Sherer D M, Hulbert W C
Department of Obstetrics and Gynecology, Strong Memorial Hospital, University of Rochester School of Medicine and Dentistry, New York, USA.
Am J Perinatol. 1995 May;12(3):174-7. doi: 10.1055/s-2007-994445.
Prenatal sonographic diagnosis of ureteroceles usually involves clearly duplicated urinary collecting systems associated with ectopic ureters draining the upper renal moieties. We present an unusual case in which an initial sonographic examination was consistent with bilateral orthotopic ureteroceles in association with bilateral single renal systems. The possibility of single systems raised perinatal considerations unique to this anomaly. Repeat prenatal sonography was suggestive of duplex systems and subsequently confirmed as such by neonatal ultrasound and voiding cystourethrogram. At the age of 1 month, the infant underwent bilateral ipsilateral ureteroureterostomy with conservation of the bilateral dilated upper renal moieties. We discuss the possible pathophysiology underlying the different conflicting sonographic findings and address current management of such lesions.
输尿管囊肿的产前超声诊断通常涉及与引流上肾段的异位输尿管相关的明显重复的泌尿系统。我们报告一例罕见病例,最初的超声检查结果提示双侧原位输尿管囊肿合并双侧单肾系统。单肾系统的可能性引发了与该异常相关的围产期特殊考虑。重复产前超声检查提示为重复系统,随后经新生儿超声和排尿性膀胱尿道造影证实。婴儿在1个月大时接受了双侧同侧输尿管输尿管吻合术,保留了双侧扩张的上肾段。我们讨论了不同相互矛盾的超声检查结果背后可能的病理生理学,并阐述了此类病变的当前治疗方法。