Author:
Dai Ruijie,Jiang Fan,Fan Junjie,He Dalin,Li Lei,Wu Kaijie
Abstract
Zinner’s syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.
Reference30 articles.
1. Zinner syndrome-a rare developmental anomaly of the mesonephric duct diagnosed on magnetic resonance imaging;Mehra;Radiol Case Rep,2016
2. Zinner's syndrome: clinical features and imaging diagnosis;Jiang;Asian J andrology,2018
3. Cystic dilatations within the pelvis in patients with ipsilateral renal agenesis or dysplasia;Sheih;J Urol,1990
4. Ultrasound diagnosis and treatmentof zinner syndrome: one case report;Liao;J Med Imaging,2021
5. Zinner syndrome: A case report and review of the literature;Cao;Natl J Andrology,2017