ArticleCase reports in radiology2024
Zinner Syndrome: The Diagnosis and Management of a Rare Urogenital Malformation.
Article in Case reports in radiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Rare variant of Zinner syndrome with ectopic seminal vesicle and prostatic hypoplasia: A case report.Radiology case reports · 2026Article
- Zinner syndrome: Case report and brief review of the literature.Radiology case reports · 2026Article
- Zinner syndrome, a rare congenital urogenital tract malformation: the first reported case in Indonesia.Fukushima journal of medical science · 2025Article
- Diagnosis of Zinner syndrome: A case of rare occurrence.Radiology case reports · 2025Article
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Authors and funding
5 authors.
Funding
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Abstract
This case highlights an atypical but important consideration in young males presenting with persistent gastrointestinal and/or genitourinary symptoms. Zinner syndrome (ZS) develops from embryologic maldevelopment of the distal mesonephric duct, resulting in ejaculatory duct atresia with consequent obstruction of the seminal vesicle and concomitant ureteral bud malformation, leading to renal agenesis/dysplasia. The lack of distinct clinical symptoms makes ZS a difficult diagnosis to reach: Abdominal pain and dysuria are often mistaken for prostatitis or cystitis. However, the use of modern imaging modalities aids in establishing the diagnosis. Early identification of ZS may delay progression to infertility as the duct obstruction may not be as extensive, though further research is needed to establish this connection.
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Registered trials
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