Zinner综合征的诊断：一例罕见的病例

Q4 Medicine

Radiology Case Reports Pub Date : 2025-07-12 DOI:10.1016/j.radcr.2025.06.054

Nguyen Duy Thinh , Vu Duy Lam , Nguyen Thi Le My , Le Thanh Dung , Nguyen Dinh The , Tran Quang Loc

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引用次数: 0

摘要

Zinner综合征是一种罕见的先天性泌尿系统疾病，继发于妊娠第4周至第13周期间胚胎发育过程的中断，特别是由于远端肾中膜管发育异常。其特征为单侧肾发育不全、同侧精囊囊肿和同侧输精管梗阻。我们提出一个年轻的男性病人谁来医院进行健康检查的情况。计算机断层扫描显示右侧肾脏缺失，输精管扩张，右侧精囊囊肿。告知患者无手术指征，建议随访监测一段时间后重新评估病情。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Diagnosis of Zinner syndrome: A case of rare occurrence

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.

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来源期刊

Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging

CiteScore

1.10

自引率

0.00%

发文量

1074

审稿时长

30 days

期刊介绍： The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.