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Diagnosis of Zinner syndrome: A case of rare occurrence.

Title: Diagnosis of Zinner syndrome: A case of rare occurrence.
Authors: Thinh ND; Department of Radiology, Thanh Nhan Hospital, Hanoi, Vietnam.; Lam VD; Department of Radiology, Thanh Nhan Hospital, Hanoi, Vietnam.; My NTL; Department of Anesthesia and Intensive Care, Thanh Nhan Hospital, Hanoi, Vietnam.; Dung LT; Department of Radiology, Viet Duc University Hospital, Hanoi, Vietnam.; Department of Radiology, University of Medicine and Pharmacy (VNU-UMP), Vietnam National University, Hanoi, Vietnam.; The ND; Department of Radiology, Viet Duc University Hospital, Hanoi, Vietnam.; Loc TQ; Department of Radiology, Viet Duc University Hospital, Hanoi, Vietnam.; Department of Radiology, University of Medicine and Pharmacy (VNU-UMP), Vietnam National University, Hanoi, Vietnam.
Source: Radiology case reports [Radiol Case Rep] 2025 Jul 12; Vol. 20 (10), pp. 4921-4924. Date of Electronic Publication: 2025 Jul 12 (Print Publication: 2025).
Publication Type: Case Reports; Journal Article
Language: English
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101467888 Publication Model: eCollection Cited Medium: Print ISSN: 1930-0433 (Print) Linking ISSN: 19300433 NLM ISO Abbreviation: Radiol Case Rep Subsets: PubMed not MEDLINE
Imprint Name(s): Publication: 2015-: Amsterdam : Elsevier; Original Publication: Seattle, WA : University of Washington, 2006-
Abstract: Zinner syndrome is a rare congenital urinary condition, secondary to disruptions in the embryonic development process between the fourth and 13th week of pregnancy, particularly due to abnormalities in the development of the distal mesonephric duct. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral vas deferens obstruction. We present a case of a young male patient who came to the hospital for a health check-up. A computer tomography scan revealed the absence of the right kidney, dilated vas deferens, and a right seminal vesicle cyst. The patient was advised that there was no indication for surgical intervention and recommended to follow up and monitor the condition after a period of time for re-evaluation.; (© 2025 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
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Contributed Indexing: Keywords: CT scan; Renal agenesis; Urogenital anomalies; Zinner syndrome
Entry Date(s): Date Created: 20250822 Date Completed: 20250914 Latest Revision: 20250914
Update Code: 20260130
PubMed Central ID: PMC12365805
DOI: 10.1016/j.radcr.2025.06.054
PMID: 40843298
Database: MEDLINE

Case Reports; Journal Article