• 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

睾丸横过异位合并苗勒管永存综合征:手术中的重大发现。

Transverse testicular ectopia with persistent Mullerian duct syndrome: an operative eureka.

作者信息

Mukhtar Muhammad Umer, Niazi Shehryar Ahmed Khan, Sarwar Muhammad Zeeshan, Naqi Syed Asghar

机构信息

King Edward Medical University/Mayo Hospital, Lahore, Pakistan.

Department of Surgery, King Edward Medical University/Mayo Hospital, Lahore, Pakistan.

出版信息

Int J Surg Case Rep. 2020;71:338-340. doi: 10.1016/j.ijscr.2020.04.035. Epub 2020 May 11.

DOI:10.1016/j.ijscr.2020.04.035
PMID:32492648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7264951/
Abstract

INTRODUCTION

Transverse Testicular Ectopia (TTE) is a rare entity in which both testes descend on the same side, and can be found in ectopic locations. When present with Persistent Mullerian Duct Syndrome (PMDS), a yet rarer entity, the persistence of Mullerian duct derivatives i.e. fallopian tubes, uterus, cervix and upper two-thirds of vagina occurs alongside testicular ectopia. There have only been about a hundred and fifty reported cases of TTE; a fifth of these accompanied by PMDS.

PRESENTATION OF CASE

Two middle-aged male patients presented with two separate complaints of inguinoscrotal swellings. In both patients, ultrasonography showed a hernial defect protruding into the scrotum on one side and the testis absent on the contralateral side. During hernia surgery, Mullerian duct remnants were found. Diagnosis of TTE with PMDS was established. Bilateral orchidectomy was done and Mullerian derivatives were excised.

DISCUSSION

There is controversy over the treatment of TTE with PMDS. Some authors,in addition to hernia repair, advocate the preservation of Mullerian structures because of risk to injury to vas deferens while others advocate resection of these structures due to risk of carcinoma. In pediatric patients, orchidopexy should be done to preserve fertility.However, in the older age group, orchidectomy should be done due to an increased risk of testicular carcinoma.

CONCLUSION

TTE should be suspected in cases of unilateral inguinal hernia with contralateral undescended testes. Orchidectomy is recommended in patients older than 12 years old, otherwise, orchidopexy should be done. No Mullerian duct remnants should be left in situ.

摘要

引言

睾丸横过异位(TTE)是一种罕见的情况,即双侧睾丸均降至同一侧,且可位于异位位置。当合并永存苗勒管综合征(PMDS)时,情况更为罕见,此时苗勒管衍生物即输卵管、子宫、宫颈和阴道上三分之二会与睾丸异位并存。据报道,TTE病例仅有约150例;其中五分之一合并PMDS。

病例介绍

两名中年男性患者分别因腹股沟阴囊肿胀前来就诊。在这两名患者中,超声检查均显示一侧有疝缺损突入阴囊,对侧睾丸缺如。在疝修补手术中,发现了苗勒管残余物。确诊为合并PMDS的TTE。进行了双侧睾丸切除术,并切除了苗勒管衍生物。

讨论

对于合并PMDS的TTE的治疗存在争议。一些作者除疝修补外,主张保留苗勒管结构,因为存在损伤输精管的风险;而另一些作者则主张切除这些结构,因为存在癌变风险。对于儿科患者,应进行睾丸固定术以保留生育能力。然而,对于年龄较大的患者,由于睾丸癌风险增加,应进行睾丸切除术。

结论

对于单侧腹股沟疝合并对侧睾丸未降的病例,应怀疑TTE。建议对12岁以上患者进行睾丸切除术,否则应进行睾丸固定术。不应将苗勒管残余物留在原位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcdd/7264951/64d07bd5903b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcdd/7264951/7aff8fc7fcbb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcdd/7264951/64d07bd5903b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcdd/7264951/7aff8fc7fcbb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcdd/7264951/64d07bd5903b/gr2.jpg

