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Seminal Vesicle Infection of Zinner Syndrome Misdiagnosed for Neoplasm
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Young Joo Kim
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Urogenit Tract Infect 2020;15(2):54-56. Published online August 31, 2020
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DOI: https://doi.org/10.14777/uti.2020.15.2.54
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 Abstract
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- 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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Bladder Stone causing Acute Renal Failure and Urinary Tract Infection
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Sung Dae Kim, Young Joo Kim, Jung Sik Huh
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Korean J Urogenit Tract Infect Inflamm 2012;7(2):178-181. Published online October 31, 2012
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Abstract
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- Bladder stones are not a rare disease, but it is rare for such a calculus to be so large as to cause bilateral hydronephrosis. In a previous report, we described an unusual case of spontaneous bladder rupture due to a giant bladder stone. The patient was a 68-year-old man, who had undergone primary repair of bladder rupture and cystolithotripsy of a giant bladder stone with lithoclast at the age of 63 years old. Then he did loss follow-up to the hospital for 5 years. After 5 years, he came back to the hospital with the same symptoms such as decreased urine volume, suprapubic discomfort. Fortunately, the previous treatment which consisted of litholopaxy and antibiotics was effective again. Worldwide, it is the first reported case of recurrent acute renal failure and urinary tract infection after bladder spontaneous rupture due to a giant bladder stone. (Korean J UTII 2012;7:178-181)
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