• 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

一名患有克-特综合征成年男性阴茎勃起时出现无痛性尿道出血:病例报告

Painless Urethral Bleeding During Penile Erection in an Adult Man With Klippel-Trenaunay Syndrome: A Case Report.

作者信息

Lei Hongen, Guan Xing, Han Hu, Qian Xiaosong, Zhou Xiaoguang, Zhang Xiaodong, Tian Long

机构信息

Department of Urology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Department of Urology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

出版信息

Sex Med. 2018 Jun;6(2):180-183. doi: 10.1016/j.esxm.2017.12.001. Epub 2018 Feb 13.

DOI:10.1016/j.esxm.2017.12.001
PMID:29452831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5960021/
Abstract

INTRODUCTION

Klippel-Trenaunay syndrome (KTS) is a rare congenital vascular disorder characterized by a triad of cutaneous port wine capillary malformations, varicose veins, and hemihypertrophy of bone and soft tissues.

AIMS

To report on a rare case of KTS in an adult man manifested by painless urethral bleeding during penile erection briefly review the clinical presentation and management of the genitourinary forms of this syndrome.

METHODS

On presentation, the clinical features of this patient, including medical history, signs and symptoms, and imaging examinations, were recorded. After diagnosis and initial treatment, a literature review of the urethral features of KTS was performed and is discussed in this report.

RESULTS

A 35-year-old man with KTS presented with painless urethral bleeding during penile erection that was associated with posterior urethral vascular malformations. The coagulation method was used to treat the malformation, and no urethral bleeding or gross hematuria occurred during a postoperative follow-up period of 6 months.

CONCLUSION

This case demonstrates that coagulation therapy and careful follow-up can be adequate treatment approaches for urethral features of KTS. However, the long-term efficacy of coagulation for this disorder should be investigated further. Lei H, Guan X, Han H, et al. Painless Urethral Bleeding During Penile Erection in an Adult Man With Klippel-Trenaunay Syndrome: A Case Report. Sex Med 2018;6:180-183.

摘要

引言

克-特综合征(KTS)是一种罕见的先天性血管疾病,其特征为皮肤葡萄酒色斑状毛细血管畸形、静脉曲张以及骨骼和软组织半侧肥大三联征。

目的

报告一例成年男性克-特综合征罕见病例,其表现为阴茎勃起时无痛性尿道出血,并简要回顾该综合征泌尿生殖系统表现的临床特征及治疗方法。

方法

记录该患者的临床表现,包括病史、体征和症状以及影像学检查结果。在诊断和初步治疗后,对克-特综合征的尿道特征进行文献回顾并在本报告中进行讨论。

结果

一名35岁克-特综合征男性患者出现阴茎勃起时无痛性尿道出血,这与后尿道血管畸形有关。采用凝固法治疗该畸形,术后6个月随访期间未出现尿道出血或肉眼血尿。

结论

该病例表明,凝固疗法和仔细随访可能是治疗克-特综合征尿道表现的适当方法。然而,凝固疗法对该疾病的长期疗效仍需进一步研究。雷H,关X,韩H等。成年男性克-特综合征患者阴茎勃起时无痛性尿道出血:一例报告。性医学2018;6:180 - 183。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dcd/5960021/6106d0450dfb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dcd/5960021/6106d0450dfb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dcd/5960021/6106d0450dfb/gr1.jpg

相似文献

1
Painless Urethral Bleeding During Penile Erection in an Adult Man With Klippel-Trenaunay Syndrome: A Case Report.一名患有克-特综合征成年男性阴茎勃起时出现无痛性尿道出血:病例报告
Sex Med. 2018 Jun;6(2):180-183. doi: 10.1016/j.esxm.2017.12.001. Epub 2018 Feb 13.
2
A mild and rare form of Klippel-Trenaunay syndrome presenting with urethral bleeding due to penile hemangioma.一种轻度且罕见的 Klippel-Trenaunay 综合征,表现为阴茎血管瘤导致的尿道出血。
Urology. 2011 Feb;77(2):463-5. doi: 10.1016/j.urology.2010.05.018. Epub 2010 Aug 16.
3
Penile prosthesis implant for primary erectile dysfunction in patient with Klippel-Trenaunay syndrome complicated by consumptive coagulopathy: A case report.阴茎假体植入治疗合并消耗性凝血病的克-特综合征患者原发性勃起功能障碍:一例报告
Medicine (Baltimore). 2019 Aug;98(32):e16741. doi: 10.1097/MD.0000000000016741.
4
Uterine Involvement in Klippel-Trenaunay Syndrome: A Rare But Relevant Event. Review of the Literature.子宫受累于克-特综合征:一种罕见但相关的情况。文献综述
Front Surg. 2022 May 12;9:893320. doi: 10.3389/fsurg.2022.893320. eCollection 2022.
5
Recurrent hematuria involving urinary system with Klippel-Trenaunay syndrome: A case report.Klippel-Trenaunay 综合征累及泌尿系统的复发性血尿:病例报告。
Medicine (Baltimore). 2024 Feb 16;103(7):e36923. doi: 10.1097/MD.0000000000036923.
6
Easily misdiagnosed complex Klippel-Trenaunay syndrome: A case report.易误诊的复杂型克-特综合征:一例报告
World J Clin Cases. 2023 Feb 6;11(4):922-930. doi: 10.12998/wjcc.v11.i4.922.
7
Case Report: Klippel-Trenaunay Syndrome - Recurrent Venous Thromboembolism and Vascular Malformation.病例报告:克-特综合征——复发性静脉血栓栓塞与血管畸形
Int Med Case Rep J. 2020 May 21;13:195-200. doi: 10.2147/IMCRJ.S236027. eCollection 2020.
8
Lower gastrointestinal bleeding, hematuria and splenic hemangiomas in Klippel-Trenaunay syndrome: a case report and literature review.Klippel-Trenaunay综合征中的下消化道出血、血尿和脾血管瘤:一例报告及文献综述
Turk J Gastroenterol. 2009 Mar;20(1):62-6.
9
Klippel Trenaunay syndrome in a 3-year-old: A case report.一名3岁儿童的克-特综合征:病例报告
Int J Surg Case Rep. 2022 Oct;99:107673. doi: 10.1016/j.ijscr.2022.107673. Epub 2022 Sep 17.
10
Subcutaneous Cavernous Haemangioma in a Patient with Klippel-Trenaunay Syndrome: A Case Report.患者患有 Klippel-Trenaunay 综合征,伴发皮下海绵状血管瘤:病例报告。
Curr Med Imaging. 2024;20:e15734056251193. doi: 10.2174/0115734056251193231016042812.

