Results 21 to 30 of about 173,669 (168)

Laparoscopic removal of congenital seminal vesicle cyst in a preadolescent male: A unique case report

Journal of the Scientific Society, 2021
Zinner syndrome refers to the triad of ipsilateral renal agenesis, seminal vesicle cysts, and ejaculatory duct obstruction. Ipsilateral renal agenesis may be associated with seminal vesicle cysts in 70% of cases, but a remnant ureteral bud has been shown
G Ajay Kumar, M N Reddy, B S R. Prasad Babu, A Lava Kumar, A Sindhuri   +4 more
doaj   +1 more source

Ejaculatory Duct Obstruction in the Setting of an Ectopic Ureter

Sexual Medicine, 2020
Introduction: A 17-year-old man was referred to a tertiary care urologist for hematuria, hematospermia, and testalgia. The patient had a history of right-sided renal dysgenesis at birth.
Joseph Shawn Smith, MD, William Patrick Springhart, MD   +1 more
doaj   +1 more source

Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract

Urology Case Reports, 2021
Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct ...
Ahmed M. Almuhanna, Shaheed Alsuhaibani, Razan Almesned, Ashraf Almatar, Hamed Alali   +4 more
doaj   +1 more source

Zinner syndrome – a rare radiological diagnosis in a young male presenting with recurrent dysuria

Journal of Society of Surgeons of Nepal, 2021
Zinner syndrome is a rare congenital abnormality of the mesonephric (Wolffian) duct consisting of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction.
Dinesh Chataut, Surendra Rayamajhi, Sundar Suwal, Ajit Thapa   +3 more
doaj   +3 more sources

Challenging clinical presentation of Zinner syndrome

Radiology Case Reports, 2023
Zinner syndrome is a rare congenital malformation of the mesonephric duct comprising of seminal vesicle cyst, ipsilateral renal agenesis, and ejaculatory duct obstruction.
Fatos Sada, MD, PhD, Elton Cekaj, MD, Blerina, Saraci, MD, Ormira Shazi, MD, Abdallah Al-Madani, MD, Sepideh Jahanian, MD, Shamsun Nahar, MBBS, Juna Musa, MD, MSc, Keti Mamillo, MD, Dijon Musliu, MD, Murtaza Ahadi, MBBS, Florim Leniqi, BSc, Tamanna Agarwal, MD, Fjolla Hyseni, MD, PhD candidate, Valon Vokshi, MD, Adam Benjamin Fink, MD, FNU Deepali, MBBS, Jeton Shatri, MD, PhD, Sadi Bexheti, MD, PhD   +18 more
doaj   +1 more source

Thyroglossal Duct Cyst With Endolaryngeal Extension [PDF]

, 2014
Thyroglossal duct cyst (TDC) arises from the remnant thyroglossal duct tract as a cystic expansion. Patients most commonly present with a palpable cystic midline neck mass or discharge from a cervical sinus opening. TDC is the most common congenital head
Taner Kemal Erdağ, Mustafa Aslıer, Ahmet Ömer İkiz   +2 more
core   +1 more source

Zinner syndrome with papillary neoplasm: A rare case report

Journal of Indian Association of Pediatric Surgeons, 2022
One of the uncommon urogenital malformations in males, which presents late in the second or third decades of life, is the congenital malformation of the seminal vesicle. Zinner syndrome is a rare condition comprising a triad of unilateral renal agenesis,
Jaskiran S Randhawa, R Shankaran, R Nagamahendran, Manoj Arun Upadhye, H Deepak   +4 more
doaj   +1 more source

Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report

Radiology Case Reports, 2020
A triad of seminal vesical cyst, ipsilateral renal agenesis and ipsilateral ejaculatory duct obstruction is known as Zinner Syndrome. First described in 1914, only about 200 cases have been reported in literature.
Benedikt Hergan, MD, Franz A. Fellner, MD, Kaveh Akbari, MD   +2 more
doaj   +1 more source

Thyroglossal Duct Cyst in a 3-Month-Old Infant: A Rare Case [PDF]

, 2016
Thyroglossal duct cyst (TGDC) is the most common congenital midline neck mass in children. It usually becomes symptomatic following a respiratory tract infection and is usually diagnosed at 5 years of age.
Ayşe Çeçen, Esra Kavaz, Sinan Atmaca
core   +1 more source

Symptomatic Müllerian Duct Cyst in a Male Adult: A Rare Case Report [PDF]

, 2017
Background: Müllerian duct cyst is an uncommon congenital anomaly. It is usually small and asymptomatic. A rare case of this entity with symptoms of ejaculatory duct obstruction such as hematospermia and secondary infertility is presented here.Case ...
Shabaninia, Shahram, Yahyazadeh, Seyed Reza   +1 more
core   +1 more source