Zinner's syndrome: Masquerading as pyonephrotic ectopic kidney

Zinner's syndrome is a rare developmental anomaly of Wolffian duct, comprising a triad of seminal vesicle cyst, ipsilateral renal agenesis and ejaculatory duct obstruction, first described by Zinner in 1914. Several aberrations have been reported like renal dysplasia, ectopic ureteric orifice i...

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Veröffentlicht in:Radiology case reports 2023-01, Vol.18 (1), p.131-134
Hauptverfasser: Ansari, Faiz Manzar, Para, Sajad Ahmad, Singh, Shashank, Wani, Mohammad Saleem, Bhat, Arif Hamid, Maurya, Manjul Kumar
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Sprache:eng
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Zusammenfassung:Zinner's syndrome is a rare developmental anomaly of Wolffian duct, comprising a triad of seminal vesicle cyst, ipsilateral renal agenesis and ejaculatory duct obstruction, first described by Zinner in 1914. Several aberrations have been reported like renal dysplasia, ectopic ureteric orifice in one of the derivatives of Wolffian duct. Usually it presents in second to fourth decade of life with symptoms of urinary bladder irritation/obstruction, cyst distension, ejaculatory duct obstruction. The diagnosis is principally based on imaging studies, usually confirmed by MRI. Treatment is based upon the persistent symptoms or complications related to it. Excision of cyst is gold standard.
ISSN:1930-0433
1930-0433
DOI:10.1016/j.radcr.2022.09.060