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胎儿性尿囊瘤再探。

The fetal urinoma revisited.

机构信息

Department of Women's Imaging University of California, 1600 Divisidero St, Room C-250, San Francisco, CA 94115 USA.

出版信息

J Ultrasound Med. 2014 Jan;33(1):161-6. doi: 10.7863/ultra.33.1.161.

Abstract

The fetal urinoma is a rare but important diagnosis, as it indicates substantial underlying obstruction with implications for the functionality of the affected kidney. This case series describes a single center's experience with the diagnosis and management of fetal urinomas. All 25 cases were diagnosed or referred to our medical center over an 11-year period. Most cases were secondary to either posterior urethral valves or ureteropelvic junction obstruction. Fetal interventions, including percutaneous drainage of the urinoma and cystoscopic alleviation of bladder outlet obstruction, were performed in 4 cases.

摘要

胎儿尿囊瘤是一种罕见但重要的诊断,因为它表明存在实质性的潜在梗阻,这对受影响的肾脏功能有影响。本病例系列描述了单一中心在胎儿尿囊瘤的诊断和治疗方面的经验。在 11 年的时间里,共有 25 例病例被诊断或转至我们的医疗中心。大多数病例继发于后尿道瓣膜或肾盂输尿管连接部梗阻。4 例患者接受了胎儿干预,包括经皮引流尿囊瘤和膀胱镜缓解膀胱出口梗阻。

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