Abstract：
:Seminal vesicle cysts are usually congenital and frequently accompanied by upper urinary tract abnormalities due to mesonephric duct maldevelopment. Zinner syndrome, first described in 1914, refers to a triad of features consisting of seminal vesicle cysts, ejaculatory duct obstruction, and unilateral (mostly ipsilateral) renal agenesis. We herein present four pediatric patients with Zinner syndrome diagnosed at a children's medical center. A remnant ureteral structure was observed in three (75%) patients. Interestingly, a multicystic dysplastic kidney was present in one (25%) patient before it eventually disappeared. These findings suggest possible involvement of renal dysgenesis rather than agenesis in Zinner syndrome.
journal_name
Urologyjournal_title
Urologyauthors
Takemura K,Sato A,Morizawa Y,Kufukihara R,Iwasa S,Satoh Hdoi
10.1016/j.urology.2020.09.024subject
Has Abstractpub_date
2020-09-28 00:00:00eissn
0090-4295issn
1527-9995pii
S0090-4295(20)31173-0pub_type
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