• 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

一例阴茎缺如合并肾发育不全及膀胱直肠瘘的罕见病例报告。

A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula.

作者信息

Kian Behnam, Esmaeilian Saeed, Kayedi Mehrdad

机构信息

Medical Imaging Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

Medical Imaging Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Radiol Case Rep. 2022 Sep 30;17(12):4656-4659. doi: 10.1016/j.radcr.2022.08.107. eCollection 2022 Dec.

DOI:10.1016/j.radcr.2022.08.107
PMID:36204399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9530489/
Abstract

Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder. The incidence of aphallia according to previous studies is about 1 in 10-30 million births. We report a case of a child with the absence of the penis with associated kidney hypoplasia and vesicorectal fistula.

摘要

无阴茎症或阴茎发育不全是泌尿生殖系统的一种罕见病例,与上尿路疾病有关。胚胎期胎儿生殖结节形成失败是该疾病的病因。根据以往研究,无阴茎症的发病率约为每1000万至3000万例出生中有1例。我们报告一例患儿,其阴茎缺如,并伴有肾发育不全和膀胱直肠瘘。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/e3de70c7251b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/a3204d58091c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/c381fbb4bfe9/gr2a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/dcc518d3c5f3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/e3de70c7251b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/a3204d58091c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/c381fbb4bfe9/gr2a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/dcc518d3c5f3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c6/9530489/e3de70c7251b/gr4.jpg

相似文献

1
A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula.一例阴茎缺如合并肾发育不全及膀胱直肠瘘的罕见病例报告。
Radiol Case Rep. 2022 Sep 30;17(12):4656-4659. doi: 10.1016/j.radcr.2022.08.107. eCollection 2022 Dec.
2
A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency.一种新的临床表现:无阴茎、膀胱输尿管反流、直肠膀胱瘘和肾上腺功能不全。
Case Rep Pediatr. 2020 Nov 23;2020:8826520. doi: 10.1155/2020/8826520. eCollection 2020.
3
Aphallia: A Very Rare Congenital Anomaly, With Associated Genitourinary And Ano-Rectal Malformation.无阴茎畸形:一种极为罕见的先天性异常,伴有相关的泌尿生殖系统及肛门直肠畸形。
J Ayub Med Coll Abbottabad. 2018 Apr-Jun;30(2):275-277.
4
Penile Agenesis with Urethrorectal Fistula and Vesicoureteral Reflux.阴茎发育不全伴尿道直肠瘘和膀胱输尿管反流。
Fetal Pediatr Pathol. 2022 Apr;41(2):338-340. doi: 10.1080/15513815.2020.1805533. Epub 2020 Aug 13.
5
A rare case of aphallia with right kidney hypoplasia and left kidney dysplasia.一例罕见的无阴茎畸形合并右肾发育不全及左肾发育异常。
Arch Iran Med. 2015 Apr;18(4):257-9.
6
Male and female aphallia associated with severe urinary tract dysplasia.与严重尿路发育异常相关的男性和女性无阴茎畸形
J Pediatr Urol. 2016 Aug;12(4):268.e1-7. doi: 10.1016/j.jpurol.2016.04.040. Epub 2016 Jun 11.
7
A rare case of penis agenesis (Aphallia) with associated multiple urogenital anomalies.一例罕见的阴茎发育不全(无阴茎畸形)合并多种泌尿生殖系统异常病例。
Int J Surg Case Rep. 2015;15:10-2. doi: 10.1016/j.ijscr.2015.08.004. Epub 2015 Aug 10.
8
A rare presentation: Penile agenesis, vesicoureteral reflux, and rectovesical fistula in a newborn.
Urol Case Rep. 2019 Apr 19;25:100895. doi: 10.1016/j.eucr.2019.100895. eCollection 2019 Jul.
9
Aphallia: A Rare Congenital Anomaly in a Low-Resource Setting.无睾症:资源匮乏地区的一种罕见先天性异常
Int Med Case Rep J. 2023 Aug 23;16:481-484. doi: 10.2147/IMCRJ.S424001. eCollection 2023.
10
[Aphallia - report of two cases].[无睾症——两例报告]
Urologe A. 2020 Jul;59(7):825-828. doi: 10.1007/s00120-020-01244-3.

引用本文的文献

1
A review of literature of a functional, congenital intrathoracic kidney.一篇关于功能性先天性胸内肾的文献综述。
J Cardiothorac Surg. 2025 Jan 5;20(1):20. doi: 10.1186/s13019-024-03306-5.
2
Aphallia - congenital absence of the penis: a systematic review.尿道下裂-先天性阴茎缺失:系统评价。
BMC Urol. 2024 Mar 28;24(1):75. doi: 10.1186/s12894-024-01445-4.

本文引用的文献

1
[Aphallia - report of two cases].[无睾症——两例报告]
Urologe A. 2020 Jul;59(7):825-828. doi: 10.1007/s00120-020-01244-3.
2
A case report of aphallia with urorectal septum malformation sequence in a newborn: a very rarely seen condition.新生儿无阴茎合并尿直肠隔畸形序列征一例报告:一种极为罕见的病症。
Int Med Case Rep J. 2015 Dec 4;8:317-20. doi: 10.2147/IMCRJ.S92122. eCollection 2015.
3
A rare case of aphallia with right kidney hypoplasia and left kidney dysplasia.一例罕见的无阴茎畸形合并右肾发育不全及左肾发育异常。
Arch Iran Med. 2015 Apr;18(4):257-9.
4
Aphallia: a case report and literature review.无睾症:一例病例报告及文献综述。
Afr J Paediatr Surg. 2011 Sep-Dec;8(3):324-5. doi: 10.4103/0189-6725.91675.
5
Male gender assignment in aphallia: a case report and review of the literature.
Int Urol Nephrol. 2005;37(2):317-9. doi: 10.1007/s11255-004-7974-0.
6
Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate. Case report.一名存活男婴阴茎、膀胱及尿道缺如合并肛门直肠畸形。病例报告。
Clin Exp Obstet Gynecol. 1999;26(3-4):225-6.
7
Diagnosis and current management of penile agenesis.阴茎发育不全的诊断与当前治疗
J Pediatr Surg. 1998 Apr;33(4):628-31. doi: 10.1016/s0022-3468(98)90330-x.
8
Aphallia: its classification and management.无睾症:其分类与处理
J Urol. 1989 Mar;141(3):589-92. doi: 10.1016/s0022-5347(17)40903-7.