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尿路结石与畸形合并症:壁内部融合的双输尿管。

Combination of urolithiasis and anomaly: Bifid ureter with fusion in the intramural part.

作者信息

Protoshchak Vladimir Vladimirovich, Iglovikov Nikolay Yurievich, Shevnin Maksim Vladimirovich

机构信息

Department and Clinic of Urology, S. M. Kirov Military Medical Academy of the Ministry of Defense of the Russian Federation, St. Petersburg, Russia.

Department of Urology, North-West State Medical University of I. I. Mechnikov, St. Petersburg, Russia.

出版信息

Urol Ann. 2020 Apr-Jun;12(2):196-198. doi: 10.4103/UA.UA_142_19. Epub 2020 Apr 14.

Abstract

Kidney and upper urinary tract anomalies account for 23% of all birth defects. Partial duplication is slightly more prevalent than complete, 70% and 30%, respectively. A very low fusion of ureters, i.e., in the intramural part, is a rarer case. As a result, the joint section is very short (<1 cm) and may be invisible for radiological diagnosis. This case shows a rare variation of incomplete bifid ureter coupled with urolithiasis, which should be taken into account by the physician when determining urolithiasis treatment.

摘要

肾脏和上尿路异常占所有出生缺陷的23%。部分重复比完全重复略为常见,分别为70%和30%。输尿管的极低融合,即在壁内部位,是一种较罕见的情况。因此,联合段非常短(<1厘米),可能在放射学诊断中不可见。本病例显示了不完全双输尿管合并尿路结石的罕见变异,医生在确定尿路结石治疗方案时应予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9685/7292432/803a35b45474/UA-12-196-g001.jpg

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