Adult Presentation of Ectopic Vas Deferens with Dysplastic Kidney

نویسندگان

  • Yusuf Saifee
  • Pranjal Modi
چکیده

A 24-year-old male presented with voiding lower urinary tract symptoms. On evaluation, the patient was found to have midbulbar urethral stricture and right dysplastic pelvic kidney with right vesicoureteral reflux. A micturating cystourethrogram (MCUG) shows opacification of the right vas deferens along the entire course till the testis. The patient underwent end-to-end urethroplasty. But soon the patient presented with urinary tract infection (UTI) and epididymorchitis in the follow-up period. The patient was explored laparoscopically to remove dysplastic kidney and ectopic vas deferens. Laparoscopically, the testicular end of the left vas deferens entering the deep inguinal ring was clipped and cut. Also the dysplastic kidney and ureter were removed till the vesicoureteral junction. At 1 year of follow-up, the patient is voiding well with no episodes of UTI.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Congenital absence of vas deferens and ectopic kidney

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 hosp...

متن کامل

A Case of Ectopic Ureterocele

SUMMARY Ureterocele is a cystic dilatation of submucosal segment of intravesical ureter. It Usually classified as "simple" and "ectopic" ureterocele. The simple or adult type has less clinical significance. The most common clinical presentation of ureterocele is recurrent urinary tract infection. Although it may present with other features such as: Sepsis, abdominal pain, failure to thrive, n...

متن کامل

Epididymitis Due to Bilateral Ectopic Vas Deferens and Anorectal Malformation

Recurrent epididymitis and a history of anorectal malformation (ARM) may be secondary to an ectopic vas deferens to ureter described as persistent mesonephric duct syndrome. This is a case of a child with ARM found to have bilateral ectopic ureter to vas connection. The histopathology specimen here would suggest this is an ectopic ureter to vas. In a child with ARM that is undergoing nephrectom...

متن کامل

A Case of Cryptorchidism with Ipsilateral Congenital Unilateral Absence of the Vas Deferens and Contralateral Renal Agenesis

Introduction and Aims. Congenital absence of the vas deferens is an uncommon anomaly and this clinical condition is responsible for up to 1-2% of male infertility. It can be either unilateral or bilateral and the associated anomalies include cryptorchidism, seminal vesicles and ejaculatory ducts anomalies, and renal anomalies such as renal agenesis. We hereby present a case of congenital unilat...

متن کامل

A case of congenital unilateral absence of the vas deferens

BACKGROUND Congenital unilateral absence of the vas deferens occurs in 0.5%-1.0% of males. It has been associated with various genitourinary abnormalities, including renal agenesis. We report a case of congenital unilateral absence of the vas deferens found incidentally during vasectomy in a patient with known unilateral renal agenesis. CASE PRESENTATION A 24-year-old male presented to our ur...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2016