Results 31 to 40 of about 230,368 (279)
Radiology Case Reports, 2017 Seminal vesicle cysts are a very rare condition and its often associated with ipsilateral renal agenesis. The diagnosis of seminal vesicle cysts may be delayed or missed because of the non-specific symptoms of this condition. This article reports a triad
V. Fiaschetti, MD, PhD +7 more
doaj +1 more source
… And if this was a Zinner's syndrome?
Journal of Pediatric Surgery Case Reports, 2014 A two year-old male was seen to our Emergency Department for acute abdominal pain, urinary retention and worsening constipation. A first level diagnostic imaging showed a pelvic cystic mass between bladder and rectum. Left kidney was absent.
Massimiliano Silveri +5 more
doaj +1 more source
Zinner Syndrome with Ectopic Ureter Emptying into Seminal Vesicle
Case Reports in Urology, 2021 A 66-year-old male patient in follow-up in the urology department for a non-muscle-invasive bladder cancer was detected by ultrasound to have absence of the left kidney and a cystic, multilobed image at the location of the seminal vesicle.
M. Hevia Palacios +4 more
doaj +1 more source
A Case of Seminal Vesicle Cyst Incidentally Diagnosed during Rupture of Abdominal Subcutaneous Abscess [PDF]
, 2018 Seminal vesicle cyst is a rare disease and is often asymptomatic. We present a case of huge seminal vesicle cyst connected to the abdominal wall and observed as a subcutaneous abscess. An 89-year-old man presented with asymptomatic spontaneous rupture of
山田, 祐也 +5 more
core +1 more source
Zinner's syndrome: clinical case of a rare pathology
Вестник урологии, 2023 Zinner’s syndrome is a rare congenital urogenital anomaly characterised by the triad of seminal vesicle cyst, ipsilateral renal aplasia, and seminal duct obstruction.
D. A. Dobroserdov +3 more
doaj +1 more source
Microbiome‐blood–brain barrier interactions in aging — mechanisms and therapeutic potential
FEBS Letters, EarlyView.Aging reshapes the gut microbiome (↓SCFA‐producing commensals; ↑pro‐inflammatory outputs), shifting circulating metabolites (↓SCFAs; ↑LPS, ↑TMAO, ↑PAA) that act at the BBB to increase nonspecific transcytosis, alter transport, and promote astrocyte reactivity, heightening brain vulnerability.
Daniel Cuervo‐Zanatta +3 more
wiley +1 more source
BMC UrologyBackground Zinner syndrome (ZS) is a congenital malformation characterized by a triad of mesonephric (Wolffian) duct dysplasia, first identified by Zinner in 1914.
Guixing Tang +6 more
doaj +1 more source
Liver organoids: modelling complexity in homeostasis and disease
FEBS Letters, EarlyView.Studying liver in vitro has been challenging because simple 2D cell cultures fail to capture liver's cellular and architectural complexity. To bridge this gap, scientists increasingly use organoids, 3D liver models which better mimic liver composition and function. This review examines recent advances in liver organoid complexity and realism, discusses
Anna M. Dowbaj, Meritxell Huch
wiley +1 more source
Zinner’s Syndrome: A Rare Diagnosis of Dysuria Based on Imaging
Case Reports in Urology, 2020 Zinner’s syndrome is a rare congenital malformation of the seminal vesicle and ipsilateral upper urinary tract, due to developmental arrest in early embryogenesis of the Müllerian duct.
Ahmed Ibrahimi +7 more
doaj +1 more source
A case of seminal vesicle cyst associated with ipsilateral renal dysplasia and ectopic ureter opening into seminal vesicle [PDF]
, 1983 A case of seminal vesicle cyst associated with ipsilateral renal dysplasia and ectopic ureter opening into seminal vesicle was experienced recently in our clinic. The case was a 14-year-old boy with the chief complaint of macrohematuria.
大川, 順正 +5 more
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