ArticleRadiology case reports2026
Zinner syndrome: Case report and brief review of the literature.
Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Zinner Syndrome: A Narrative Review of Imaging Findings with an Illustrative Case Report.Diagnostics (Basel, Switzerland) · 2026Review
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zinner syndrome (ZS) is a rare congenital anomaly of the mesonephric (Wolffian) duct, classically defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. Fewer than 300 cases have been reported in the literature, with most diagnosed in childhood or early adulthood. We present the case of a 17-year-old male who underwent imaging after a syncopal episode, which incidentally revealed inferior vena cava duplication, right renal agenesis, and right-sided cystic dilatation of the seminal vesicle. This case demonstrates radiologic features of ZS and offers a brief review in the embryology, clinical presentation, and management of this syndrome.
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