引用本文的文献

1
Clinical characteristics and endoscopic treatment of hematospermia with postcoital hematuria.血精伴性交后血尿的临床特征和内镜治疗。
BMC Urol. 2020 Jun 29;20(1):78. doi: 10.1186/s12894-020-00646-x.
2
Embolization with microcoils for urethral hemorrhage: A case report.微线圈栓塞治疗尿道出血:一例报告。
Medicine (Baltimore). 2019 Jul;98(27):e16184. doi: 10.1097/MD.0000000000016184.
3
Multiple Urethral Hemangiomas Associated with Urethral Stricture: An Uncommon Aetiology for Urethral Bleeding.多发性尿道血管瘤伴尿道狭窄:一种罕见的尿道出血病因

本文引用的文献

1
Diagnosis and management of the venous malformations of Klippel-Trénaunay syndrome.克莱伯-特雷纳综合征静脉畸形的诊断与治疗。
J Vasc Surg Venous Lymphat Disord. 2017 Jul;5(4):587-595. doi: 10.1016/j.jvsv.2016.10.084.
2
An Unusual Etiology for Hematospermia and Treatments That Were Successful.血精症的一种罕见病因及成功的治疗方法。
Urology. 2015 Oct;86(4):740-3. doi: 10.1016/j.urology.2015.06.031. Epub 2015 Jul 16.
3
Dominant inheritance and intra-familial variations in the association of Sturge-Weber and Klippel-Trenaunay-Weber syndromes.
Case Rep Urol. 2019 Feb 3;2019:9071327. doi: 10.1155/2019/9071327. eCollection 2019.
斯特奇-韦伯综合征与克-特-韦综合征关联中的显性遗传及家族内变异
Indian J Hum Genet. 2010 Jan;16(1):26-7. doi: 10.4103/0971-6866.64943.
4
A mild and rare form of Klippel-Trenaunay syndrome presenting with urethral bleeding due to penile hemangioma.一种轻度且罕见的 Klippel-Trenaunay 综合征,表现为阴茎血管瘤导致的尿道出血。
Urology. 2011 Feb;77(2):463-5. doi: 10.1016/j.urology.2010.05.018. Epub 2010 Aug 16.
5
Lower gastrointestinal bleeding, hematuria and splenic hemangiomas in Klippel-Trenaunay syndrome: a case report and literature review.Klippel-Trenaunay综合征中的下消化道出血、血尿和脾血管瘤:一例报告及文献综述
Turk J Gastroenterol. 2009 Mar;20(1):62-6.
6
Klippel-Trenaunay syndrome: diagnostic criteria and hypothesis on etiology.克-特综合征:诊断标准及病因假说
Ann Plast Surg. 2008 Feb;60(2):217-23. doi: 10.1097/SAP.0b013e318062abc1.
7
Klippel-Trenaunay syndrome: incidence and treatment of genitourinary sequelae.克-特综合征:泌尿生殖系统后遗症的发病率及治疗
J Urol. 2007 Apr;177(4):1244-9. doi: 10.1016/j.juro.2006.11.099.
8
Inverse Klippel-Trenaunay syndrome: review of cases showing deficient growth.反向克-特综合征:生长发育不足病例回顾
Dermatology. 2007;214(2):130-2. doi: 10.1159/000098571.
9
Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth.克-特综合征:一种多系统疾病,可能由导致血管和组织过度生长的致病基因引起。
Int J Dermatol. 2006 Aug;45(8):883-90. doi: 10.1111/j.1365-4632.2006.02940.x.
10
Life-threatening gross hematuria due to genitourinary manifestation of Klippel-Trenaunay syndrome.因克-特综合征的泌尿生殖系统表现导致的危及生命的严重血尿。
Int Urol Nephrol. 2006;38(1):137-40. doi: 10.1007/s11255-005-3154-0.