Abstract
Until now, fewer than 60 cases of tumors originating from the seminal vesicle have been reported. Most of them were adenocarcinoma, cystadenoma, and benign mesenchymal tumor [1]. Among them, only three cases in the English literature have been reported as squamous cell carcinoma [2-4]. Although all three cases had a prolonged history of stone formation or chronic inflammation, none of them were associated with congenital malformation of the urogenital system such as Zinner syndrome. Zinner syndrome is a rare Mullerian duct abnormality consisting of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. Herein, we report a 41-year-old male with Zinner syndrome, who developed a poorly differentiated squamous cell carcinoma of the seminal vesicle as a result of prolonged inflammation.
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