• 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

膀胱矢状隔重复和后尿道重复合并先天性巨结肠:一例病例报告及文献复习。

Sagittal septum duplication of bladder and duplication of posterior urethra combined with congenital megacolon: a case report and literature review.

机构信息

Department of Radiology, Medical Imaging Center of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, China.

Department of Urology, Affiliated Hospital of Zunyi Medical University, Zunyi, 563003, China.

出版信息

BMC Urol. 2024 Jan 3;24(1):9. doi: 10.1186/s12894-023-01395-3.

DOI:10.1186/s12894-023-01395-3
PMID:38172803
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10765677/
Abstract

BACKGROUND

Duplication of the bladder with duplication of the posterior urethra is a relatively rare congenital malformation. Cases of sagittal septum duplication of the bladder with duplication of the posterior urethra have rarely been reported. Furthermore, the combination thereof with congenital megacolon is rare.

CASE PRESENTATION

A 21-year-old male was admitted to our hospital because of frequent urination for two months. He presented to another hospital first with frequent urination and underwent computed tomography (CT) and testicular biopsy. Anti-inflammatory therapy was administered by the doctor to the patient. For further diagnosis and treatment, the patient went to the outpatient department in our hospital on June 6, 2022. After admission, the patient underwent ultrasound, CT, MRI, cystoscopy, and other related examinations and tests. The examination results suggested that the patient had duplication of the bladder with duplication of the posterior urethra. In addition, the patient's mother reported that he had suffered from long-term constipation with abdominal distension before the age of 5 years. At the time, he was admitted to the local hospital and was diagnosed with congenital megacolon based on the relevant examinations. After the patient was diagnosed with duplication of bladder and urethra, the doctor recommended surgical treatment to the patient. However, he considered that he only had frequent urination symptoms, and chose conservative treatment rather than to undergo surgical treatment. Thus, the doctor prescribed anti-inflammatory treatment. Four months later, the patient reported that frequent urination symptoms persisted, and was also considering fertility-related problems. The outpatient follow-up will be continued.

CONCLUSIONS

In this article, we summarize the imaging findings of duplication of the bladder with duplication of the posterior urethra and propose the advantages and disadvantages of each type of imaging examination. We also review the relevant literature on cases of bladders with duplication of the posterior urethra. The related differential diagnosis is summarized, and the significance of guiding clinical treatment and diagnosis is discussed.

摘要

背景

膀胱重复合并后尿道重复是一种相对罕见的先天性畸形。膀胱矢状隔重复合并后尿道重复的病例很少有报道。此外,合并先天性巨结肠更为罕见。

病例介绍

一名 21 岁男性因尿频 2 个月入院。他最初因尿频就诊于另一家医院,接受了 CT 和睾丸活检。医生给予患者抗炎治疗。为了进一步诊断和治疗,患者于 2022 年 6 月 6 日到我院门诊就诊。入院后,患者进行了超声、CT、MRI、膀胱镜等相关检查和检验。检查结果提示患者患有膀胱重复合并后尿道重复。此外,患者的母亲报告称,他在 5 岁前长期便秘伴腹胀,当时他被送往当地医院,根据相关检查被诊断为先天性巨结肠。在患者被诊断为膀胱和尿道重复后,医生向患者推荐了手术治疗。然而,他认为自己只有尿频症状,选择了保守治疗而不是手术治疗。因此,医生开了抗炎治疗。4 个月后,患者报告尿频症状持续存在,也在考虑与生育有关的问题。将继续门诊随访。

结论

本文总结了膀胱重复合并后尿道重复的影像学表现,并提出了各种影像学检查的优缺点。我们还回顾了膀胱后尿道重复的相关病例文献。总结了相关的鉴别诊断,并讨论了对指导临床治疗和诊断的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/f99a7bd6322c/12894_2023_1395_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/2aeae2f425e9/12894_2023_1395_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/d262c13db540/12894_2023_1395_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/640d135c41a9/12894_2023_1395_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/4e9b8ee5040f/12894_2023_1395_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/f99a7bd6322c/12894_2023_1395_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/2aeae2f425e9/12894_2023_1395_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/d262c13db540/12894_2023_1395_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/640d135c41a9/12894_2023_1395_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/4e9b8ee5040f/12894_2023_1395_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29cc/10765677/f99a7bd6322c/12894_2023_1395_Fig5_HTML.jpg

