Suppr超能文献

[产前诊断的先天性泌尿系统畸形的围产期管理]

[Perinatal management of congenital anomalies of the urinary tract detected in utero].

作者信息

Shimada K, Taguchi K, Hosokawa S, Ogino T, Ikoma F

机构信息

Department of Urology, Hyogo College of Medicine.

出版信息

Nihon Hinyokika Gakkai Zasshi. 1990 Jan;81(1):122-9. doi: 10.5980/jpnjurol1989.81.122.

Abstract

The routine use of maternal ultrasonography has led to frequent discovery of fetal anatomical abnormalities of the urinary tract. Herein we report on 35 cases with congenital urogenital anomalies which were found during the last 5 years by the prenatal ultrasonography and referred to our clinic either for treatment or consultation. 1. Findings of prenatal ultrasonography There were 12 cases of hydronephrosis, 7 of multicystic dysplastic kidney, 4 of megaureter, 3 of posterior urethral valve, 2 of ureterocele, 2 of vesicoureteral reflux and 5 other cases. Fetal anomalies were diagnosed during routine maternal examination, as intrauterine growth retardation, oligohydramnios, or the recurrent risk secondary to genetic risk factor or previous abnormal pregnancies. Prenatal diagnosis was made as early as 20 weeks of gestation in a case of hypoplastic urethra with large bladder diverticula. In about 30% of cases, abnormalities were found before 30 weeks of gestation. Oligohydramnios was evident in 5 cases. Prenatal diagnosis was correct in about 60% of cases. In the remainder the diagnosis was either incomplete or incorrect. Errors in the diagnosis resulted from difficulties in the differentiation of dilated ureter, intestinal dilation or intraperitoneal cystic masses. 2. Management in newborn periods Of the patients, 12 were treated urologically in newborn periods. Although patients with distended bladder and dilatation of upper tracts first underwent therapeutic placement of the urethral catheter, upper tract diversion with nephrostomy or tubeless ureterocutaneostomy was required in 2 because of continued elevation of serum creatinine levels. In 2 neonates nephrectomy was indicated for unilateral multicystic kidney, because the large cystic mass might compress the intestine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

孕妇超声检查的常规应用导致胎儿泌尿系统解剖异常被频繁发现。在此,我们报告过去5年通过产前超声检查发现并转诊至我院进行治疗或咨询的35例先天性泌尿生殖系统异常病例。1. 产前超声检查结果:肾盂积水12例,多囊性发育不良肾7例,巨输尿管4例,后尿道瓣膜3例,输尿管囊肿2例,膀胱输尿管反流2例,其他5例。胎儿异常在常规产检时被诊断,表现为宫内生长受限、羊水过少,或因遗传危险因素或既往异常妊娠而存在复发风险。一例尿道发育不全伴巨大膀胱憩室的病例在妊娠20周时即做出产前诊断。约30%的病例在妊娠30周前发现异常。5例有明显羊水过少。约60%的病例产前诊断正确。其余病例诊断不完整或错误。诊断错误是由于难以区分扩张的输尿管、肠道扩张或腹腔内囊性肿物。2. 新生儿期的处理:患者中有12例在新生儿期接受了泌尿外科治疗。虽然膀胱扩张和上尿路扩张的患者首先进行了尿道导管的治疗性置入,但由于血清肌酐水平持续升高,2例患者需要进行肾造瘘或无管输尿管皮肤造口术进行上尿路改道。2例新生儿因单侧多囊肾而进行了肾切除术,因为巨大的囊肿可能压迫肠道。(摘要截短至250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验