Hergan Benedikt, Fellner Franz A, Akbari Kaveh
Central Radiology Institute, Kepler University Hospital, Medical Faculty of the Johannes Kepler University, Krankenhausstrasse 9, Linz, Austria.
Medical Faculty of the Friedrich-Alexander-University of Erlangen-Nürnberg, Erlangen, Germany.
Radiol Case Rep. 2020 Feb 19;15(4):437-441. doi: 10.1016/j.radcr.2020.01.027. eCollection 2020 Apr.
A triad of seminal vesical cyst, ipsilateral renal agenesis and ipsilateral ejaculatory duct obstruction is known as Zinner Syndrome. First described in 1914, only about 200 cases have been reported in literature. Usually it stays undiagnosed until the second to third decade of life due to lack of symptoms or nonspecific symptoms such as lower urinary tract symptoms, dysuria or painful ejaculation. In this report we present the case of a 22-year-old patient with a Zinner syndrome as an incidental finding and underlie a review of literature to show the main clinical and imaging implications.
精囊囊肿、同侧肾缺如和同侧射精管梗阻三联征被称为津纳综合征。该综合征于1914年首次被描述，文献中仅报道了约200例病例。由于缺乏症状或出现如下尿路症状、排尿困难或射精疼痛等非特异性症状，该综合征通常在生命的第二个十年到第三个十年才被诊断出来。在本报告中，我们介绍了一名22岁患有津纳综合征的患者，该病例为偶然发现，并对文献进行了综述，以展示其主要的临床和影像学表现。
