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Management Strategies for Seminal Vesicle Cysts in Zinner Syndrome: Insights From Two Cases
Fadhel Yusuf1, Abdulla Husain2, Zuhair Sikafi3
1Urology, Dubai Hospital, Dubai, ARE.
Cureus
|August 6, 2025
Summary
Zinner syndrome, a rare congenital condition, presents unique management challenges. This study shows conservative observation and minimally invasive robotic surgery are effective for symptomatic patients.
Area of Science:
- Urology
- Congenital Malformations
- Male Reproductive System Disorders
Background:
- Zinner syndrome is a rare congenital genitourinary malformation.
- It involves unilateral renal agenesis, seminal vesicle cysts, and ejaculatory duct obstruction.
- Symptoms typically manifest in the third or fourth decade of life.
Observation:
- Two cases of Zinner syndrome with distinct clinical presentations and management strategies were analyzed.
- One patient with mild symptoms was managed conservatively with observation.
- A second patient, refractory to medical therapy, underwent successful robotic-assisted laparoscopic vesiculectomy.
Findings:
- Conservative management can be effective for select patients with mild Zinner syndrome.
- Minimally invasive robotic surgery offers a safe and effective treatment option for symptomatic Zinner syndrome.
- Both approaches led to significant symptom improvement in the presented cases.
Implications:
- These cases underscore the importance of individualized treatment plans for Zinner syndrome.
- Minimally invasive techniques are viable for managing Zinner syndrome, reducing patient morbidity.
- Further research into optimal management strategies for this rare condition is warranted.
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