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 inIJU case reports Vol. 8; no. 4; pp. 322 - 325
Main Authors Patil, Tejasvi, Verma, Amogh, Sachdeva, Rajat, Kumar, Shubham, Gaidhane, Shilpa, Sah, Sanjit, Satapathy, Prakasini, Mehta, Rachana, Simiyu, Benjamin Wafula, Suresh, Vinay
Format Journal Article
LanguageEnglish
Published Australia John Wiley & Sons, Inc 01.07.2025
John Wiley and Sons Inc
Wiley
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ISSN2577-171X
2577-171X
DOI10.1002/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.
Bibliography:Amogh Verma and Tejasvi Patil contributed equally and are the co‐first authors.
The authors received to specific funding for this work.
Funding
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Funding: The authors received to specific funding for this work.
ISSN:2577-171X
2577-171X
DOI:10.1002/iju5.70029