ArticleEuropean journal of pediatric surgery reports2015
Congenital Seminal Vesicle Cyst and Ipsilateral Renal Agenesis (Zinner Syndrome): A Rare Association and Its Evolution from Early Childhood to Adolescence.
Article in European journal of pediatric surgery reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 29 citations in OpenAlex.
- Zinner Syndrome: A Narrative Review of Imaging Findings with an Illustrative Case Report.Diagnostics (Basel, Switzerland) · 2026Review
- Zinner syndrome in pediatric patients: rare disease leading to challenging management.Frontiers in pediatrics · 2024Article
- A rare presentation of Zinner syndrome as recurrent epididymitis: A case report.SAGE open medical case reports · 2023Article
- [And there was Zinner's syndrome-a rare differential diagnosis].Urologie (Heidelberg, Germany) · 2022Article
- A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome-A Case Report.The Indian journal of radiology & imaging · 2021Article
- Long-Term Surveillance and Laparoscopic Management of Zinner Syndrome.Case reports in urology · 2021Article
- Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report.Radiology case reports · 2020Article
- Incidental finding of Zinner syndrome in a Greek military recruit: a case report of a rare clinical entity.Military Medical Research · 2019Article
- Zinner Syndrome in Pediatric Age: Issues in the Diagnosis and Treatment of a Rare Malformation Complex.Frontiers in pediatrics · 2019Article
- OHVIRA and OSVIRA syndrome.The Indian journal of radiology & imagingArticle
- A rare case of abdominal pain.Autopsy & case reportsArticle
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zinner syndrome, the association of congenital seminal vesicle cyst and ipsilateral renal agenesis, is more often reported in adults or older adolescents. We present a case of a boy, followed up in our hospital since birth for right renal agenesis who at the age of 4 years presented a right paravesical cyst on ultrasound. The cyst was initially considered as an ureterocele. The diagnosis of Zinner syndrome was made later, at the age of 15 years by ultrasound and magnetic resonance imaging; at that moment the cyst had increased in size and had changed in aspect. This malformation should be considered in the differential diagnosis of a pelvic cyst in male patients with renal agenesis.
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