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先天性输精管缺如和异位肾。

Congenital absence of vas deferens and ectopic kidney.

作者信息

Salwan Alobaidi, Abdelrahman Alhmooze

机构信息

Dar Al-Salam Hospital, Jordan.

出版信息

Int J Surg Case Rep. 2017;34:90-92. doi: 10.1016/j.ijscr.2017.03.019. Epub 2017 Mar 18.

Abstract

INTRODUCTION

Congenital absence of the vas deferens (CUAVD) is a rare clinical entity, usually discovered accidently during surgical procedures of the urogenital zone, CUAVD has the prevalence of 0.5-1.0% in male population and it is associated with various forms of congenital genitourinary malformations like renal agenesis. we present a case of a 21 years old, male, managed in our private hospital for varicoceles and discovered to have CUAVD and ectopic kidney.

PRESENTATION OF CASE

A 21 years old male, with no significant medical or surgical history presented to our out-patient clinic complaining of scrotal heaviness and pain. upon physical examination he was discovered to have a bilateral varicocele and was scheduled for a bilateral varicocelectomy, during the procedure he was discovered with left side CUAVD.

DISCUSSION

Congenital unilateral absence of the vas deference is a very rare clinical entity in the male population it has an incidence of 0.5-1.0%. it is usually discovered during evaluation for infertility or surgical procedures of the urogenital zone. Unilateral congenital absence of the vas deference is more associated with renal agenesis (73.3%), compared to the bilateral form (11.8%) CAVD is responsible of 1-2% of male infertility.

CONCLUSION

Congenital absence of the vas deference is a unique clinical entity due to its great association with a large variety of urogenital abnormalities, we present this case to stress the importance of including scrotal examination in the routine physical exam to reduce the late diagnosis of such abnormality and it associated comorbidities.

摘要

引言

先天性输精管缺如(CUAVD)是一种罕见的临床病症,通常在泌尿生殖区手术过程中意外发现。CUAVD在男性人群中的患病率为0.5 - 1.0%,并与各种先天性泌尿生殖系统畸形相关,如肾缺如。我们报告一例21岁男性病例,该患者在我们私立医院因精索静脉曲张接受治疗,却被发现患有CUAVD和异位肾。

病例介绍

一名21岁男性,无重大病史或手术史,到我们门诊就诊,主诉阴囊坠胀和疼痛。体格检查发现他患有双侧精索静脉曲张,遂安排进行双侧精索静脉结扎术,术中发现他左侧存在CUAVD。

讨论

先天性单侧输精管缺如在男性人群中是一种非常罕见的临床病症,发病率为0.5 - 1.0%。它通常在评估不育症或泌尿生殖区手术过程中被发现。与双侧形式(11.8%)相比,单侧先天性输精管缺如与肾缺如的关联性更强(73.3%)。CUAVD导致1 - 2%的男性不育症。

结论

先天性输精管缺如是一种独特的临床病症,因其与多种泌尿生殖系统异常密切相关。我们报告此病例是为了强调在常规体格检查中纳入阴囊检查的重要性,以减少此类异常及其相关合并症的漏诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c68/5379864/93e49620097d/gr1.jpg

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