Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract

Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infert...

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Detalles Bibliográficos
Autores principales: Almuhanna, Ahmed M., Alsuhaibani, Shaheed, Almesned, Razan, Almatar, Ashraf, Alali, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Endrology & Infertility
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455976/
https://www.ncbi.nlm.nih.gov/pubmed/34584848
http://dx.doi.org/10.1016/j.eucr.2021.101839
Descripción
Sumario:Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infertility. Herein we are highlighting a case of a 35 years-old male, a father of 4 biological children who presented to our clinic due to right hemiscrotal pain, associated with post ejaculation pain.

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