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Persistent Mullerian Duct Syndrome with Embryonal Cell Carcinoma along with Ectopic Cross Fused Kidney [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Persistent Mullerian Duct Syndrome (PMDS) is a form of internal male pseudohermaphroditism, where there is normal development of male secondary sexual characters, along with the presence of bilateral fallopian tubes and uterus.
ARUN KUMAR BARAD   +4 more
doaj   +2 more sources

Open pyelolithotomy in incompletely duplicated kidney with contralateral crossed fused ectopia: A rare case report [PDF]

open access: yesUrology Case Reports
Crossed fused renal ectopia is a rare congenital anomaly that can lead to urinary stasis, infection, and stone formation, although its aberrant anatomy often complicates both endoscopic and percutaneous access and treatment.
Nouraldin Ibrahim Hih   +5 more
doaj   +2 more sources

Rare case of triple kidney with horseshoe fusion [PDF]

open access: yesRadiology Case Reports
Congenital anomalies of the kidney and urinary tract represent a heterogeneous group of malformations, often detected incidentally but occasionally associated with complications.
Salma El Aouadi, MD   +7 more
doaj   +2 more sources

Combined ultrasound and scintigraphic assessment of coexisting pelvic and cross-fused renal anomalies in a neonate: A case report [PDF]

open access: yesRadiology Case Reports
Cross-fused renal ectopia and pelvic kidney are individually well-documented congenital anomalies, but their concurrent occurrence is exceedingly uncommon.
Shatha J Almushayt, PhD   +1 more
doaj   +2 more sources

Acute obstructive pyelonephritis revealing a crossed non-fused renal ectopia in the early postpartum period: A case report [PDF]

open access: yesUrology Case Reports
Non-fused crossed renal ectopia (CRE) is a rare congenital anomaly where one kidney migrates contralaterally without fusion. We report a 31-year-old woman presenting nine days postpartum with febrile abdominal pain revealing a left non-fused crossed ...
Younes Houry   +7 more
doaj   +2 more sources

Crossed Fused Ectopic Kidney: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Crossed fused ectopic kidney is an unusual congenital malformation of the urinary tract. This condition is usually identified in the autopsy specimen rather than in general clinical scenario.
Rohit Bhattar   +3 more
doaj   +3 more sources

Fused Right Supernumerary Kidney: A Case Report

open access: yesJournal of Nepal Medical Association, 2019
Supernumerary kidney is a rare clinical entity with fused supernumerary kidney being even rarer. Caudally located fused right supernumerary kidney with multiple nephrolithiasis was diagnosed in a 69-years-old lady by Computed Tomography Urography.
Sagun Manandhar, Ashish Khanal
doaj   +3 more sources

Retroperitoneoscopic nephrectomy for crossed-fused ectopic kidney

open access: yesIndian Journal of Urology, 2009
A 25-year-old female presented with a history of recurrent urinary tract infection and end stage renal failure. Voiding cystourethrography revealed bilateral Grade IV vesicoureteral reflux with left to right crossed ectopia.
Pranjal Modi   +3 more
doaj   +3 more sources

Laparoscopic resection for low rectal cancer in a patient with horseshoe kidney – Technical considerations to prevent iatrogenic injuries

open access: yesJournal of Minimal Access Surgery, 2021
Horseshoe kidney (HSK) is a rare congenital malformation of the kidneys and is commonly associated with other anomalies of the renovascular and ureteropelvic systems.
B Vigneshwaran   +4 more
doaj   +1 more source

Pelviureteric junction obstruction of the ipsilateral kidney caused by hydronephrosis secondary to crossed fused renal ectopia

open access: yesIJU Case Reports, 2022
Introduction Crossed fused renal ectopia is rare and usually asymptomatic. However, it is associated with urological anomalies. Case presentation A 15‐year‐old Japanese boy was transported to our hospital with right abdominal pain and hematuria after a ...
Taiki Kato   +9 more
doaj   +1 more source

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