scholarly journals Ejaculatory duct reflux revealed by chronic scrotal swelling in an adult

2022 ◽  
pp. 101992
Author(s):  
Selim Zaghbib ◽  
Marouene Chakroun ◽  
Hamza Boussaffa ◽  
Ahmed Saadi ◽  
Haroun Ayed ◽  
...  
Keyword(s):  
Ejaculatory Duct ◽  
Scrotal Swelling

Unusual cause of scrotal swelling

Pathology ◽  
2003 ◽  
Vol 35 (2) ◽  
pp. 166-167
Author(s):  
Hwei Yee Lee ◽  
Khoon Leong Chuah ◽  
Puay Hoon Tan
Keyword(s):  
Scrotal Swelling

scholarly journals Functional testicular torsion secondary to an incarcerated inguinal hernia in a 4-month old: complete recovery at 18-hours

2021 ◽  
Vol 2021 (2) ◽  
Author(s):  
Gregory M Taylor ◽  
Christian C Strachan
Keyword(s):  
Inguinal Hernia ◽  
Testicular Torsion ◽  
Pediatric Patients ◽  
Complete Recovery ◽  
Cord Compression ◽  
Acute Scrotum ◽  
Indirect Inguinal Hernia ◽  
Incarcerated Inguinal Hernia ◽  
Scrotal Swelling ◽  
Urological Emergencies

Abstract One of the most common urological emergencies encountered in pediatric patients in the emergency department (ED) is the acute scrotum. We present the case of a 4-month-old male that presented to our community ED with scrotal swelling and vomiting of 16-hours duration. He was diagnosed with a functional testicular torsion from an incarcerated inguinal hernia, transferred to a hospital with pediatric urological capabilities and was taken to the operating room ~2 hours later. His hospital course was unremarkable, and he was discharged on day 3, having made a full recovery without any loss of bowel or testicle. There have only been a handful of cases in the literature of a pediatric patient presenting with a functional testicular torsion as a result of spermatic cord compression from an indirect inguinal hernia, with no reported cases of complete salvage at nearly 18 hours since symptom onset.

Ejaculatory duct obstruction in subfertile males: analysis of 87 patients

1991 ◽  
Vol 56 (4) ◽  
pp. 725-730 ◽  
Author(s):  
John P. Pryor ◽  
William F. Hendry
Keyword(s):  
Ejaculatory Duct ◽  
Duct Obstruction ◽  
Ejaculatory Duct Obstruction

A wide spectrum of rare clinical variants of Zinner syndrome

2021 ◽  
Vol 14 (1) ◽  
pp. e239254
Author(s):  
Harkirat Singh Talwar ◽  
Ankur Mittal ◽  
Tushar Aditya Narain ◽  
Vikas Kumar Panwar
Keyword(s):  
Congenital Malformations ◽  
Renal Agenesis ◽  
Wide Spectrum ◽  
Ejaculatory Duct ◽  
Seminal Vesicles ◽  
Duct Obstruction ◽  
Cyst Excision ◽  
Maintenance Haemodialysis ◽  
Clinical Variants ◽  
Ejaculatory Duct Obstruction

Congenital malformations of the seminal vesicles (SVs) are rare and are associated with abnormalities of the ipsilateral urinary tracts as embryologically both the ureteral buds and SVs arise from the mesonephric ducts. The triad of SV cysts, ipsilateral renal agenesis and ejaculatory duct obstruction is known as the Zinner syndrome. We, herein, present three very rare presentations of Zinner syndrome. Case 1 presented with haematuria, and was found to have a large SV cyst with stones and underwent a robotic cyst excision. Case 2 presented with primary infertility, and was found to have a variant of Zinner syndrome. Case 3 was a known case of chronic kidney disease on maintenance haemodialysis who presented with fever and oliguria. He was found to have Zinner syndrome and underwent aspiration of SV abscess. To the best of our knowledge, such varying presentations of Zinner syndrome have been rarely reported thus far.