相似文献

1
Sagittal septum duplication of bladder and duplication of posterior urethra combined with congenital megacolon: a case report and literature review.膀胱矢状隔重复和后尿道重复合并先天性巨结肠:一例病例报告及文献复习。
BMC Urol. 2024 Jan 3;24(1):9. doi: 10.1186/s12894-023-01395-3.
2
Complete duplication of bladder and urethra in coronal plane with no other anomalies: case report with review of the literature.膀胱和尿道在冠状面完全重复且无其他异常:病例报告并文献复习
Urology. 2005 Feb;65(2):388. doi: 10.1016/j.urology.2004.08.043.
3
Complete duplication of bladder and urethra in a sagittal plane in a male infant: case report and literature review.男性婴儿膀胱和尿道矢状面完全重复畸形:病例报告及文献复习
J Pediatr Urol. 2008 Aug;4(4):255-9. doi: 10.1016/j.jpurol.2008.02.001. Epub 2008 Apr 14.
4
Unusual case of bladder duplication: complete duplication in coronal plane with single urethra and no associated anomalies.膀胱重复畸形的罕见病例:冠状面完全重复,伴有单一尿道且无相关异常。
Urology. 2006 Nov;68(5):1121.e1-3. doi: 10.1016/j.urology.2006.06.002.
5
Complete duplication of the bladder and urethra in the coronal plane: case report with review of the literature.膀胱和尿道在冠状面完全重复:病例报告并文献复习
Urol Int. 2013;90(1):118-20. doi: 10.1159/000339922. Epub 2012 Aug 3.
6
Endourological management in a newborn with incomplete bladder duplication.新生儿不完全膀胱重复畸形的腔内泌尿外科处理。
J Pediatr Urol. 2013 Feb;9(1):e19-21. doi: 10.1016/j.jpurol.2011.11.015. Epub 2012 Jul 7.
7
Urethral duplication--a wide spectrum of anomalies.尿道重复畸形——一种广泛的异常。
J Pediatr Urol. 2013 Dec;9(6 Pt B):1064-71. doi: 10.1016/j.jpurol.2013.03.006. Epub 2013 Apr 24.
8
Complete bladder and urethral duplication with normal urodynamic function associated with visceral sequestration.完全性膀胱及尿道重复,伴有正常尿动力学功能及内脏隔离。
Urology. 2012 Apr;79(4):906-7. doi: 10.1016/j.urology.2011.08.037. Epub 2011 Oct 15.
9
Unusual case of coronal complete bladder duplication associated with rectoprostatic fistula to duplicated prostatic urethra.伴有直肠前列腺瘘至重复前列腺尿道的冠状完全膀胱重复罕见病例。
Pediatr Surg Int. 2018 Jan;34(1):105-108. doi: 10.1007/s00383-017-4200-6. Epub 2017 Oct 13.
10
Complete duplication of bladder and urethra in the coronal plane in a girl: case report and review of the literature.一名女孩膀胱和尿道在冠状面完全重复:病例报告及文献复习
Pediatr Radiol. 1999 Mar;29(3):171-3. doi: 10.1007/s002470050564.

引用本文的文献

1
Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report.膀胱不完全重复畸形的迟发性表现:一例意外误诊的罕见病例报告
Urol Case Rep. 2025 May 19;61:103074. doi: 10.1016/j.eucr.2025.103074. eCollection 2025 Jul.
2
Surgical management of rare complete duplicated urethra with epispadias (Effmann Type Ⅱ A1): A novel approach.罕见的完全重复尿道伴尿道上裂(埃夫曼Ⅱ A1型)的手术治疗:一种新方法。
Urol Case Rep. 2025 May 12;61:103063. doi: 10.1016/j.eucr.2025.103063. eCollection 2025 Jul.

本文引用的文献

1
Bladder duplication in infant girls: role of imaging in two rare cases with variants of a complete sagittal septum.婴儿女孩的膀胱重复畸形:两种罕见病例中完全矢状隔变异的影像学作用。
Pediatr Radiol. 2023 May;53(5):1033-1038. doi: 10.1007/s00247-023-05603-y. Epub 2023 Jan 23.
2
Papers presented at the fall 2020 Pediatric Urologic Oncology Work Group of the Societies of Pediatric Urology meetingBladder Duplication in a Setting of VACTER Association.在2020年秋季小儿泌尿外科协会小儿泌尿肿瘤学工作组会议上发表的论文:VACTER综合征合并膀胱重复畸形
Urology. 2021 Jul;153:307-311. doi: 10.1016/j.urology.2021.02.002. Epub 2021 Feb 9.
3
Bladder Duplication - A Case Series.
膀胱重复畸形 - 病例系列
Urology. 2021 Mar;149:199-205. doi: 10.1016/j.urology.2020.11.001. Epub 2020 Nov 13.
4
Detection of Incomplete Bladder Duplication by SPECT/CT.通过SPECT/CT检测不完全性膀胱重复畸形
J Nucl Med Technol. 2020 Dec;48(4):381-383. doi: 10.2967/jnmt.120.246801. Epub 2020 Jul 24.
5
Case-report: A rare cause of an intra-abdominal mass.病例报告:腹腔内肿块的罕见病因。
Int J Surg Case Rep. 2020;67:278-281. doi: 10.1016/j.ijscr.2020.01.006. Epub 2020 Feb 20.
6
CT and MRI features of tumors and tumor-like lesions in the abdominal wall.腹壁肿瘤及肿瘤样病变的CT和MRI特征
Quant Imaging Med Surg. 2019 Nov;9(11):1820-1839. doi: 10.21037/qims.2019.09.03.
7
Bilateral Obstructive Uropathy Caused by Congenital Bladder Diverticulum Presenting as Hypertensive Retinopathy.先天性膀胱憩室致双侧梗阻性尿路病变合并高血压性视网膜病变
J Korean Med Sci. 2018 Feb 19;33(8):e54. doi: 10.3346/jkms.2018.33.e54.
8
Spontaneous rupture of urinary bladder diverticulum with pseudo-acute renal failure.膀胱憩室自发性破裂伴假性急性肾衰竭。
Intern Emerg Med. 2018 Jun;13(4):619-622. doi: 10.1007/s11739-018-1796-z. Epub 2018 Jan 30.
9
Imaging of urethral stricture disease.尿道狭窄疾病的影像学检查
Transl Androl Urol. 2015 Feb;4(1):2-9. doi: 10.3978/j.issn.2223-4683.2015.02.03.
10
Systematic stereoscopic analyses for cloacal development: The origin of anorectal malformations.泄殖腔发育的系统立体分析:肛门直肠畸形的起源
Sci Rep. 2015 Sep 10;5:13943. doi: 10.1038/srep13943.