Results 41 to 50 of about 42,662 (171)
A 30-year retrospective study of rare ectopic seminal tract opening cases
Asian Journal of Andrology, 2020 Ectopic seminal tract opening is a rare congenital malformation. Until recently, there has been a lack of comprehensive reporting on the condition. The purpose of this retrospective study is to summarize the experience of diagnosis and treatment of this ...
Hong-Fei Wu +6 more
doaj +1 more source
The Prostate, Volume 82, Issue 5, Page 576-583, April 1, 2022., 2022 Abstract Background Ductal adenocarcinoma (DA) is an aggressive subtype of prostate cancer. It is most commonly seen in mixed tumors together with conventional acinar adenocarcinoma (AA). The genetic profile of DA and its clonal origin is not fully characterized.
Claes Lindh +7 more
wiley +1 more source
Giant multilocular prostatic cystadenoma in a young man: A case report from Jordan
Clinical Case Reports, Volume 10, Issue 3, March 2022., 2022 Abstract Giant Multilocular Prostatic Cystadenoma (GMPC) is one of the rare benign tumors of the prostate. This report presents a case of a young man who has been recently diagnosed with GMPC. Our report highlights the importance of timely diagnosis and treatment, considering the overlapping symptoms with other common urinary conditions.
Mohammad Kh. Alzawahreh +8 more
wiley +1 more source
Prune Belly Syndrome Associated with Interstitial 17q12 Microdeletion
Case Reports in Urology, Volume 2022, Issue 1, 2022., 2022 We report a term male neonate presenting with a “prune belly,” bilateral hydronephrosis, hydroureter, posterior urethral obstruction, and bilateral undescended testes. Analysis with the whole genome SNP microarray revealed an interstitial deletion of about 1.49 megabase (MB) at chromosome 17q12.
Surasak Puvabanditsin +7 more
wiley +1 more source
Andrologia, Volume 53, Issue 6, July 2021., 2021 Abstract We aimed to evaluate and compare the clinical diagnostic values of magnetic resonance imaging (MRI) and ultrasound in patients with intractable haematospermia. We performed a retrospective review of 23 patients with intractable haematospermia who were diagnosed with seminal vesicle haematocele and/or calculi by transurethral seminal ...
Hu Han +3 more
wiley +1 more source
Asian Journal of Andrology, 2020 This study aimed to describe endoscopic anatomy of the seminal tract and summarize our experience of transutricular seminal vesiculoscopy (TSV) guided by real-time transrectal ultrasonography (TRUS) in managing persistent hematospermia.
Xue-Sheng Wang +8 more
doaj +1 more source
Laparoscopic management of a giant prostatic utricle: A case report and review of literature [PDF]
, 1970 Prostatic utricle is a Mullerian duct remnant with an incidence of 1 %. Excision of utricle is challenging because of the close proximity of seminal vesicle, ejaculatory ducts, bladder, rectum, ureter, and nerve plexus. Here, we report the case of a
Sharma, Umesh +3 more
core +1 more source
Urology Case Reports, 2020 Duplication of the ureters with distal, supra-sphincteric, prostatic implantation is an uncommon congenital anomaly. We report a case of a 35 year-old men presenting with pelvic pain with lower urinary tract symptoms for at least 3 months duration.
Belkacem Benmohamed +5 more
doaj +1 more source
A METHOD OF TREATING THE PROSTATIC UTRICLE [PDF]
Journal of the American Medical Association, 1911 ABSTRACT Urethroscopy of the posterior urethra has been comparatively slow in developing, and not until the last few years has sufficient attention been directed to this important field. One result of this increased study has been the recognition of the important part which diseases of the verumontanum play in the production of severe and often ...
openaire +2 more sources
La Pediatria Medica e Chirurgica, 2018 Persistent Müllerian duct syndrome is a disorder of sexual development, which features a failure of involution of Müllerian structures. An enlarged prostatic utricle is a kind of Müllerian duct remnant (MDR) with a tubular shaped structure communicating ...
Mario Lima +6 more
doaj +1 more source