Renal lobar dysmorphism: a potential mimic of renal malignancy

2021 ◽  
Vol 14 (2) ◽  
pp. e237096
Author(s):  
Derek Barry Hennessey ◽  
Adrian B Brady ◽  
Rhona Dempsey ◽  
Kenneth Patterson
Keyword(s):  
Normal Tissue ◽  
Renal Mass ◽  
Intravenous Urography ◽  
Renal Ultrasound ◽  
Apparent Mass ◽  
Radiological Imaging ◽  
Radiological Findings ◽  
Anatomical Variant ◽  
Scrotal Swelling

A renal pseudotumour is any apparent renal mass that simulates a tumour on radiological imaging but is composed of normal tissue. Renal pseudotumours may be inflammatory, vascular, postsurgical or congenital. We report a case of renal lobar dysmorphism (RLD) of the kidney, a congenital renal pseudotumour. A 45-year-old man presented with scrotal swelling. Testicular ultrasound showed an epididymal cyst. Renal ultrasound showed a right solid renal apparent mass of 2.4 cm in diameter. Triphasic renal CT showed this was consistent with RLD. Intravenous urography confirmed a central calyx within the dysmorphic lobe. RLD is a rare congenital normal anatomical variant, which can appear as a renal pseudotumour. No further investigation or intervention is necessary. We present the radiological findings of RLD and review the literature.

Memoirs: On the Development of the Male Genitalia and the Efferent Genital Ducts in Lepidoptera

1933 ◽  
Vol s2-76 (301) ◽  
pp. 35-61
Author(s):  
DEV RAJ MEHTA
Keyword(s):  
Male Genitalia ◽  
Abdominal Segment ◽  
Larval Instar ◽  
Ejaculatory Duct ◽  
External Genitalia ◽  
Reproductive Organs ◽  
Proximal Portion ◽  
Genital System ◽  
Larval Life ◽  
Accessory Glands

A general account of the internal reproductive organs and the external genitalia and their development is given. The ‘penis lobes’ develop earlier than the ‘valvae lobes’, and independently of them. The tegumen is the modified ninth tergite. The tenth segment is visibly distinguished into a tergal and sternal part in the pupal stages, and the anal tube passes between the two sclerites. The uncus and the gnathos are dorsal and ventral processes respectively of the tenth segment. The anellus lobes develop as lateral processes of the ninth sternite on either side of the penis. The vasa deferentia during larval life do not extend beyond the eighth abdominal segment and lie in a latero-ventral position. They meet the extensions from the ectodermal ‘ductus ejaculatorius duplex’ during the last larval stadium. From the earliest caterpillar stage there exists a pair of ectodermal ducts formed by the differentiation of the epidermis on the ninth sternite. Towards the end of larval life they divide by constriction to form the accessory glands and the ‘ductus ejaculatory duplex’. At this stage they extend on either side to meet the vasa deferentia. The vesiculae seminales develop by distension from the region of junction between the vasa deferentia and the proximal portion of the ejaculatory duct. The ‘ductus ejaculatorius simplex’ arises as an ectodermal invagination between the pair of ‘penis lobes’ during the final larval instar. It is established that, with the exception of the vasa deferentia, all the remaining elements in the efferent genital system are derived from the ectoderm.

Zinner Syndrome with Ectopic Ureter Remnant

2021 ◽  
Vol 17 ◽  
Author(s):  
Ara Ko ◽  
Sung Bin Park ◽  
Hyun Jeong Park ◽  
Eun Sun Lee
Keyword(s):  
Seminal Vesicle ◽  
Ejaculatory Duct ◽  
Outlet Obstruction ◽  
Ectopic Ureter ◽  
Cystic Dilatation ◽  
Unilateral Renal Agenesis ◽  
Rare Congenital Abnormality ◽  
Mesonephric Duct ◽  
Clinical Triad ◽  
Ejaculatory Duct Obstruction

: Zinner syndrome is a rare congenital abnormality defined by a clinical triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction. Most patients are asymptomatic, but if the cystic dilatation of the seminal vesicle becomes significant, it can result in urinary symptoms such as dysuria and urinary retention. This rare developmental anomaly related to the mesonephric duct can also present with other abnormalities. Here, we report our experience of Zinner syndrome with bladder outlet obstruction and an ectopic ureter remnant.

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