ArticleCase reports in urology2020
Zinner's Syndrome: A Rare Diagnosis of Dysuria Based on Imaging.
Article in Case reports in urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 11 citations in OpenAlex.
- Zinner syndrome, a rare congenital urogenital tract malformation: the first reported case in Indonesia.Fukushima journal of medical science · 2025Article
- Zinner syndrome: A mesonephric duct anomaly with renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction.Medical journal, Armed Forces India · 2024Article
- Potential pharmacotherapy for Zinner syndrome.Translational andrology and urology · 2023Article
- Clinicopathological and genetic features of Zinner's syndrome: two case reports and review of the literature.Frontiers in urology · 2023Article
- Magnetic resonance urography of congenital abnormalities - what the radiologist needs to know.Pediatric radiology · 2022Article
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Authors and funding
8 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zinner's syndrome is a rare congenital malformation of the seminal vesicle and ipsilateral upper urinary tract, due to developmental arrest in early embryogenesis of the Müllerian duct. Clinical presentation is nonspecific and includes voiding symptoms such as dysuria, ejaculatory disorders, and hypogastric or perineal pain. The diagnosis is made with imaging techniques, notably Magnetic Resonance Imaging (MRI) which remains the gold standard exam for diagnosis confirmation and therapeutic management. Treatment options depend on the severity of symptoms, the size of the cyst, and the complications. Herein, we report a rare case of a 33-year-old young patient who presented recurrent dysuria and ejaculatory disorders for the last 5 years. Imaging studies revealed an empty left renal fossa, with cystic pelvic mass related to the seminal vesicle and which was compatible with the diagnosis of Zinner's syndrome. The patient underwent successful laparoscopic removal of the cyst and seminal vesicle, with total disappearance of urinary and sexual complaints with a 3-year follow-up.
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Registered trials
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