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泄殖腔缺损的重建:转换手术——一种新方法。

Reconstruction of Cloacal Defect: Switch Operation - A New Approach.

作者信息

Basu Ashoke Kumar, Basu Kalyani Saha, Bhaumik Kuntal, Basu Jyotsna, Aanad Abhishek

机构信息

Department of Pediatric Surgery, Institute of Child Health, Kolkata, India.

Department of Pediatric Surgery, Nil Ratan Sarkar Medical College and Hospital, Kolkata, India.

出版信息

J Indian Assoc Pediatr Surg. 2024 Jul-Aug;29(4):334-339. doi: 10.4103/jiaps.jiaps_239_23. Epub 2024 Jul 6.

DOI:10.4103/jiaps.jiaps_239_23
PMID:39149440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11324082/
Abstract

INTRODUCTION

Reconstruction of a cloacal defect in a girl is often difficult and complicated.[1] This is most often done either by the sacro-perineal route or through the posterior sagittal route.[2] The procedures may involve total mobilization of the cloaca with or without the creation of a lower vagina with the help of a loop of vascularized bowel.[3] In our approach, such defects can be corrected using the lower anorectum for the creation of a lower vagina and abdominoperineal pull-through of the proximal divided bowel. This method can be used both in short and long common channel cloaca.

MATERIALS AND METHODS

We have used this procedure in one patient of posterior cloaca and four patients of anterior cloaca. These operations were done in patients of 1 year and 6 months to 4 years. Only one patient is waiting for the closure of the colostomy.

RESULTS

In all the cases, the urethra, the vagina, and the anus were successfully separated.

CONCLUSION

This operation restores normal pelvic anatomy and physiology with minimal mutilation of the pelvic floor.

摘要

引言

女童泄殖腔缺损的重建手术通常困难且复杂。[1] 最常通过骶会阴途径或后矢状途径进行。[2] 手术可能包括在有或没有带血管蒂肠袢辅助下完全游离泄殖腔以形成低位阴道。[3] 在我们的手术方法中,此类缺损可利用低位直肠来形成低位阴道,并通过腹会阴拖出近端离断肠管进行修复。该方法可用于短和长共同通道型泄殖腔。

材料与方法

我们已将此手术应用于1例后泄殖腔患者和4例前泄殖腔患者。这些手术在年龄为1岁6个月至4岁的患者中进行。仅1例患者等待结肠造口关闭。

结果

在所有病例中,尿道、阴道和肛门均成功分离。

结论

该手术能以对盆底最小限度的毁损恢复正常的盆腔解剖结构和生理功能。

相似文献

1
Reconstruction of Cloacal Defect: Switch Operation - A New Approach.泄殖腔缺损的重建:转换手术——一种新方法。
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2
Surgical management of cloacal malformations: a review of 339 patients.泄殖腔畸形的外科治疗:339例患者的回顾
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本文引用的文献

1
Posterior Cloacal Variant with Clitorolabial Transposition and a Rectoperineal Fistula.伴有阴蒂阴唇转位及直肠会阴瘘的后泄殖腔变异型
European J Pediatr Surg Rep. 2021 Jan;9(1):e46-e49. doi: 10.1055/s-0041-1728724. Epub 2021 May 18.
2
A unique defect - persistent posterior cloaca: An example of staged genito-urinary and digestive tract reconstruction with an alternative vaginal creation using the urinary bladder wall.
Int J Urol. 2017 Jun;24(6):468-471. doi: 10.1111/iju.13332. Epub 2017 May 6.
3
Reverse (posterior) cloaca with congenital rectal stenosis and pseudohermaphrodism: a rare entity with rare association.伴有先天性直肠狭窄和假性两性畸形的反向(后位)泄殖腔:一种罕见的实体,伴有罕见的关联。
BMJ Case Rep. 2010 Nov 26;2010:bcr0620103071. doi: 10.1136/bcr.06.2010.3071.
4
Posterior cloaca--further experience and guidelines for the treatment of an unusual anorectal malformation.后肛——一种不常见的肛门直肠畸形的治疗经验及指南。
J Pediatr Surg. 2010 Jun;45(6):1234-40. doi: 10.1016/j.jpedsurg.2010.02.095.
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Cloacal malformations: lessons learned from 490 cases.泄殖腔畸形:从490例病例中吸取的经验教训。
Semin Pediatr Surg. 2010 May;19(2):128-38. doi: 10.1053/j.sempedsurg.2009.11.012.
6
Bladder function after total urogenital mobilization for persistent cloaca.持续性泄殖腔畸形患者经全泌尿生殖系统游离后的膀胱功能
J Urol. 2009 Nov;182(5):2455-9. doi: 10.1016/j.juro.2009.07.052. Epub 2009 Sep 17.
7
Surgical management of cloacal malformations: a review of 339 patients.泄殖腔畸形的外科治疗:339例患者的回顾
J Pediatr Surg. 2004 Mar;39(3):470-9; discussion 470-9. doi: 10.1016/j.jpedsurg.2003.11.033.
8
Long-term urological outcome of patients presenting with persistent cloaca.患有持续性泄殖腔畸形患者的长期泌尿系统预后
J Urol. 2002 Oct;168(4 Pt 2):1859-62; discussion 1862. doi: 10.1097/01.ju.0000030712.17096.0d.
9
Cloaca, the most severe degree of imperforate anus: experience with 195 cases.泄殖腔畸形,最严重程度的肛门闭锁:195例病例经验
Ann Surg. 1998 Sep;228(3):331-46. doi: 10.1097/00000658-199809000-00006.
10
Posterior cloaca: a unique defect.后泄殖腔:一种独特的缺陷。
J Pediatr Surg. 1998 Mar;33(3):407-12. doi: 10.1016/s0022-3468(98)90079-3.