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女童双侧单系统异位输尿管伴阴道开口,一种罕见变异型

Bilateral Single System Ectopic Ureters With Vaginal Insertion in a Female Child, A Rare Variant.

作者信息

Patel Mishal, Parikh Urvish, Shrotriya Radhika, Kadam Spandan, Shah Jainam, Chandna Sudhir

机构信息

Pediatric Surgery Department, SVPIMSR and Smt. NHL municipal medical college, Ellisbridge, Ahmedabad, India.

Pediatric Surgery Department, SVPIMSR and Smt. NHL municipal medical college, Ellisbridge, Ahmedabad, India.

出版信息

Urology. 2021 Mar;149:e37-e39. doi: 10.1016/j.urology.2020.10.025. Epub 2020 Oct 28.

Abstract

In most cases an ectopic ureter is associated with a duplicated renal collecting system while in only a few single systems is found. Bilateral single system ureteral ectopia is even rarer. A 9-year-old girl presented with urinary incontinence. Investigations pointed towards bilateral single system ectopic ureters with ectopic openings into vagina with a hypoplastic bladder. The left ureteric system was tortuous with malrotated and hypoplastic left kidney. A 4 × 2 cm hard calculus was found in the vagina. Right Ureteric reimplantation with left to right uretero-ureterostomy was done with satisfactory postoperative day time continence at 6 months without the need for bladder reconstruction or urinary diversion.

摘要

在大多数情况下,异位输尿管与重复肾集合系统相关,而仅有少数发生于单一系统。双侧单一系统输尿管异位更为罕见。一名9岁女孩因尿失禁就诊。检查发现双侧单一系统异位输尿管,异位开口于阴道,膀胱发育不全。左侧输尿管系统迂曲,左肾旋转不良且发育不全。在阴道内发现一枚4×2 cm的硬结石。行右侧输尿管再植术并左至右输尿管输尿管吻合术,术后6个月日间控尿情况良好,无需膀胱重建或尿流改道。

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