Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/5494
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dc.contributor.authorPatil, Siddanagouda-
dc.date.accessioned2024-06-28T06:49:16Z-
dc.date.available2024-06-28T06:49:16Z-
dc.date.issued2024-
dc.identifier.urihttp://20.193.157.4:9595/xmlui/handle/123456789/5494-
dc.description.abstractEpididymo-orchitis is an inflammatory lesion of the testis and epididymis with a lymphocytic exudate. Patients with acute epididymo-orchitis typically present with scrotal pain, swelling, tenderness and fever. Here, we present a patient with scrotal pain and hemiscrotal swelling as the main complaints; however further investigations revealed a completely different and rare diagnosis. Zinner’s syndrome is a very rare developmental anomaly of the Wolffian duct. To date, only about 200 cases have been diagnosed. It is a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ejaculatory duct obstruction. Some patients remain asymptomatic and discovered incidentally, while others present with symptoms related to seminal vesicle cysts or ejaculatory duct obstruction: voiding or ejaculatory difficulty or pain. Treatment options include transurethral or transrectal aspiration and percutaneous drainage, however both are linked to an increased risk of recurrence. Symptomatic, complicated and recurrent cyst will require excision of the cyst, either laparoscopically or robotically.en_US
dc.language.isoenen_US
dc.publisherBLDE(DU)en_US
dc.subjectEpididymo-orchitisen_US
dc.subject, Orchitis, Zinner syndromeen_US
dc.titleA rare cause of epididymo-orchitisen_US
dc.typeArticleen_US
Appears in Collections:Faculty of Urology

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