• 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

先天性长直肠阴囊瘘：一种罕见的变异型。

A congenital long rectoscrotal fistula: A rare variant.

作者信息

Shripati Aihole Jayalaxmi

机构信息

Department of Paediatric Surgery, IGICH, Bangalore, Karnataka, India.

出版信息

Radiol Case Rep. 2022 Jul 27;17(10):3511-3514. doi: 10.1016/j.radcr.2022.07.005. eCollection 2022 Oct.

DOI:10.1016/j.radcr.2022.07.005
PMID:35912295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9334912/
Abstract

Congenital rectoscrotal fistula is a rare variant of anorectal malformations (ARM) as per pena classification. Its nomenclature as well as the management, obviously has not been discussed in literature so far. One such rare case and its management in a male neonate have been discussed here. Non or occasionally deflating congenital recto scrotal fistula has to be managed like an intermediate ARM.

摘要

根据佩纳分类法，先天性直肠阴囊瘘是一种罕见的肛门直肠畸形（ARM）变体。到目前为止，其命名以及治疗方法在文献中显然尚未被讨论过。本文讨论了一名男性新生儿的此类罕见病例及其治疗方法。无或偶尔不排气的先天性直肠阴囊瘘必须像治疗中度肛门直肠畸形一样进行处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/b6c3c4e854ff/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/ac4dc5fa066b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/b6c3c4e854ff/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/ac4dc5fa066b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/b6c3c4e854ff/gr2.jpg

相似文献

1
A congenital long rectoscrotal fistula: A rare variant.先天性长直肠阴囊瘘：一种罕见的变异型。
Radiol Case Rep. 2022 Jul 27;17(10):3511-3514. doi: 10.1016/j.radcr.2022.07.005. eCollection 2022 Oct.
2
Case Report: A Case Series of Rare High-Type Anorectal Malformations With Perineal Fistula: Beware of Urethral Involvement.病例报告：一系列罕见的伴有会阴瘘的高位型肛肠畸形病例：谨防尿道受累。
Front Surg. 2021 Jul 15;8:693587. doi: 10.3389/fsurg.2021.693587. eCollection 2021.
3
A comparison of laparoscopic-assisted (LAARP) and posterior sagittal (PSARP) anorectoplasty in the outcome of intermediate and high anorectal malformations.腹腔镜辅助（LAARP）与后矢状（PSARP）肛门直肠成形术治疗中高位肛门直肠畸形疗效的比较
S Afr J Surg. 2011 Mar 14;49(1):39-43.
4
[Rare anorectal malformation with recto-uretrobulbar fistula: about a case].[罕见的伴有直肠-尿道球部瘘的肛门直肠畸形：病例报告]
Pan Afr Med J. 2017 Nov 22;28:255. doi: 10.11604/pamj.2017.28.255.14299. eCollection 2017.
5
Diversities of H-type anorectal malformation: a systematic review on a rare variant of the Krickenbeck classification.H型肛门直肠畸形的多样性：对克里肯贝克分类法罕见变体的系统评价
Pediatr Surg Int. 2017 Jan;33(1):3-13. doi: 10.1007/s00383-016-3982-2. Epub 2016 Oct 1.
6
Laparoscopic-assisted PSARP - the advantages of combining both techniques for the treatment of anorectal malformations with recto-bladderneck or high prostatic fistulas.腹腔镜辅助 PSARP-联合两种技术治疗直肠膀胱颈或高位前列腺瘘肛门直肠畸形的优势。
J Pediatr Surg. 2013 Feb;48(2):367-71. doi: 10.1016/j.jpedsurg.2012.11.019.
7
Congenital anomaly rectified at birth: one-stage single-incision laparoscopic-assisted anorectoplasty for newborns with anorectal malformations and recto-urethral fistula.出生时矫正的先天性畸形：一期单切口腹腔镜辅助肛门直肠成形术治疗新生儿肛门直肠畸形合并直肠尿道瘘
Surg Endosc. 2016 Nov;30(11):5156-5164. doi: 10.1007/s00464-016-4841-x. Epub 2016 Mar 11.
8
Single-stage surgical correction of anorectal malformation associated with rectourinary fistula in male neonates.男性新生儿肛门直肠畸形合并直肠尿道瘘的一期手术矫正
J Neonatal Surg. 2013 Jan 1;2(1):3. eCollection 2013 Jan-Mar.
9
Congenital rectovaginal fistula with anorectal agenesis: A rare anorectal malformation.先天性直肠阴道瘘合并肛门直肠闭锁：一种罕见的肛门直肠畸形。
Int J Pediatr Adolesc Med. 2017 Dec;4(4):138-140. doi: 10.1016/j.ijpam.2017.08.003. Epub 2017 Dec 16.
10
OUTCOMES OF POSTERIOR SAGITTAL ANORECTOPLASTY FOR HIGH ANORECTAL MALFORMATION IN BENIN CITY, NIGERIA.尼日利亚贝宁城高肛门直肠畸形的后矢状入路肛门直肠成形术的治疗结果
J West Afr Coll Surg. 2016 Jan-Mar;6(1):16-30.

本文引用的文献

1
The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines.SCARE 2020 指南：更新共识手术病例报告（SCARE）指南。
Int J Surg. 2020 Dec;84:226-230. doi: 10.1016/j.ijsu.2020.10.034. Epub 2020 Nov 9.
2
Anorectal malformations.肛门直肠畸形
Orphanet J Rare Dis. 2007 Jul 26;2:33. doi: 10.1186/1750-1172-2-33.
3
Analysis of 1,992 patients with anorectal malformations over the past two decades in Japan. Steering Committee of Japanese Study Group of Anorectal Anomalies.对日本过去二十年里1992例肛门直肠畸形患者的分析。日本肛门直肠畸形研究组指导委员会。
J Pediatr Surg. 1999 Mar;34(3):435-41. doi: 10.1016/s0022-3468(99)90494-3.
4
[Rare anorectal malformations. Intermediate-type anal agenesis with a rectocutaneous fistula].[罕见的肛肠畸形。伴有直肠皮肤瘘的中间型肛门闭锁]
Minerva Chir. 1998 Nov;53(11):935-8.
5
Rectoperineal fistula in newborn boys.男新生儿直肠会阴瘘
J Pediatr Surg. 1994 Apr;29(4):536-7. doi: 10.1016/0022-3468(94)90085-x.