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Generation and Quantitative Characterization of Functional and Polarized Biliary Epithelial Cysts
Published on: May 16, 2020
Cysts of the ejaculatory system: a report of two cases
Toshihiro Yanai1, Tadaharu Okazaki, Atsuyuki Yamataka
1Department of Pediatric General and Urogenital Surgery, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. t-yanai@med.juntendo.ac.jp
Insights
Rare cystic dilatations of the ejaculatory system can cause recurrent epididymo-orchitis (E-O) in children. Early diagnosis and appropriate management, including vasoligation, are crucial for successful outcomes.
Area of Science:
- Pediatric Urology
- Reproductive Medicine
- Surgical Pathology
Background:
- Cystic dilatations of the ejaculatory system are rare congenital anomalies.
- Recurrent epididymo-orchitis (E-O) in prepubertal children can have various etiologies.
Observation:
- Two cases of prepubertal boys with recurrent E-O are presented.
- Both cases involved retrovesical cysts associated with ejaculatory duct abnormalities.
- Case 1 had a fused ejaculatory duct and seminal vesicle mass with cystic dilatation; Case 2 had a cyst communicating with the ejaculatory ducts and causing vasal reflux.
Findings:
- Surgical excision of the ejaculatory duct cyst with vasoligation resolved symptoms in Case 1.
- Vasoligation alone, without cyst excision, successfully managed recurrent E-O in Case 2.
- Histopathology in Case 1 revealed a metaplastic epithelial lesion within the cyst.
Implications:
- Cysts of the ejaculatory system should be considered in the differential diagnosis of recurrent E-O in young children.
- A high index of suspicion and appropriate diagnostic imaging are recommended for timely diagnosis.
- Management strategies may involve cyst excision or vasoligation, depending on the specific anatomy and presentation.
Abstract:
We report two cases of rare cystic dilatations of the ejaculatory system. In case 1, a 6-month-old boy was referred to us for the management of recurrent epididymo-orchitis (E-O) complicating open drainage and a colostomy was performed elsewhere for a purulent rectal discharge thought to be rectal duplication. Diagnostic imaging showed a retrovesical cyst. Urethrocystoscopy showed a swelling of the verumontanum. No fistula was seen between the cyst and rectum on colonoscopy. At laparotomy, both ejaculatory ducts and seminal vesicles were found to be fused into a mass with cystic dilatation of the ejaculatory duct. Intraoperative histopathology of the cyst identified a metaplastic epithelial lesion. The cyst was excised with bilateral vasoligation. Since surgery, 8 years ago, urination and defecation have been normal. In case 2, a 4-month-old boy presented with fever and a swollen right scrotum. Ultrasonography showed a retrovesical cyst. Right grade IV vesicoureteral reflux diagnosed on voiding cystourethrography was treated by ureter reimplantation (Cohen) but complicated by recurrent E-O. Urethrocystoscopy with retrograde contrast via the utriculus showed that the cyst opened on the verumontanum, that both ejaculatory ducts opened into the cyst, and there was reflux into the right vas deferens. Right vasoligation alone was performed through a scrotal approach. Although the cyst was not excised, there has been no recurrence of E-O nor enlargement of the cyst for 6 years. Cysts of the ejaculatory system should be considered in the etiology of recurrent E-O in prepubertal children and a high index of awareness is recommended.
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