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zinner syndrome radiology

Zinner's Syndrome. Unable to process the form. (2)Department of Radiology, Division of Vascular and Interventional Radiology, Christian Medical College, Vellore, India. ADVERTISEMENT: Radiopaedia is free thanks to our supporters and advertisers. Zinner’s syndrome should be suspected if a male young patient presents with unilateral renal agenesis and pelvic complaints and has a supraprostatic mass on digital rectal examination. Zinner syndrome is a triad of Wolffian duct anomalies comprising unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. 3. A young male with vague lower abdominal pain underwent screening ultrasound, which showed absent left kidney. Fiaschetti V, Greco L, Giuricin V, et al. Zinner A. Ein fall von intravesikaler samenblasenzyste. The association of ipsilateral renal agenesis and cystic seminal vesicle is a rare congenital syndrome described by Zinner in 1914. This case is one of the first to be reported in the Kingdom of Saudi Arabia. Another tubular cystic structure was also seen extending from left seminal vesicle cyst into the midline posterior prostatic urethral wall - representing obstructed dilated left ejaculatory duct. Zinner syndrome diagnosed by magnetic resonance imaging and computed tomography: role of imaging to identify and evaluate the uncommon variation in development of the male genital tract. Seminal vesicle cyst with ipsilateral renal agenesis. 1. World J Nucl Med. In view of the above-mentioned clinical and radiological findings, the diagnosis of Zinner syndrome was made. Uroradiology & genital male imaging . 52 (1): e13397. The seminal vesicle cyst was seen indenting the posterolateral wall of the urinary bladder. AJR Am J Roentgenol. 11 (4): 313-317. Vernekar . … Clinical Cases Authors. Zinner syndrome refers to the triad of ipsilateral renal agenesis, seminal vesicle cysts and ejaculatory duct obstruction. All patients underwent a contrast‐enhanced computed tomography (CT) exam. CT abdomen with intravenous contrast was done for further evaluation. The mutual embryological origins of the seminal vesicle and the ureteral bud result in both anomalous genital and urinary tracts. Zinner syndrome is a triad of Wolffian duct anomalies comprising unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. It is considered to be the anomaly development in early embryogenesis affecting the distal part of Mullerian duct. Zinner syndrome is a rare variant of wolffian duct anomalies with a triad of seminal vesicle cyst, ipsilateral renal agenesis, and male fertility problems due to ejaculatory duct obstruction (EDO). A patient has a known history of right-sided renal agenesis. {"url":"/signup-modal-props.json?lang=us\u0026email="}. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle cystic dilatation, and ipsilateral ejaculatory duct obstruction. Case Presentation . 2Department of Radiology, South Warwick Hospital, Warwick, UK 3Department of Urology, South Warwick Hospital, Warwick, UK Address correspondence to: Miss Sonali Shah E-mail: sonalishah@nhs.net ABSTRACT Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle obstruction Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report: Benedikt Hergan,Franz A. Fellner,Kaveh Akbari: Radiology Case Reports. Ipsilateral seminal vesicle cyst was seen, causing prominent impression on the posterolateral wall of the urinary bladder. 2010;26 (3): 444-7. Unable to process the form. {"url":"/signup-modal-props.json?lang=us\u0026email="}. Naval-Baudin P, Carreño García E, Sanchez Marquez A, Valcárcel José J, Romero NM. Zinner’s syndrome is a congenital malformation of the seminal vesicle and ipsilateral upper urinary tract that was first discovered in 1914 [].This includes the seminal vesicle cyst, ejaculatory duct obstruction, and ipsilateral renal agenesia. The cysts are symptomatic during the 3th-4th decade of life. Zinner syndrome which was first reported in 1914 by Zinner is described as seminal vesicle cyst with ipsilateral renal agenesis . Since 1914 that Zinner reported the association between seminal vesicle cyst and ipsilateral renal agenesia , several researchers have published their experience with diagnosis and management of this rare syndrome [1–6]. Article By Ankush N.Charles J.A. Zinner’s syndrome is a congenital malformation of the seminal vesicle and ipsilateral upper urinary tract that was first discovered in 1914 [].This includes the seminal vesicle cyst, ejaculatory duct obstruction, and ipsilateral renal agenesia. (3)Department of Radiology, University of Minnesota, Minneapolis, Minnesota. Seminal vesicle cyst and ipsilateral renal agenesis. Since then fewer than 100 cases have been reported about the diagnosis and management of this rare syndrome. Case Report. This study aims to emphasise the importance of imaging in the diagnosis and treatment decision‐making in Zinner syndrome and provide a classification for seminal vesicle cysts. Zinner's syndrome is an uncommon urogenital malformation of congenital seminal vesicle cyst associated with ipsilateral renal agenesis. 4. Trans-urethral resection of ejaculatory duct cyst was advised as a definitive treatment option and close follow-up as an alternative option. Radiology Case Reports. Abstract. ... 