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1
Bladder agenesis and incomplete kidney duplication: Ileal reservoir with continent diversion as definitive treatment.膀胱发育不全与不完全性肾重复畸形：以可控性回肠膀胱术作为确定性治疗方法。
Can Urol Assoc J. 2015 Mar-Apr;9(3-4):E142-4. doi: 10.5489/cuaj.2534.
2
Urethral duplication with single bladder and multiple genitourinary abnormalities: an example of continent urinary diversion.伴有单一膀胱及多种泌尿生殖系统异常的重复尿道：可控性尿流改道的一个实例。
J Pediatr Surg. 1990 Dec;25(12):1285-6. doi: 10.1016/0022-3468(90)90534-g.
3
Urinary diversion via a continent ileal reservoir: clinical results in 12 patients.通过可控回肠膀胱术进行尿流改道：12例患者的临床结果
J Urol. 1982 Sep;128(3):469-75. doi: 10.1016/s0022-5347(17)53001-3.
4
Urinary diversion and orthotopic bladder substitution in children and young adults with neurogenic bladder: a safe option for treatment?儿童和年轻成人神经源性膀胱的尿流改道和原位膀胱替代：一种安全的治疗选择？
J Urol. 2000 Feb;163(2):568-73.
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[Indiana continent urinary reservoir: report of 15 cases].[印第安纳洲可控性膀胱术：15例报告]
Hinyokika Kiyo. 1989 May;35(5):795-805.
6
Bladder neck closure in children: a decade of followup.儿童膀胱颈闭合术：十年随访
J Urol. 2009 Oct;182(4 Suppl):1797-801. doi: 10.1016/j.juro.2009.03.074. Epub 2009 Aug 18.
7
[Multiple stones in atypical heterotopic reservoir in a patient with renal transplant: endourologic resolution].[肾移植患者非典型异位储尿囊内多发结石：腔内泌尿外科解决方案]
Urologia. 2011 Oct;78 Suppl 18:49-53. doi: 10.5301/RU.2011.8775.
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[Continent urinary diversion: the Mitrofanoff principle].[可控性尿流改道：米氏原理]
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Orthotopic lower urinary tract reconstruction in women using the Kock ileal neobladder: updated experience in 34 patients.采用科克回肠新膀胱对女性进行原位下尿路重建：34例患者的最新经验
J Urol. 1997 Aug;158(2):400-5.
10
Experience with the ileal bladder (Camey procedure) and cecoileal reservoirs for continent urinary diversion.回肠膀胱术（卡米手术）及盲肠回肠储尿囊用于可控性尿流改道的经验。
Semin Urol. 1987 Feb;5(1):28-45.

引用本文的文献

1
Congenital anomalies of the kidney and urinary tract.肾脏和泌尿系统先天性异常。
Front Med (Lausanne). 2024 Jul 15;11:1384676. doi: 10.3389/fmed.2024.1384676. eCollection 2024.
2
Bladder Agenesis: A Systematic Review.膀胱发育不全：一项系统综述。
Cureus. 2023 Sep 12;15(9):e45121. doi: 10.7759/cureus.45121. eCollection 2023 Sep.
3
A case of urinary bladder agenesis and bilateral ectopic ureters: a case report.膀胱缺如及双侧异位输尿管一例：病例报告
BMC Urol. 2018 Sep 26;18(1):83. doi: 10.1186/s12894-018-0396-6.
4
Bladder agenesis, ectopic ureters and a multicystic dysplastic horseshoe kidney in one twin newborn with normal amniotic fluid index in utero.一名双胎新生儿膀胱发育不全、输尿管异位及多囊性发育不良马蹄肾，宫内羊水指数正常。
BMJ Case Rep. 2016 Dec 8;2016:bcr2016216518. doi: 10.1136/bcr-2016-216518.

本文引用的文献

1
Bilateral ectopic ureters with bladder agenesis.双侧异位输尿管伴膀胱发育不全。
J Pak Med Assoc. 2012 Oct;62(10):1086-9.
2
A continent urinary diversion in a female with agenesis of the bladder: a 5-year follow-up.女性膀胱发育不全行 continent 式尿流改道术：5 年随访。
Urology. 2012 Aug;80(2):437-9. doi: 10.1016/j.urology.2011.12.010. Epub 2012 Feb 18.
3
Triad of bladder agenesis with solitary kidney and ectopic ureter.膀胱发育不全合并孤立肾及异位输尿管三联征。
Indian J Urol. 2008 Oct;24(4):566-8. doi: 10.4103/0970-1591.44271.
4
Bladder agenesis in a male neonate.
J Pediatr Surg. 2008 Nov;43(11):e1-3. doi: 10.1016/j.jpedsurg.2008.06.003.
5
Single system ectopic ureter to rectum subtending solitary kidney and bladder agenesis in newborn male.新生儿男性单系统异位输尿管至直肠伴孤立肾和膀胱缺如
Urology. 2006 Dec;68(6):1344.e1-3. doi: 10.1016/j.urology.2006.09.048.
6
Agenesis of the bladder.
J Am Med Assoc. 1959 Apr 25;169(17):2016-8. doi: 10.1001/jama.1959.73000340001013.
7
A case of bladder agenesis.一例膀胱发育不全病例。
Australas Radiol. 1997 May;41(2):201-3. doi: 10.1111/j.1440-1673.1997.tb00717.x.
8
Agenesis of bladder.膀胱发育不全
J Urol. 1972 Apr;107(4):660-1. doi: 10.1016/s0022-5347(17)61107-8.

膀胱发育不全与不完全性肾重复畸形：以可控性回肠膀胱术作为确定性治疗方法。

Bladder agenesis and incomplete kidney duplication: Ileal reservoir with continent diversion as definitive treatment.

作者信息

Pacheco-Mendoza Byron Alexis, González-Ledón Fernando J, Díaz-Pardo Mario, Soto-Blanquel Juan L, Castelán-Martínez Osvaldo Daniel

机构信息

Urology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico;

Clinical Epidemiology Unit, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.

出版信息

Can Urol Assoc J. 2015 Mar-Apr;9(3-4):E142-4. doi: 10.5489/cuaj.2534.

DOI:10.5489/cuaj.2534
PMID:25844102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4375002/
Abstract

Bladder agenesis is an extremely rare entity. A 12-year-old female patient presented with urinary incontinence, recurrent urinary tract infections, visible vaginal introitus and urethra, and two holes at the vulvar vestibule. An investigation revealed bladder agenesis. Surgery confirmed the absence of bladder, and ileal reservoir in omega (Ω) was performed with continent diversion. At the 30-month follow-up, there was no complication in clean intermittent catheterization.

摘要

膀胱发育不全是一种极其罕见的病症。一名12岁女性患者出现尿失禁、反复尿路感染、可见阴道开口和尿道，以及外阴前庭有两个孔。一项检查显示为膀胱发育不全。手术证实膀胱缺失，并进行了Ω形回肠储尿囊及可控性尿流改道术。在30个月的随访中，清洁间歇性导尿未出现并发症。