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在一名患有睾丸非精原细胞瘤的患者中偶然发现辛纳综合征。

Incidental detection of Zinner syndrome in a patient with nonseminomatous germ cell tumor of testis.

作者信息

Khoda Jeevitesh, Sen Saugata, Chatterjee Argha

机构信息

Department of Radiology, Tata Medical Center, Kolkata, West Bengal, India.

出版信息

Urol Ann. 2020 Oct-Dec;12(4):394-395. doi: 10.4103/UA.UA_11_20. Epub 2020 Oct 15.

Abstract

Zinner syndrome is a rare congenital abnormality occurring in males comprising a triad of unilateral renal agenesis, ipsilateral ejaculatory duct obstruction, and seminal vesicle cyst. Most patients remain asymptomatic, and some may present with lower urinary tract symptoms or infertility. We present a case of incidentally detected Zinner syndrome in a patient with nonseminomatous germ cell tumor of testis, an association that is not reported in literature to our knowledge.

摘要

津纳综合征是一种发生于男性的罕见先天性异常,由单侧肾缺如、同侧射精管梗阻和精囊囊肿三联征组成。大多数患者无症状,部分患者可能出现下尿路症状或不育。我们报告一例在睾丸非精原细胞瘤患者中偶然发现的津纳综合征病例,据我们所知,这种关联在文献中尚未有报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/934f/7992532/1c72f026040a/UA-12-394-g001.jpg

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