Zinner Syndrome Presenting With Chronic Pelvic Pain and Ejaculatory Dysfunction
ABSTRACT Introduction Zinner Syndrome is a rare congenital anomaly involving unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. We report a symptomatic case managed conservatively. Case Presentation A 19‐year‐old male presented with 6 months of intermitten...
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Published in | IJU case reports Vol. 8; no. 4; pp. 322 - 325 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Australia
John Wiley & Sons, Inc
01.07.2025
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2577-171X 2577-171X |
DOI | 10.1002/iju5.70029 |
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Summary: | ABSTRACT
Introduction
Zinner Syndrome is a rare congenital anomaly involving unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. We report a symptomatic case managed conservatively.
Case Presentation
A 19‐year‐old male presented with 6 months of intermittent pelvic pain, dysuria, and ejaculatory discomfort. Examination was unremarkable. Ultrasonography showed right renal agenesis and a pelvic cyst. MRI confirmed a 2.8 cm cystic dilatation of the right seminal vesicle with vas deferens dilatation and absent right kidney. No ectopic renal tissue was seen. Semen analysis revealed oligospermia. Given mild symptoms and fertility concerns, he was treated conservatively with NSAIDs and antibiotics, resulting in symptom improvement within 4 weeks. Surveillance was planned.
Conclusion
Zinner Syndrome should be considered in young males with unexplained pelvic or ejaculatory symptoms. MRI is essential for accurate diagnosis. Conservative treatment is suitable for mild cases, reserving surgery for progressive symptoms or fertility issues. |
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Bibliography: | Amogh Verma and Tejasvi Patil contributed equally and are the co‐first authors. The authors received to specific funding for this work. Funding ObjectType-Case Study-2 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Report-1 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 Funding: The authors received to specific funding for this work. |
ISSN: | 2577-171X 2577-171X |
DOI: | 10.1002/iju5.70029 |