A case with an ectopic ejaculatory duct opening into the bladder trigone in Zinner syndrome, congenital unilateral renal agenesis, and an ipsilateral seminal vesicle cyst

Q4 Medicine IJU Case Reports Pub Date : 2024-07-30 DOI:10.1002/iju5.12763
Taiju Hyuga, Kazuya Tanabe, Taro Kubo, Kimihiko Moriya
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Abstract

Introduction

This report describes a case with an ectopic ejaculatory duct opening into the bladder trigone in Zinner syndrome, congenital unilateral renal agenesis, and an ipsilateral seminal vesicle cyst.

Case presentation

The patient was identified when no left kidney was detected in the fetal period. Abdominal ultrasonography and pelvic plain MRI at 6 months old revealed a 10-mm cystic lesion on the dorsal aspect of the bladder. Cysto-urethroscopy at 1 year old revealed a rather short posterior urethra and right and left inferior crests extending from the posterior urethra beyond the bladder neck. The ejaculatory duct opening was identified on the bladder trigone.

Conclusion

Anatomical abnormality of the ejaculatory duct may represent a cause of infertility and ejaculatory dysfunction in Zinner syndrome. Endoscopic evaluation should be performed for this rare anomaly, even in children.

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一例 Zinner 综合征患者的异位射精管开口于膀胱三叉神经、先天性单侧肾发育不全和同侧精囊囊肿。
导言:本报告描述了一例患有 Zinner 综合征的异位射精管开口于膀胱三叉神经、先天性单侧肾脏发育不全和同侧精囊囊肿的病例:患者是在胎儿时期发现没有左肾的。6个月大时,腹部超声波检查和盆腔核磁共振成像(MRI)显示膀胱背侧有一个10毫米的囊肿病灶。1 岁时进行的膀胱尿道镜检查发现后尿道相当短,左右下嵴从后尿道延伸至膀胱颈外。射精管开口位于膀胱三叉神经上:结论:射精管的解剖异常可能是导致齐纳综合征患者不育和射精功能障碍的原因之一。对于这种罕见的异常,即使是儿童也应进行内窥镜评估。
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来源期刊
IJU Case Reports
IJU Case Reports Medicine-Urology
CiteScore
0.60
自引率
0.00%
发文量
147
审稿时长
15 weeks
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