Suppr超能文献

尿道重复畸形——19例病例系列的流行病学、诊断与治疗

Urethral duplication-Epidemiology, diagnosis, and treatment in a case series of 19 patients.

作者信息

Guglielmetti Laura Chiara, Delcont Mellissa, Walker Jonathan, Wilcox Duncan, Vuille-Dit-Bille Raphael N

机构信息

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

University of Colorado School of Medicine, Anschutz Medical Campus, Colorado, USA.

出版信息

J Pediatr Urol. 2020 Jun;16(3):385.e1-385.e9. doi: 10.1016/j.jpurol.2020.02.010. Epub 2020 Feb 24.

Abstract

BACKGROUND

Urethral duplications are rare congenital anomalies of the urinary tract. Because of their rare occurrence, evidence about epidemiology, diagnosis and treatment is limited.

OBJECTIVE

The aim of this study was to describe the characteristics, presentation, and treatment of a single large cohort of patients.

STUDY DESIGN

The authors describe a cohort of 19 consecutive patients with urethral duplications treated at a single referral institution over a 15-year period. Type of duplication, comorbidities, diagnosis, and treatments are described.

RESULTS

68% of the patients were male, and the age at diagnosis ranged from 0 days to 120 months. The most common type of urethral duplication in this cohort of patients was IIA-2 according to Effmann (26%). Diagnosis was made by healthcare providers in 90% and by the children's mothers in 10% of the patients. Furthermore, 10% of patients presented with urinary tract infections. Only 26% of the patients did not have associated diseases or disorders. Fifteen (79%) patients were treated surgically, with a mean number of 2 (standard deviation 1.6) surgeries per patient. Surgeries were performed ranging between 2 days and 10 years of age.

DISCUSSION

The authors report one of the largest cohorts of patients with urethral duplication. There was a male preponderance, urinary tract infections were rare, and most patients had associated disorders, which is in line with previous reports. In this cohort, most duplications were discovered by healthcare providers, and a small number of patients did not undergo surgical treatment. The broad spectrum of duplications could be confirmed with type IIA-2 being the most common type. The mean number of two procedures per patient was low compared with previous reports.

摘要

背景

尿道重复畸形是一种罕见的先天性泌尿系统异常。由于其发病率低,关于流行病学、诊断和治疗的证据有限。

目的

本研究旨在描述一大组患者的特征、临床表现及治疗情况。

研究设计

作者描述了在一家转诊机构15年间连续治疗的19例尿道重复畸形患者的队列。描述了重复畸形的类型、合并症、诊断及治疗情况。

结果

68%的患者为男性,诊断年龄从0天至120个月不等。根据埃夫曼分类,该队列中最常见的尿道重复畸形类型为IIA-2型(26%)。90%的患者由医疗保健人员诊断,10%由患儿母亲诊断。此外,10%的患者出现尿路感染。仅26%的患者无相关疾病或病症。15例(79%)患者接受了手术治疗,每位患者平均手术次数为2次(标准差1.6)。手术在患者2天至10岁之间进行。

讨论

作者报告了最大的尿道重复畸形患者队列之一。男性占多数,尿路感染罕见,且大多数患者有相关病症,这与先前的报告一致。在该队列中,大多数重复畸形由医疗保健人员发现,少数患者未接受手术治疗。可以确认重复畸形类型广泛,其中IIA-2型最为常见。与先前报告相比,每位患者平均两次手术的次数较低。

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