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先天性囊状结肠:两种治疗方式的对比研究。

Congenital pouch colon: A comparative study between two modalities of management.

机构信息

Department of Pediatric Surgery, SVP Post Graduate Institute of Pediatrics, SCB Medical College, Cuttack, Odisha, India.

出版信息

Afr J Paediatr Surg. 2021 Jan-Mar;18(1):33-38. doi: 10.4103/ajps.AJPS_53_20.

DOI:10.4103/ajps.AJPS_53_20
PMID:33595539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8109753/
Abstract

BACKGROUND

Congenital pouch colon (CPC) is an unusual anomaly with an unique geographical distribution. The aim of this study was to find out the incidence of CPC among anorectal malformation (ARM) cases in our institute and to compare the outcome between conventional three-staged surgery versus two-staged management approach.

MATERIALS AND METHODS

This study was conducted in the department of pediatric surgery over a period of 7 years from 1 April 2013 to 31 March 2020.

RESULTS

Out of 754 cases of ARMs, 43 cases of CPC were detected. The incidence of pouch colon among patients with high ARMs was found to be 7.6% with a male predominance (M:F = 4.4:1). The anomaly was diagnosed in 72% of our patients preoperatively and Type IV variety was the most common intra-operative finding. The survival after initial hospitalisation was 82% and 88% in three-stage and two-stage surgical procedures, respectively. However, the final clinical outcome after the completion of all stages of surgery and follow-up was better in two-staged approach (54% vs. 47%).

CONCLUSION

Although, CPC is a rare anomaly, the incidence in our institute is 7.6% among high ARM cases. As compared to conventional three-staged surgery, the two-staged management approach has the advantage of better survival and decreased morbidity.

摘要

背景

先天性囊状结肠(CPC)是一种罕见的异常,具有独特的地理分布。本研究旨在探讨我院肛门直肠畸形(ARM)病例中 CPC 的发生率,并比较传统的三阶段手术与两阶段治疗方法的结果。

材料与方法

这项研究是在 2013 年 4 月 1 日至 2020 年 3 月 31 日期间在小儿外科部门进行的,为期 7 年。

结果

在 754 例 ARM 中,发现 43 例 CPC。高位 ARM 患者中囊状结肠的发生率为 7.6%,男性占优势(M:F=4.4:1)。72%的患者在术前被诊断出患有该疾病,且最常见的术中发现是 IV 型。初次住院后的存活率分别为三阶段手术和两阶段手术的 82%和 88%。然而,在完成所有阶段的手术和随访后,两阶段方法的最终临床结局更好(54%比 47%)。

结论

尽管 CPC 是一种罕见的异常,但在我院高位 ARM 病例中的发生率为 7.6%。与传统的三阶段手术相比,两阶段治疗方法具有更好的生存率和降低发病率的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/5b4803c37eda/AJPS-18-33-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/6585a67d0b4c/AJPS-18-33-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/8b7fe2f265ba/AJPS-18-33-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/3f8e1cf3c330/AJPS-18-33-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/5b4803c37eda/AJPS-18-33-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/6585a67d0b4c/AJPS-18-33-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/8b7fe2f265ba/AJPS-18-33-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/3f8e1cf3c330/AJPS-18-33-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c065/8109753/5b4803c37eda/AJPS-18-33-g004.jpg

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本文引用的文献

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Whole exome sequencing reveals rare variants linked to congenital pouch colon.全外显子组测序揭示与先天性袋状结肠相关的罕见变异。
Sci Rep. 2018 Apr 27;8(1):6646. doi: 10.1038/s41598-018-24967-y.
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Congenital Pouch Colon.先天性袋状结肠
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Congenital pouch colon in girls: Genitourinary abnormalities and their management.女童先天性袋状结肠:泌尿生殖系统异常及其处理
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Two-staged management for all types of congenital pouch colon.针对所有类型先天性袋状结肠的两阶段管理。
Afr J Paediatr Surg. 2013 Jan-Apr;10(1):17-23. doi: 10.4103/0189-6725.109378.
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Congenital pouch colon: Increasing association with low anorectal anomalies.先天性袋状结肠:与低位肛肠畸形的关联日益增加。
J Indian Assoc Pediatr Surg. 2009 Oct;14(4):218-20. doi: 10.4103/0971-9261.59606.
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Management of congenital pouch colon based on the Saxena-Mathur classification.基于萨克森纳-马图尔分类法的先天性袋状结肠的管理
J Pediatr Surg. 2009 May;44(5):962-6. doi: 10.1016/j.jpedsurg.2009.01.035.
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Technique and long-term results of coloplasty for congenital short colon.先天性短结肠结肠成形术的技术与长期疗效
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Classification of congenital pouch colon based on anatomic morphology.基于解剖形态学的先天性袋状结肠分类
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Congenital pouch colon syndrome: a report of 17 cases.先天性袋状结肠综合征:17例报告
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Single-stage management of all pouch colon (anorectal malformation) in newborns.新生儿所有袋状结肠(肛门直肠畸形)的一期管理。
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