1 Department of Radiology, Guangdong Women and Children Hospital, Guangzhou 511400, China. CT abdomen with intravenous contrast was done for further evaluation. Silveri M, Zaccara A, Colajacomo M, et al. Figure 1 Zinner syndrome is a rare Wolffian duct anomaly, comprising a triad of unilateral renal agenesis, ipsilateral ejaculatory duct obstruction, seminal vesicle cysts. Urology. A Rare Case of Zinner Syndrome . Zinner syndrome is a triad of Wolffian duct anomalies, comprising ipsilateral ejaculatory duct obstruction, seminal vesicle cysts, and unilateral renal agenesis. 3. Right kidney is normal in size, location and parenchymal density. Denes FT, Montellato NI, Lopes RN et-al. The initial approach should be medical, but invasive procedures may be the only way to solve the patient’s complaints. Absent ureter, existence of ureteral bud, absent trigone, testicular ectopia, contralateral seminal Introduction. Multicystic seminal vesicle with ipsilateral renal agenesis: two cases of Zinner syndrome. Zinner syndrome was first described by A Zinner in 1914 8. The data of six patients with Zinner syndrome in a single institution were collected. 2009;50 (4): 560-3. An abnormal ureteric bud leads to renal agenesis or dysplasia. Zhengwu Tan, Bing Li, Lan Zhang, et-al. Check for errors and try again. Scand J Urol 2017;51:81–4. Zinner syndrome diagnosed by magnetic resonance imaging and computed tomography: role of imaging to identify and evaluate the uncommon variation in development of the male genital tract. The initial approach should be medical, but invasive procedures may be the only way to solve the patient’s complaints. ADVERTISEMENT: Radiopaedia is free thanks to our supporters and advertisers. The patients are usually diagnosed in the 2nd-3rd decade of life and present with symptoms of dysuria (37%), frequency (33%), perineal pain (29%), and epididymitis (27%) . Shibani Mehra, Rajeev Ranjan and Umesh Chandra Garga, Zinner syndrome—a rare developmental anomaly of the mesonephric duct diagnosed on magnetic resonance imaging, Radiology Case Reports, 11, 4, (313), (2016). 2011;10 (1): 20-2. Indian J Urol. A young male with vague lower abdominal pain underwent screening ultrasound, which showed absent left kidney. Radiology 178 (1991): 207-211. Zinner's syndrome, first described in 1914 by Zinner, is a rare congenital malformation of the seminal vesicles and ipsilateral upper urinary tract , . Maldevelopment of the distal part of the mesonephric duct results in atresia of the ejaculatory duct (leading to obstruction and dilatation of the seminal vesicle), while an abnormality in the ureteral bud leads to renal agenesis/dysplasia 1. Zinner's syndrome, first described in 1914 by Zinner, is a rare congenital malformation of the seminal vesicles and ipsilateral upper urinary tract , . 7. Contrast-enhanced and renal excretory phase images of the abdomen show absence of left kidney in renal fossa or other abdominal ectopic sites - representing renal agenesis. (2016) Radiology case reports. Zinner syndrome is a triad of Wolffian duct anomalies comprising of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction. Seminal vesicle cysts should be differentiated from other cysts such as 4: ADVERTISEMENT: Supporters see fewer/no ads, Please Note: You can also scroll through stacks with your mouse wheel or the keyboard arrow keys. Irrespective of imaging modality, the key findings are 1: Small testis and ipsilateral ureterocele have also been reported 7 . 1. A brief review o … The cases of two patients with this syndrome are presented, one of them associated with infertility, the other with cryptorchidism and testicular pain. Classifying seminal vesicle cysts in the diagnosis and treatment of Zinner syndrome: A report of six cases and review of available literature. Key points of this syndrome: is a triad of Mullerian duct anomalies comprising of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction … Additional contributor: R. Bouguelaa, MD. Zinner syndrome: rare cause of agenesis of the kidney Abstract The trias of renal agenesis, unilateral cyst ... afdeling Radiologie, RijnstateArnhem, Arnhem, Nederland in 1914 by dr. Zinner. Zinner syndrome refers to the triad of ipsilateral renal agenesis, seminal vesicle cysts and ejaculatory duct obstruction. There is an association between congenital malformations of the seminal vesicle and the ipsilateral upper urinary tract because both the ureteral buds and the seminal vesicles originate from the mesonephric (Wolffian) duct 2,3. 6. 2. 5. Sundar R(1), Sundar G(2). Yonsei Med. 1 It is believed that an embryologic development abnormality of the Wolffian duct will induce ipsilateral renal agenesis and atresia of the ejaculatory duct. Seo IY, Kim HS, Rim JS. There was also dilatation of left ejaculatory duct, which was seen as a tubular cystic structure extending up to midline posterior prostatic urethra. Seminal vesicle cyst and ipsilateral renal agenesis. Case Type. Zinner syndrome, which was described by Zinner in 1914, has a triad of "unilateral ejaculatory duct obstruction, SV cysts and ipsilateral renal agenesis". Kuo J, Foster C, Shelton DK. Zinner’s syndrome should be suspected if a male young patient presents with unilateral renal agenesis and pelvic complaints and has a supraprostatic mass on digital rectal examination. They can be classified into anomalies of number (agenesis, fusion), canalization (cysts), and maturation (hypoplasi… This condition was first described by Zinner in 1914. Zinner syndrome Section. 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