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Idiopathic Nodular Glomerulosclerosis in a Long-term Passive Smoker With Recently Diagnosed Hypertension: A Case Report.
J Investig Med High Impact Case Rep
March 2025
Loma Linda University Medical Center, CA, USA.
Idiopathic nodular glomerulosclerosis (ING) is mostly associated with long-standing active smoking and hypertension (HTN). Herein, we present a rare case of ING in a passive smoker with recently diagnosed uncontrolled HTN. A 60-year-old white female with Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal plasma cell disorder, Skin changes (POEMS) syndrome and newly diagnosed HTN was referred because of an elevated creatinine level.
View Article and Find Full Text PDFZinner syndrome: report of a case and whole exome sequencing.
Basic Clin Androl
March 2025
Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430074, China.
Background: Zinner syndrome is a rare congenital malformation of the male genitourinary system, characterized by a triad: seminal vesicle cyst, unilateral renal agenesis, and ipsilateral ejaculatory duct obstruction. The etiology of this uncommon disease remains largely elusive; however, genetic mutations may contribute to its development. In this report, we present a case of symptomatic Zinner syndrome that was surgically treated, alongside an investigation into the potential genetic basis of the syndrome via whole exome sequencing.
View Article and Find Full Text PDFBones, Stones, and Hematuria - Connecting the Dots.
Indian J Nephrol
June 2024
Pediatric Nephrologist, Command Hospital, Pune, Maharashtra, India.
We report a 12 yr old boy who presented with recurrent gross hematuria, polyuria and rickets with growth failure. Investigations showed bilateral renal calculi with small kidneys on ultrasonography along with hypercalciuria; hypomagnesemia and reduced kidney function. His younger sibling also had nephrocalcinosis hypomagnesemia.
View Article and Find Full Text PDFSAFETY AND EFFICACY OF ENDOVASCULAR TREATMENT FOR CONGENITAL RENAL ARTERIOVENOUS FISTULAS.
Ann Vasc Surg
March 2025
Università Cattolica del Sacro Cuore, Rome, Italy. Unit of Vascular Surgery, Fondazione Policlinico Universitario A. Gemelli I.R.C.C.S; Unit of Vascular Surgery, Fondazione Policlinico Universitario A. Gemelli I.R.C.C.S., 00168 Rome, Italy.
Introduction: Congenital renal arteriovenous fistulas (AVF) represent an uncommon and varied group of diseases, with a reported prevalence of 0.04%. Despite rare they are clinically relevant as burdened with risk of right heart failure or aneurysmal evolution with possible rupture.
View Article and Find Full Text PDFUreteric fibroepithelial polyps in children: Retrospective study and systematic review of a rare urological presentation.
J Pediatr Urol
February 2025
Queensland Children's Hospital, Paediatric Surgery, Brisbane, Queensland, Australia.
Background: Fibroepithelial polyps are rare, benign lesions of mesodermal origin that have been reported in the genitourinary, oral, auditory and respiratory systems. Ureteric fibroepithelial polyps are extremely rare, with less than 200 cases reported in children over the past 20 years. The purpose of this study is to present a retrospective study and systematic literature review of children with fibroepithelial polyps.
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