Author(s):
1. ASLAM S:
Department of Radiology, Multan Institute of Kidney Diseases, Pakistan.
2. NASREEN M:
Department of Radiology, Mukhtar A Sheikh Hospital, Multan, Pakistan
3. HAMEED A:
Department of Urology, Multan Institute of Kidney Diseases, Pakistan
Abstract:
Zinner's syndrome is a rare congenital mesonephric (Wolffian) duct anomaly due to developmental arrest in early embryogenesis, comprising unilateral ejaculatory duct obstruction or agenesis, ipsilateral seminal vesicle cysts, and ipsilateral renal agenesis. Here, we present a case of a healthy 17-year-old male in Pakistan presenting with complaints of mild, dull pain in the left lower abdomen. He had no history of lower urinary tract symptoms and regular bowel habits. Imaging revealed nonvisualization of the left kidney with multi-cystic pelvic mass related to the left seminal vesicle in keeping with the diagnosis of Zinner's syndrome.
Page(s):
1-3
Published:
Journal: Biological and Clinical Sciences Research Journal, Volume: 4, Issue: 1, Year: 2023
Keywords:
Congenital Anomaly
,
Renal Agenesis
,
Unilateral Ejaculatory Duct Obstruction
,
Zinners Syndrome
References:
References are not available for this document.
Citations
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