scholarly journals Seminal Vesicle Cyst And Renal Agenesia Case With Abdominal Pain

2014 ◽  
Vol 24 (2) ◽  
pp. 127-130
Author(s):  
Hakan Türk ◽  
Sıtkı Ün ◽  
Cemal Selçuk İşoğlu ◽  
Özgür Çakmak ◽  
Hüseyin Tarhan ◽  
...  
1983 ◽  
Vol 19 (1) ◽  
pp. 257
Author(s):  
C S Song ◽  
J H Park ◽  
C W Kim

2017 ◽  
Vol 1 (2) ◽  
pp. 81
Author(s):  
Abdulaziz Alharbi ◽  
Sultan Alammari ◽  
Refaat Salman ◽  
Yousof Alzahrani

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Niall P. Kelly ◽  
Adrian Fuentes-Bonachera ◽  
William P. Shields ◽  
Ivor M. Cullen ◽  
Padraig J. Daly

Zinner syndrome was first described in 1914 and represents the triad of unilateral renal agenesis and ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Seminal vesicle cysts are often asymptomatic but can also present with pain, haematospermia, or other lower urinary tract symptoms. Treatment strategies include observation and surgical excision. We present the laparoscopic management of an enlarged seminal vesicle cyst, consistent with Zinner syndrome, 14 years after the initial diagnosis. A 58-year-old male patient was diagnosed with a left-sided seminal vesicle cyst while undergoing assessment for renal transplant due to progressively worsening renal function in his solitary right kidney. The otherwise asymptomatic cyst enlarged from the time of initial diagnosis in 2004 ( 11.3   cm × 9.7   cm × 13.1   cm ) to nearly double the size in 2018 ( 12.8   cm × 11.9   cm × 14.2   cm ). This cyst size ultimately precluded renal transplant, and the patient was referred for excision. Laparoscopic excision of the cyst was performed, histopathology confirmed seminal vesicle cyst tissue, and there has been no recurrence of the cyst to date. The patient remains active on the renal transplant waitlist. Zinner syndrome is a rare syndrome, with the seminal vesicle cysts being managed by observation or surgical excision. We report the longest documented observation of a seminal vesicle cyst, culminating in a safe and successful laparoscopic excision.


2008 ◽  
Vol 75 (2) ◽  
pp. 122-126 ◽  
Author(s):  
Kenji Ohgaki ◽  
Kazutaka Horiuchi ◽  
Fumiatsu Oka ◽  
Mitsuhiro Sato ◽  
Taiji Nishimura

2016 ◽  
Vol 52 (5) ◽  
pp. 335-340 ◽  
Author(s):  
Maria Ardiaca ◽  
Cristina Bonvehi ◽  
Marina Cuesta ◽  
Alicia Gomez ◽  
Andres Montesinos

ABSTRACT To date, descriptions of pathologic conditions of the seminal vesicle in rabbits are scarce and limited to the laboratory animals in experimental conditions. The present article describes three cases of strangury, abdominal pain, and anorexia associated with seminal vesiculitis in pet rabbits. Three non-neutered male pet rabbits aged 3.6, 1.5, and 2.1 yrs were presented with strangury, abdominal pain, and anorexia. Seminal vesiculitis was diagnosed based on clinical signs and ultrasonography findings. Vesiculectomy was performed in two cases that presented strangury refractory to medical treatment, and diagnosis was confirmed by histopathology. In the third case, the patient received medical treatment, and a sequela in the form of lithiasis of the seminal vesicle was detected 3 yrs later. Plain radiographs were nearly unremarkable, and results from complete blood analysis and urinalysis were not specific in all three cases. Contrast radiography was performed in one case, showing a dilated seminal vesicle. Ultrasound and surgical biopsy seem to be the most sensitive techniques in the diagnosis of this pathology. Seminal vesiculitis must be included in the differential diagnosis of acute or chronic strangury in male pet rabbits.


1969 ◽  
Vol 62 (5) ◽  
pp. 608-610 ◽  
Author(s):  
ALAN C. DAVIDSON ◽  
MAJ JEFF H. BEARD

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