Results 21 to 30 of about 71,234 (261)

Fused Supernumerary Kidney with Single Pelvis and Ureter; Presenting with Stones: A Case Report and Literature Review

Research and Reports in Urology, 2021
Tekleberhan Berhe, Seid Mohammed Hassen, Fitsum Gebreegziabher Gebrehiwot, Ferid Ousman Mummed, Feysel Hassen Issack, Masresha Solomon Dino, Sena Sefera Akkasa, Getachew Adamu Zerihun, Kaleab Habtemichael Gebreselassie Urology Unit, Department of Surgery,
Berhe T, Hassen SM, Gebrehiwot FG, Mummed FO, Issack FH, Dino MS, Akkasa SS, Zerihun GA, Gebreselassie KH   +8 more
doaj  

Embolization of an angiomyolipoma in a crossed fused renal ectopia

Urology Case Reports, 2020
‏: Crossed fused ectopic kidney represents a rare congenital malformation, and development of an angiomyolipoma (AML) in a crossed fused ectopia is even rarer. There is no clear association between both entities.
Waseem Tayeb, Raghad Aldibane, Almamoon Justaniah, Hattan Badr   +3 more
doaj   +1 more source

Fused supernumerary kidney: a clinical image.

The Pan African medical journal, 2023
A partially fused left supernumerary kidney with separate collecting systems and single ureter is diagnosed by using ultrasonography and multi-phased computed tomography (CT). The CT revealed separate renal arteries supplying both kidneys on the left side.
Sushma Myadam, Revat Meshram
openaire   +3 more sources

Crossed Fused Ectopic Kidney with Stone Disease and Bifid Renal Pelvis: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Crossed fused ectopic kidney is a rare congenital anomaly wherein the kidneys are present on the same side due to fusion. It is a rare disease that may remain undiagnosed throughout life.
Vikram Satav, Ashish Gavade, Vilas Sabale, Sunil Mhaske, Shashikant Asabe   +4 more
doaj   +1 more source

Diagnosis of Rare Association of Orthotopic Multicystic Dysplasia with Crossed Fused Renal Ectopia

Case Reports in Urology, 2014
Orthotopic multicystic dysplastic kidney with crossed fused ectopia is a rare congenital anomaly. This congenital anomaly may give an appearance of a solitary kidney morphology during the initial imaging evaluation.
Linnan Tang, June Koshy, Melissa R. Spevak, Jane E. Benson, Thangamadhan Bosemani   +4 more
doaj   +1 more source

Crossed Fused Renal Ectopia showing Pelviureteric Junction Obstruction with Single Ureter and Single Renal Artery [PDF]

Journal of Clinical and Diagnostic Research, 2019
Crossed fused renal ectopia is a rare anomaly remaining asymptomatic by far and detected invariably as either incidental finding or in view of pre-existing kidney disease.
RAHUL DEV, GITANJALI KHORWAL, MOHIT TAYAL, VIBHU GOEL, UDIT CHAUHAN   +4 more
doaj   +1 more source

Triple Fused Supernumerary Kidneys with Five Pelvicalyceal Systems

Société Internationale d’Urologie Journal
We present a case of supernumerary kidney with fusion of all three kidney units with five pelvicalyceal system (bilateral bifid PCS and PCS of supernumerary kidney). This is probably the first such case reported in literature.
Naveen Kumar, Srishti Sharma, Kashif Rizwi   +2 more
doaj   +1 more source

Supernumerary kidney forming isthmus of horseshoe kidney: A rare presentation

Indian Journal of Urology, 2020
Supernumerary kidney is one of the rarest congenital anomalies of the genito-urinary tract. Around 100 cases have been reported in the literature so far. Even rare is the fusion of a supernumerary kidney. The supernumerary kidney has its own blood supply,
Anand Dilip Vakade, S R Sudin, K Sasidharan, S Jayasudha   +3 more
doaj   +1 more source

Rapid Response to Trametinib Combined With Chemotherapy for Infant BRAF‐Fused Chiasmatic Glioma

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Infants, less than 1 year, with chiasmatic gliomas (ICG) present a major therapeutic challenge due to large tumor size, decreased vision, rapid progression, and poor response to vincristine/carboplatin chemotherapy. The majority have a BRAF fusion, which may respond to downstream MEK inhibitors but response time is slow. There are no safety or
Helen Toledano, Alexander Yelak, Walid Kaadan, Shlomo Caduri, Rivka Friedland, Orli Michaeli, Gad Dotan, Osnat Konen   +7 more
wiley   +1 more source

Duplication of Inferior Vena Cava with Associated Anomalies: A Rare Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Duplication of inferior vena cava is an uncommon abnormality and is important in daily today practice for vascular surgeons, radiologist and urologist especially during retroperitoneal surgeries and treatment of thromboembolic disease.
Pramod Shaha, Ashish Garg, Kulamani Sahoo, Nupoor Kothari, Pooja Garg   +4 more
doaj   +1 more source