• 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

梨状腹综合征的发病机制。

Pathogenesis of the prune belly syndrome.

作者信息

Stephens F D, Gupta D

机构信息

Royal Children's Hospital, Melbourne, Australia.

出版信息

J Urol. 1994 Dec;152(6 Pt 2):2328-31. doi: 10.1016/s0022-5347(17)31669-5.

DOI:10.1016/s0022-5347(17)31669-5
PMID:7966734
Abstract

The triad of abnormalities of the prune belly syndrome may arise simply from the effects of early urethral obstruction or alternatively from a basic defect of the mesoderm from which the triad of abnormalities develops. The urethra and genital tract of 21 prune belly syndrome specimens and 23 specimens of Young's posterior urethral valves types 1 and 3 were compared in a study for differences in the pathological anatomy that may elucidate the controversy. The specimens were dissected and investigated radiographically and histologically. The seminal ducts and vesicles, and prostatic glands were abnormal in the prune belly syndrome specimens and normally developed in the posterior urethral valve specimens. We contest that this major difference stems from a primary defect of the intermediate and lateral plate mesoderm in the prune belly syndrome which would affect the embryogenesis not only of the mesonephric and paramesonephric ducts but also of the musculature of the abdominal wall and urinary organs, and that prune belly valves when present are intrinsic components of the mesodermal defect of the prune belly syndrome urethra.

摘要

梅干腹综合征的三联征异常可能仅仅源于早期尿道梗阻的影响,或者源于中胚层的基本缺陷,三联征异常由此发展而来。在一项旨在阐明争议的研究中,对21例梅干腹综合征标本以及23例1型和3型杨氏后尿道瓣膜标本的尿道和生殖道进行了比较,以研究可能存在的病理解剖差异。对标本进行了解剖,并进行了放射学和组织学检查。梅干腹综合征标本中的输精管、精囊和前列腺异常,而后尿道瓣膜标本中的这些结构发育正常。我们认为,这一主要差异源于梅干腹综合征中侧板和侧板中胚层的原发性缺陷,这不仅会影响中肾管和副中肾管的胚胎发育,还会影响腹壁和泌尿器官的肌肉组织,并且梅干腹瓣膜(若存在)是梅干腹综合征尿道中胚层缺陷的固有组成部分。

相似文献

1
Pathogenesis of the prune belly syndrome.梨状腹综合征的发病机制。
J Urol. 1994 Dec;152(6 Pt 2):2328-31. doi: 10.1016/s0022-5347(17)31669-5.
2
Testicular histology in fetuses with the prune belly syndrome and posterior urethral valves.患有梅干腹综合征和后尿道瓣膜症的胎儿的睾丸组织学
J Urol. 1988 Feb;139(2):335-7. doi: 10.1016/s0022-5347(17)42403-7.
3
Fetal bladder histology in posterior urethral valves and the prune belly syndrome.后尿道瓣膜症及梅干腹综合征中的胎儿膀胱组织学
J Urol. 1990 Aug;144(2 Pt 1):337-9. doi: 10.1016/s0022-5347(17)39448-x.
4
Etiology of prune belly syndrome: evidence of megalocystic origin in an early fetus.梅干腹综合征的病因:早期胎儿巨膀胱起源的证据。
Obstet Gynecol. 1994 May;83(5 Pt 2):865-8.
5
Prune belly syndrome in females: a triad of abdominal musculature deficiency and anomalies of the urinary and genital systems.女性梅干腹综合征:一种由腹部肌肉组织缺陷以及泌尿系统和生殖系统异常组成的三联征。
J Pediatr. 1991 Mar;118(3):395-8. doi: 10.1016/s0022-3476(05)82153-5.
6
Prostate development in prune belly syndrome (PBS) and posterior urethral valves (PUV): etiology of PBS--lower urinary tract obstruction or primary mesenchymal defect?梅干腹综合征(PBS)和后尿道瓣膜(PUV)中的前列腺发育:PBS的病因——下尿路梗阻还是原发性间充质缺陷?
Pediatr Pathol. 1991 Jan-Feb;11(1):1-29. doi: 10.3109/15513819109064739.
7
Patterns of congenital lower urinary tract obstructive uropathy: relation to abnormal prostate and bladder development and the prune belly syndrome.先天性下尿路梗阻性肾病的模式:与前列腺和膀胱发育异常及梅干腹综合征的关系。
Pediatr Dev Pathol. 2001 Sep-Oct;4(5):467-72. doi: 10.1007/s10024001-0042-1.
8
Urethral and genital malformations in prune belly syndrome.梅干腹综合征中的尿道和生殖器畸形
J Urol. 1982 Jan;127(1):94-6. doi: 10.1016/s0022-5347(17)53624-1.
9
Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasia.梨状腹综合征的发病机制:前列腺发育不全导致的功能性尿道梗阻。
Pediatrics. 1984 Apr;73(4):470-5.
10
Bladder distention and pyelectasis in the male fetus: causes, comparisons, and contrasts.男性胎儿的膀胱扩张和肾盂积水:病因、比较与对比。
J Ultrasound Med. 1998 Dec;17(12):743-9. doi: 10.7863/jum.1998.17.12.743.

