Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report

Abstract Background Zinner’s syndrome is a rare congenital malformation involving the seminal vesicle that mostly shows cystic transformation. Embryogenesis of the kidney, ureter, seminal vesicle, and vas deferens can be altered if an insult occurs during the first trimester mainly between the 4th a...

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Main Authors: Ahmed Atef Soliman, Anwar Ali Alshukami, Walaa Hussein AlZuber
Format: Article
Language:English
Published: SpringerOpen 2020-10-01
Series:The Egyptian Journal of Radiology and Nuclear Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s43055-020-00336-6
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spelling doaj-131bee6eb1144ee9896264d39f5f8fcc2020-11-25T03:35:58ZengSpringerOpenThe Egyptian Journal of Radiology and Nuclear Medicine2090-47622020-10-015111410.1186/s43055-020-00336-6Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case reportAhmed Atef Soliman0Anwar Ali Alshukami1Walaa Hussein AlZuber2Radiology Department, King Khalid HospitalRadiology Department, King Khalid HospitalRadiology Department, King Khalid HospitalAbstract Background Zinner’s syndrome is a rare congenital malformation involving the seminal vesicle that mostly shows cystic transformation. Embryogenesis of the kidney, ureter, seminal vesicle, and vas deferens can be altered if an insult occurs during the first trimester mainly between the 4th and the 13th gestational week. Cystic lesions of the seminal vesicle may present with a mass effect. Associated ipsilateral renal agenesis is a characteristic feature in more than 50% of patients as the seminal vesicles and ureteral buds originate from the mesonephric (Wolffian) duct. For management, the transrectal ultrasound provides good visualization of the seminal vesicles and the rest of the pelvic structures providing a good guidance for aspiration of the cysts. Case presentation We present a case of a seminal vesicle fluid-filled tubular lesion. The patient first complained of vague abdominal pain with lower abdominal fullness. He was clinically evaluated, and radiological evaluation was performed using different modalities, and finally, the patient took his decision to live with it without any intervention at present. Conclusions The combination of seminal vesicle cysts and ipsilateral renal agenesis, is a rare urological anomaly with an insult during the 1st trimester is to be considered as the first suspicion. Usual manifestations are caused by the seminal vesicle cysts that cause mass effect and irritation to the surroundings in the form of urinary bladder irritation and in sometimes obstruction as well as pain/discomfort in the perineum and scrotum. Epididymitis is frequently occurring as a complication. Treatment mainly consists of removing the seminal vesicle cyst/tubular lesion.http://link.springer.com/article/10.1186/s43055-020-00336-6Zinner’s syndrome case reportSeminal vesicle cystic lesionUnilateral renal agenesisEjaculatory duct obstruction
collection DOAJ
language English
format Article
sources DOAJ
author Ahmed Atef Soliman
Anwar Ali Alshukami
Walaa Hussein AlZuber
spellingShingle Ahmed Atef Soliman
Anwar Ali Alshukami
Walaa Hussein AlZuber
Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
The Egyptian Journal of Radiology and Nuclear Medicine
Zinner’s syndrome case report
Seminal vesicle cystic lesion
Unilateral renal agenesis
Ejaculatory duct obstruction
author_facet Ahmed Atef Soliman
Anwar Ali Alshukami
Walaa Hussein AlZuber
author_sort Ahmed Atef Soliman
title Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
title_short Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
title_full Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
title_fullStr Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
title_full_unstemmed Zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
title_sort zinner’s syndrome, radiological diagnosis for a rare syndrome with non-specific clinical presentation: case report
publisher SpringerOpen
series The Egyptian Journal of Radiology and Nuclear Medicine
issn 2090-4762
publishDate 2020-10-01
description Abstract Background Zinner’s syndrome is a rare congenital malformation involving the seminal vesicle that mostly shows cystic transformation. Embryogenesis of the kidney, ureter, seminal vesicle, and vas deferens can be altered if an insult occurs during the first trimester mainly between the 4th and the 13th gestational week. Cystic lesions of the seminal vesicle may present with a mass effect. Associated ipsilateral renal agenesis is a characteristic feature in more than 50% of patients as the seminal vesicles and ureteral buds originate from the mesonephric (Wolffian) duct. For management, the transrectal ultrasound provides good visualization of the seminal vesicles and the rest of the pelvic structures providing a good guidance for aspiration of the cysts. Case presentation We present a case of a seminal vesicle fluid-filled tubular lesion. The patient first complained of vague abdominal pain with lower abdominal fullness. He was clinically evaluated, and radiological evaluation was performed using different modalities, and finally, the patient took his decision to live with it without any intervention at present. Conclusions The combination of seminal vesicle cysts and ipsilateral renal agenesis, is a rare urological anomaly with an insult during the 1st trimester is to be considered as the first suspicion. Usual manifestations are caused by the seminal vesicle cysts that cause mass effect and irritation to the surroundings in the form of urinary bladder irritation and in sometimes obstruction as well as pain/discomfort in the perineum and scrotum. Epididymitis is frequently occurring as a complication. Treatment mainly consists of removing the seminal vesicle cyst/tubular lesion.
topic Zinner’s syndrome case report
Seminal vesicle cystic lesion
Unilateral renal agenesis
Ejaculatory duct obstruction
url http://link.springer.com/article/10.1186/s43055-020-00336-6
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