Results 51 to 60 of about 3,401 (187)
Duplex Renal Collecting System Lithiasis: A Case of a Challenging Management Technique
Case Reports in Urology, Volume 2025, Issue 1, 2025.Duplex renal collecting system is a relatively common congenital abnormality affecting equally both pelvicalyceal systems. Although usually it is an incidental finding, it can cause significant problems to the patients such as recurrent urinary tract infections, hydronephrosis, and lithiasis.
Ioannis Loufopoulos +3 more
wiley +1 more source
Intravesical and Unilateral Ureterocele with Ipsilateral Kidney Agenesia [PDF]
Journal of Kerman University of Medical Sciences, 2003 This is a report of a rare case of intravesical and unilateral ureterocele in a young man (25 years old) with ipsilateral kidney agenesia. He was referred to our urology clinic with frequent retention. Ultimate diagnosis made by US, IVP and CT Scan. This
A.A Ketabchi
doaj
Recurrent adult urinary tract infection secondary to unrecognized ureterocele urolithiasis
UroPrecision, Volume 2, Issue 4, Page 180-183, December 2024.Abstract Background A ureterocele is a cystic dilation of the distal ureter, most commonly presenting as a congenital abnormality that may be associated with other renal anomalies. Ureteroceles present in a variety of manifestations in both children and adults, from asymptomatic to significant flank pain with urolithiasis or recurrent urinary tract ...
Katherine Wu, James Jing
wiley +1 more source
Lower respiratory tract infections in children with congenital lung abnormalities
Pediatric Pulmonology, Volume 59, Issue 10, Page 2563-2571, October 2024.Abstract Objective We aimed to determine if the incidence of lower respiratory tract infections (LRTI) among children with asymptomatic, observationally managed congenital lung abnormalities (CLA) differed from that of symptomatic patients who underwent surgery.
Louis Dossche +5 more
wiley +1 more source
Placement of an artificial urethral sphincter in 8 male dogs with urethral diverticulum
Journal of Veterinary Internal Medicine, Volume 38, Issue 4, Page 2171-2179, July/August 2024.Abstract Background Urethral diverticulum (UD) is a poorly defined anomaly consisting of an outpouching of the urethra. Management without surgical resection is not previously reported in dogs. Hypothesis/Objectives Report the outcome of male dogs presented for urinary incontinence with UD treated with an artificial urethral sphincter (AUS).
Geoffrey Neumann +6 more
wiley +1 more source
Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome
Prenatal Diagnosis, Volume 44, Issue 6-7, Page 796-803, June 2024.Abstract Background Enlarged cavum septum pellucidum (CSP) and hypoplastic thymus are proposed extra‐cardiac fetal markers for 22q11.2 deletion syndrome. We sought to determine if they were part of the fetal phenotype of our cohort of fetuses with 22q11.2 deletion syndrome. Methods Case‐control study of fetuses evaluated from 2016 to 2022.
Kimberly B. Gaiser +10 more
wiley +1 more source
Simplified upper pole nephrectomy: initial experience
International Brazilian Journal of Urology, 2005 OBJECTIVE: To assess the results of an upper pole nephrectomy technique on 5 children. MATERIALS AND METHODS: Upper pole nephrectomy was performed on 5 children, including 4 females and 1 male. Age ranged from 3 to 6 years old.
Ubirajara Barroso Jr +5 more
doaj +1 more source
Veterinary Record Case Reports, Volume 12, Issue 2, June 2024.Abstract A 2‐year‐old, male, neutered labrador retriever with a previous diagnosis of left renal agenesis and left cryptorchidism presented for investigation of mild intermittent urinary incontinence. Abdominal ultrasound, intravenous urography and retrograde positive‐contrast urethrocystography were performed, identifying an unusual fluid‐filled ...
Lavinia Economu +3 more
wiley +1 more source
Pre‐ and postnatal findings with rare congenital anomalies of urinary bladder
Clinical Case Reports, Volume 12, Issue 4, April 2024.The authors report how 2 rare cases of congenital bladder anomalies presented prenatally and postpartum, and after surgical treatment, to help understand this rare bladder anomaly. Key Clinical Message Bladder duplication and congenital bladder diverticulum are rare anomalies.
Hui Guo +3 more
wiley +1 more source