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Case Report
Seminal Vesicle Infection of Zinner Syndrome Misdiagnosed for Neoplasm
Young Joo Kim
Urogenit Tract Infect 2020;15(2):54-56.   Published online August 31, 2020
DOI: https://doi.org/10.14777/uti.2020.15.2.54
AbstractAbstract PDFPubReaderePub
Zinner syndrome is a rare Müllerian duct congenital anomaly representing unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. A 16-year-patient presented with dysuria, nocturia, and enduring diffuse perineal pain for two months. Radiologic studies revealed a right seminal vesicle cyst with a mass lesion and right renal agenesis. Ultrasonography guided transrectal biopsy indicated a seminal vesicle neoplasm. The mass was diagnosed as chronic inflammation. This paper reports a case of seminal vesicle inflammation associated with Zinner syndrome that was initially misdiagnosed as a neoplasm.
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