ArticleUrology case reports2025
Zinner syndrome incidentally diagnosed in a man with ureteropelvic junction stone and hydronephrosis: A case report.
Article in Urology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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2 citing papers in PubMed.
- Zinner syndrome: Case report and brief review of the literature.Radiology case reports · 2026Article
- Zinner syndrome: unilateral renal agenesis with unique findings in a 19-year-old patient from Pakistan - a case report with literature review.Annals of medicine and surgery (2012) · 2025Article
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5 authors.
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Abstract
Zinner syndrome is a congenital anomaly characterized by seminal vesicle cysts, ipsilateral renal agenesis, and ejaculatory duct obstruction possibly associated with infertility. Only 200 cases of Zinner syndrome have been reported since its discovery in 1914. We present the case of a 63-year-old man seeking treatment for a ureteropelvic junction stone causing severe hydronephrosis. After the patient's history and the computed tomography findings were reviewed, the diagnosis of Zinner syndrome was confirmed. The patient has been nearly asymptomatic and has had three children during his lifetime. Our case could serve as a reference for future diagnoses of this rare anomaly.
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