Zinner syndrome: Clinical insights from Western Norway
Emanuel Bjurulf, Lars A R Reisæter, Hemamaalini Rajkumar, Adeel Asghar Chaudhury, Alfred Honoré, Florin Hopland-Nechita, Christian Arvei Moen, Julie Nøss Haugland, Ravi Rawal, Ingunn Roth, Anh Khoi Vo, Christian Beisland, Patrick Juliebø-Jones

TL;DR
This study provides clinical insights into Zinner syndrome, a rare condition affecting the urinary and reproductive systems, based on six cases from Western Norway.
Contribution
The paper presents a multi-case analysis of Zinner syndrome, offering new clinical management insights from real-world cases.
Findings
Zinner syndrome can present with a wide range of symptoms and at varying ages.
Half of the patients were successfully managed with a conservative approach.
Two-thirds of patients had children through natural or assisted methods.
Abstract
Zinner syndrome (ZS) is characterised by unilateral renal agenesis, ipsilateral seminal vesicle cyst and obstruction of the ejaculatory duct. Although rare, urologists may encounter it at some point in their clinical practice. The literature is largely limited to case reports, and the condition is poorly understood. Our objective was to report on cases of ZS that have been managed at two centres in order to gain further clinical insights on this condition. A retrospective review was conducted on ZS cases presenting at two centres in Western Norway between January 2021 and June 2024. Data were collected on demographic details, symptomatology, imaging findings, management and fertility outcomes. Six cases were identified that met the full triad for ZS, with ages ranging from 18 to 70 years. Five patients were symptomatic at presentation, reporting issues such as anejaculation and…
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Taxonomy
TopicsUrologic and reproductive health conditions · Urological Disorders and Treatments · Genital Health and Disease