引用本文的文献

1
Prune belly syndrome: A rare case report.梅干腹综合征:一例罕见病例报告。
Clin Case Rep. 2024 Jun 17;12(6):e8922. doi: 10.1002/ccr3.8922. eCollection 2024 Jun.
2
Dental treatment of patients with prune belly syndrome.梅干腹综合征患者的牙科治疗。
Spec Care Dentist. 2023 Jan;43(1):67-72. doi: 10.1111/scd.12728. Epub 2022 May 8.
3
Case Report: Novel Copy Number Variant 16p11.2 Duplication Associated With Prune Belly Syndrome.病例报告:与梅干腹综合征相关的新型16p11.2拷贝数变异重复
Front Pediatr. 2021 Sep 23;9:729932. doi: 10.3389/fped.2021.729932. eCollection 2021.
4
Modern management of and update on prune belly syndrome.普拉泽-威利综合征的现代管理与更新。
J Pediatr Urol. 2021 Aug;17(4):548-554. doi: 10.1016/j.jpurol.2021.04.010. Epub 2021 Apr 24.
5
The role of intra-abdominal pressure in human testicular migration.腹腔内压力在人类睾丸迁移中的作用。
Int Braz J Urol. 2021 Jan-Feb;47(1):36-44. doi: 10.1590/S1677-5538.IBJU.2021.99.03.
6
Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene.男性存活的梅干腹综合征可能是由 X 连锁细丝蛋白 A 基因的杂合错义突变引起的。
BMC Med Genet. 2020 Feb 21;21(1):38. doi: 10.1186/s12881-020-0973-x.
7
Unusual presentation of prune belly syndrome: a case report.梅干腹综合征的罕见表现:一例病例报告
J Med Case Rep. 2017 Dec 4;11(1):337. doi: 10.1186/s13256-017-1487-9.
8
Rare copy number variants identified in prune belly syndrome.在梅干腹综合征中鉴定出的罕见拷贝数变异。
Eur J Med Genet. 2018 Mar;61(3):145-151. doi: 10.1016/j.ejmg.2017.11.008. Epub 2017 Nov 23.
9
Outcomes of renal replacement therapy in boys with prune belly syndrome: findings from the ESPN/ERA-EDTA Registry.男性先天性腹壁肌肉发育不良综合征行肾脏替代治疗的结局:来自 ESPN/ERA-EDTA 登记处的研究结果。
Pediatr Nephrol. 2018 Jan;33(1):117-124. doi: 10.1007/s00467-017-3770-9. Epub 2017 Aug 4.
10
Prune-belly syndrome: an autopsy case report.梅干腹综合征:一例尸检病例报告。
Autops Case Rep. 2014 Mar 30;4(4):35-41. doi: 10.4322/acr.2014.037. eCollection 2014 Oct-Dec.