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原发性先天性膀胱憩室:输尿管引流至何处?

Primary congenital bladder diverticula: Where does the ureter drain?

作者信息

Macedo Antonio, Garrone Gilmar, Ottoni Sérgio Leite, Oliveira Diego Estevam, Souza Geórgia Rubiane Meira do Rosário, Cruz Marcela Leal da

机构信息

Department of Pediatrics, Federal University of São Paulo, São Paulo, Brazil.

出版信息

Afr J Paediatr Surg. 2015 Oct-Dec;12(4):280-5. doi: 10.4103/0189-6725.172574.

Abstract

BACKGROUND

Primary congenital bladder diverticulum (PCBD) is related to a deficient detrusor layer allowing out-pouching of the bladder mucosa through the inadequate muscularis wall. We aimed to review our experience with symptomatic PCBD in order to correlate clinical findings with anatomical aspects and to present late outcome.

MATERIALS AND METHODS

We reviewed all patients operated in our institution since 2004. We evaluated the charts for complaints, radiological exams, method of treatment, complications and length of follow-up.

RESULTS

We treated 10 cases (11 renal units - [RU]), predominantly males (9/10), mean age at surgery of 5.3 years. All patients had significant urological complaints presenting either with antenatal hydronephrosis (4) or febrile urinary tract infection (5) and urinary retention in one. The ureter was found implanted inside the diverticulum in 8/11 RU. An extravesical psoas-hitch ureteroneocystostomy and diverticulum resection was performed in 10/11 cases, whereas 1 case was treated intravesically based on surgeon's preference without performing cystoscopy. Mean follow-up was 34.1 months (1-120) without complications.

CONCLUSIONS

PCBD is an uncommon diagnosis and has a high probability of drainage inside the diverticulum (72.7%). We recommend the extravesical approach associated with diverticulectomy and ureteroneocystostomy as the preferred technique to treat this abnormality.

摘要

背景

原发性先天性膀胱憩室(PCBD)与逼尿肌层缺陷有关,致使膀胱黏膜通过肌层壁薄弱处向外膨出。我们旨在回顾我们对有症状PCBD的治疗经验,以便将临床发现与解剖学特征相关联,并展示远期结果。

材料与方法

我们回顾了自2004年以来在我院接受手术的所有患者。我们评估了病历中的症状、影像学检查、治疗方法、并发症及随访时间。

结果

我们共治疗了10例患者(11个肾单位 - [RU]),以男性为主(9/10),手术时的平均年龄为5.3岁。所有患者均有明显的泌尿系统症状,表现为产前肾积水(4例)或发热性尿路感染(5例),1例有尿潴留。在11个肾单位中的8个中发现输尿管植入憩室内。11例中有10例进行了膀胱外腰大肌悬吊输尿管膀胱吻合术及憩室切除术,而1例根据外科医生的偏好采用膀胱内治疗,未进行膀胱镜检查。平均随访时间为34.1个月(1 - 120个月),无并发症发生。

结论

PCBD是一种罕见的诊断,憩室内引流的可能性很高(72.7%)。我们建议将膀胱外途径联合憩室切除术及输尿管膀胱吻合术作为治疗这种异常情况的首选技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb4/4955463/bb17827cbcd3/AJPS-12-280-g001.jpg

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