SURGICAL TREATMENT FOR PELVIC DYSTOPIA OF THE LEFT HYPOPLASTIC KIDNEY WITH VAGINAL ECTOPIA OF THE URETER

I. V. Feofilov, S. S. Shkuratov, A.K. Pochivalov
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Abstract

Among the anomalies in the development of all organs and systems, congenital malformations of the kidneys and upper urinary tract occupy the first place, accounting for 12.9–40% of all congenital malformations and 3–5.5% of the total number of urological cases. The combination of two or more anomalies of the genitourinary system is extremely rare. The article presents a description of the clinical observation and the choice of surgical treatment for three anomalies in the development of the urinary system, for a long time unrecognized in a 19-year-old patient — pelvic dystopia of the left hypoplastic kidney with vaginal ectopia of the ureter.
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左肾发育不全伴阴道输尿管异位的盆腔难产的手术治疗
在所有器官和系统发育异常中,肾脏和上尿路先天性畸形占首位,占所有先天性畸形的12.9-40%,占泌尿外科病例总数的3-5.5%。泌尿生殖系统两种或两种以上异常的结合是极其罕见的。本文描述了一位19岁患者的临床观察和手术治疗的选择,这三种泌尿系统发育异常,长期未被认识-左肾发育不全盆腔难产伴输尿管阴道异位。
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