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膀胱重复畸形 - 病例系列

Bladder Duplication - A Case Series.

机构信息

University of Colorado School of Medicine, Aurora, CO.

Department of Visceral and Thoracic Surgery, Cantonal Hospital of Winterthur, Switzerland.

出版信息

Urology. 2021 Mar;149:199-205. doi: 10.1016/j.urology.2020.11.001. Epub 2020 Nov 13.

DOI:10.1016/j.urology.2020.11.001
PMID:33189736
Abstract

OBJECTIVE

To describe 5 cases with complete urinary bladder duplication, their associated conditions, and their respective treatment. Urinary bladder duplication is an extremely rare congenital anomaly of the urinary system. So far about 70 cases have been published in the English literature, most of them as case reports and a few case series.

METHODS AND RESULTS

All consecutive patients with bladder duplication treated at our institution between 2000 and 2015 were included. Patient records were retrospectively analyzed, and 5 patients with urinary bladder duplication were identified (see Summary Figure). Two patients were male. All duplications were recognized by health care providers. In 1 case recognition was prenatal (MRI in utero at 22 weeks of gestation), the latest recognition was at 12 months of age. A voiding cystourethrography was performed in 4 patients to confirm the diagnosis. In 4 patients the bladder duplication could be classified according to Abrahamson with 3 complete reduplications and one complete sagittal septum. All patients suffered from associated congenital diseases, but only one patient had urinary tract infections. Surgical treatment was only performed in one patient. Median follow-up was 34 months.

DISCUSSION

Urinary bladder duplications reflect extremely seldom disorders that are almost always associated with other congenital anomalies. Treatment depends on patients' symptoms and associated conditions and hence needs to be individualized to each patient.

摘要

目的

描述 5 例完全性膀胱重复畸形患者的相关情况及其治疗方法。膀胱重复畸形是一种极其罕见的泌尿系统先天性畸形。目前,在英文文献中已报道约 70 例,其中大多数为病例报告,少数为病例系列。

方法和结果

本研究纳入了 2000 年至 2015 年在我院治疗的所有连续的膀胱重复畸形患者。回顾性分析患者病历,共发现 5 例膀胱重复畸形患者(见概要图)。其中 2 例为男性。所有的重复畸形均由医护人员发现。1 例在产前(妊娠 22 周时的 MRI)发现,最晚的发现时间为 12 个月。4 例患者行排尿性膀胱尿道造影以明确诊断。根据 Abrahamson 的分类,4 例患者的膀胱重复畸形可分为 3 例完全性重复和 1 例完全性矢状隔。所有患者均患有其他先天性疾病,但仅 1 例患者发生过尿路感染。仅 1 例患者接受了手术治疗。中位随访时间为 34 个月。

讨论

膀胱重复畸形是罕见的疾病,几乎总是与其他先天性畸形有关。治疗取决于患者的症状和合并症,因此需要个体化治疗。

相似文献

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Bladder Duplication - A Case Series.膀胱重复畸形 - 病例系列
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Urethral duplication--a wide spectrum of anomalies.尿道重复畸形——一种广泛的异常。
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引用本文的文献

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Front Urol. 2023 Feb 21;3:1080410. doi: 10.3389/fruro.2023.1080410. eCollection 2023.
2
Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report.膀胱不完全重复畸形的迟发性表现:一例意外误诊的罕见病例报告
Urol Case Rep. 2025 May 19;61:103074. doi: 10.1016/j.eucr.2025.103074. eCollection 2025 Jul.
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Bladder duplication in the male cat: the first case report in China.
公猫膀胱重复畸形:中国首例报告。
BMC Vet Res. 2024 Sep 6;20(1):397. doi: 10.1186/s12917-024-04178-6.
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Bladder duplication in a patient with a persistent urogenital sinus: Case report and systematic review of the literature.一名患有持续性泌尿生殖窦患者的膀胱重复畸形:病例报告及文献系统综述
Urol Case Rep. 2024 Apr 10;54:102736. doi: 10.1016/j.eucr.2024.102736. eCollection 2024 May.
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Pre- and postnatal findings with rare congenital anomalies of urinary bladder.膀胱罕见先天性异常的产前和产后检查结果
Clin Case Rep. 2024 Mar 29;12(4):e8590. doi: 10.1002/ccr3.8590. eCollection 2024 Apr.
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Sagittal septum duplication of bladder and duplication of posterior urethra combined with congenital megacolon: a case report and literature review.膀胱矢状隔重复和后尿道重复合并先天性巨结肠:一例病例报告及文献复习。
BMC Urol. 2024 Jan 3;24(1):9. doi: 10.1186/s12894-023-01395-3.
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A Triplicated Bladder with Diphallia; Rare Variant of Duplicate Exstrophy.合并双阴茎的重复膀胱;重复膀胱外翻的罕见变异型
Res Rep Urol. 2023 Mar 3;15:109-112. doi: 10.2147/RRU.S397296. eCollection 2023.
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Bladder duplication in infant girls: role of imaging in two rare cases with variants of a complete sagittal septum.婴儿女孩的膀胱重复畸形:两种罕见病例中完全矢状隔变异的影像学作用。
Pediatr Radiol. 2023 May;53(5):1033-1038. doi: 10.1007/s00247-023-05603-y. Epub 2023 Jan 23.
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Incomplete sagittal septum of the bladder with cystolithiasis.膀胱矢状隔不完整伴膀胱结石
IJU Case Rep. 2022 Apr 30;5(4):264-267. doi: 10.1002/iju5.12451. eCollection 2022 Jul.