相似文献

1
Transverse testicular ectopia with persistent Mullerian duct syndrome: an operative eureka.睾丸横过异位合并苗勒管永存综合征:手术中的重大发现。
Int J Surg Case Rep. 2020;71:338-340. doi: 10.1016/j.ijscr.2020.04.035. Epub 2020 May 11.
2
Lessons learned from five patients of persistent Mullerian duct syndrome: A case series.从五例持续性苗勒管综合征患者身上吸取的经验教训:病例系列
Int J Surg Case Rep. 2022 Aug;97:107459. doi: 10.1016/j.ijscr.2022.107459. Epub 2022 Jul 27.
3
A rare case of male pseudohermaphroditism-persistent mullerian duct syndrome with transverse testicular ectopia - Case report and review of literature.一例罕见的男性假两性畸形——持续性苗勒管综合征合并睾丸横位异位——病例报告及文献复习
Int J Surg Case Rep. 2017;37:72-75. doi: 10.1016/j.ijscr.2017.06.016. Epub 2017 Jun 15.
4
'Testicular masquerade': a case report of testicular malignancy with persistent Müllerian duct syndrome and transverse testicular ectopia.“睾丸伪装综合征”:一例具有持续性 Müller 管发育不全综合征和睾丸横过异位的睾丸恶性肿瘤病例报告。
Ann R Coll Surg Engl. 2024 May;106(5):466-470. doi: 10.1308/rcsann.2023.0088. Epub 2023 Dec 1.
5
Combined persistent Mullerian Duct Syndrome, Transverse Testicular Ectopia and Mosaic Klinefelter's Syndrome.合并持续性苗勒管综合征、睾丸横过异位和嵌合型克兰费尔特综合征。
J Coll Physicians Surg Pak. 2008 Jun;18(6):375-7.
6
Transvers testicular ectopia: A case report and literature review.睾丸横位异位:一例报告及文献综述
Int J Surg Case Rep. 2019;65:361-364. doi: 10.1016/j.ijscr.2019.11.007. Epub 2019 Nov 12.
7
Rare case of transverse testicular ectopia - Case report and review of literature.睾丸横位异位罕见病例——病例报告及文献综述
Int J Surg Case Rep. 2017 Nov 7;41:407-410. doi: 10.1016/j.ijscr.2017.09.032. eCollection 2017.
8
Persistent mullerian duct syndrome: A 24-year experience.持续性苗勒管综合征:24年的经验
J Pediatr Surg. 2016 Oct;51(10):1721-4. doi: 10.1016/j.jpedsurg.2016.06.005. Epub 2016 Jun 13.
9
Persistent mullerian duct syndrome with transverse testicular ectopia: rare entity.持续性苗勒管综合征伴睾丸横位异位:罕见病例。
J Clin Diagn Res. 2014 Mar;8(3):162-3. doi: 10.7860/JCDR/2014/6133.4148. Epub 2014 Mar 15.
10
Persistent Mullerian duct syndrome with transverse testicular ectopia: A case report.持续性苗勒管综合征伴睾丸横位异位:一例报告
Urol Case Rep. 2019 Apr 10;25:100888. doi: 10.1016/j.eucr.2019.100888. eCollection 2019 Jul.

引用本文的文献

1
Fortuitous Persistent Müllerian Duct Syndrome Diagnosis in an Adult Patient With Hematuria: A Case Report.成人血尿患者偶然诊断为持续性苗勒管综合征:一例报告
Clin Case Rep. 2025 Sep 3;13(9):e70836. doi: 10.1002/ccr3.70836. eCollection 2025 Sep.
2
Case Series of Transverse Testicular Ectopia in Children.儿童睾丸横过异位病例系列
J Indian Assoc Pediatr Surg. 2025 Jan-Feb;30(1):76-80. doi: 10.4103/jiaps.jiaps_124_24. Epub 2025 Jan 2.
3
A rare form of male pseudohermaphroditism-Persistent Mullerian Duct Syndrome.一种罕见的男性假两性畸形——持续性苗勒管综合征。

本文引用的文献

1
Persistent Mullerian duct syndrome with transverse testicular ectopia: A case report.持续性苗勒管综合征伴睾丸横位异位:一例报告
Urol Case Rep. 2019 Apr 10;25:100888. doi: 10.1016/j.eucr.2019.100888. eCollection 2019 Jul.
2
Management of Transverse Testicular Ectopia with Persistent Mullerian Duct Syndrome.合并持续性苗勒管综合征的睾丸横过异位的管理
North Clin Istanb. 2018 Aug 8;5(4):357-360. doi: 10.14744/nci.2018.22755. eCollection 2018.
3
The SCARE 2018 statement: Updating consensus Surgical CAse REport (SCARE) guidelines.
J Surg Case Rep. 2022 Dec 30;2022(12):rjac596. doi: 10.1093/jscr/rjac596. eCollection 2022 Dec.
4
Persistent Müllerian Duct Syndrome: Understanding the Challenges.持续性苗勒管综合征:认识挑战
Case Rep Urol. 2022 Mar 27;2022:2643833. doi: 10.1155/2022/2643833. eCollection 2022.
SCARE 2018 声明:更新共识手术病例报告(SCARE)指南。
Int J Surg. 2018 Dec;60:132-136. doi: 10.1016/j.ijsu.2018.10.028. Epub 2018 Oct 18.
4
The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.持续性苗勒管综合征:基于157例个人经验的最新进展
Sex Dev. 2017;11(3):109-125. doi: 10.1159/000475516. Epub 2017 May 20.
5
Laparoscopic hysterectomy with bilateral orchidectomy for Persistent Mullerian duct syndrome with seminoma testes: Case report.腹腔镜子宫切除术联合双侧睾丸切除术治疗持续性苗勒管综合征合并睾丸精原细胞瘤:病例报告
J Minim Access Surg. 2015 Oct-Dec;11(4):273-5. doi: 10.4103/0972-9941.158160.
6
Persistent mullerian duct syndrome with transverse testicular ectopia: rare entity.持续性苗勒管综合征伴睾丸横位异位:罕见病例。
J Clin Diagn Res. 2014 Mar;8(3):162-3. doi: 10.7860/JCDR/2014/6133.4148. Epub 2014 Mar 15.
7
Male form of persistent Mullerian duct syndrome type I (hernia uteri inguinalis) presenting as an obstructed inguinal hernia: a case report.表现为梗阻性腹股沟疝的I型持续性苗勒管综合征男性型(子宫腹股沟疝):一例报告
J Med Case Rep. 2011 Dec 20;5:586. doi: 10.1186/1752-1947-5-586.
8
Transverse testicular ectopia, a case report and review of literature.睾丸横位异位:一例报告并文献复习
Ger Med Sci. 2011;9:Doc15. doi: 10.3205/000138. Epub 2011 Jul 7.
9
Persistent mullerian duct syndrome associated with transverse testicular ectopia.持续性苗勒管综合征伴睾丸横位异位
Ann Saudi Med. 1997 Mar;17(2):226-7. doi: 10.5144/0256-4947.1997.226.