.sempedsurg.2012.07.011.
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Redo pull-through in Hirschsprung's [corrected] disease for obstructive symptoms due to residual aganglionosis and transition zone bowel.先天性巨结肠症患儿因残留无神经节细胞区和移行区肠段导致梗阻症状,行 redo 经肛门拖出术。 (注:原文中 [corrected] 为作者勘误,提示原 Hirschsprung's disease 拼写错误,正确拼写应为 Hirschsprung's disease。)
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Semin Pediatr Surg. 2010 May;19(2):146-53. doi: 10.1053/j.sempedsurg.2009.11.013.