Zinner Syndrome

Abakar, Djidda and Badi, Fatima-Ezzahrae and Sabiri, Mouna and El Manjra, Samia and Lezar, Samira and Essodegui, Fatiha (2021) Zinner Syndrome. European Journal of Case Reports in Internal Medicine, 8 (6). pp. 1-3. ISSN ISSN: 2284-2594

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Abstract

Zinner syndrome is a developmental anomaly of the urogenital tract. This condition is defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. The syndrome is due to malformation of the mesonephric duct during embryogenesis. The condition used to be rare but is now frequently encountered due to the advent of MRI and CT. MRI confirms the diagnosis by revealing the seminal vesicle cyst and its contents, and the ejaculatory duct obstruction, while CT confirms renal agenesis. We report the case of a young patient with Zinner syndrome.

Item Type: Article
Uncontrolled Keywords: Zinner syndrome, seminal vesicle cyst, renal agenesis
Subjects: 600 Tecnologia - Scienze applicate
600 Tecnologia - Scienze applicate > 610 Medicina e salute (Classificare qui la tecnologia dei servizi medici)
600 Tecnologia - Scienze applicate > 610 Medicina e salute (Classificare qui la tecnologia dei servizi medici) > 616 Malattie (classificare qui la Clinica medica, la medicina basata sull'evidenza, la Medicina interna, la Medicina sperimentale)
Depositing User: Marina Spanti
Date Deposited: 25 Jan 2022 15:39
Last Modified: 25 Jan 2022 15:39
URI: http://eprints.bice.rm.cnr.it/id/eprint/21271

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