Results 1 to 10 of about 568 (139)

A case of retrocaval ureter with robot‐assisted ureteral reconstruction [PDF]

open access: yesIJU Case Reports
Introduction Retrocaval ureter is a rare congenital anomaly that causes ureteral obstruction. Because of the rarity of retrocaval ureter, only a few cases of open, laparoscopic, or robot‐assisted surgery have been reported.
Tomoaki Hakariya
exaly   +4 more sources

Robot‐assisted laparoscopic pyeloplasty for ureteropelvic junction obstruction due to aberrant blood vessel with ipsilateral retrocaval ureter [PDF]

open access: yesIJU Case Reports, 2021
Introduction Ureteropelvic junction obstruction is a common congenital anomaly that causes hydronephrosis but rarely accompanies ipsilateral retrocaval ureter.
Yuta Inoue   +8 more
doaj   +3 more sources

Rare case of carcinoma in situ originated in right retrocaval ureter successfully managed with laparoscopic procedure [PDF]

open access: yesIJU Case Reports, 2020
Introduction A retrocaval ureter is a rare congenital abnormality characterized by the persistence of the posterior subcardinal vein on the right, which causes the proximal ureter to deviate medially behind the inferior vena cava.
Yusuke Noda   +9 more
doaj   +3 more sources

Retrocaval Ureter: Report of Two Cases [PDF]

open access: yesCase Reports in Urology, 2019
Retrocaval ureter (RCU) is a rare congenital anomaly in which the ureter passes posterior to the inferior vena cava (IVC). A little over 200 cases have been reported worldwide since Hochstetter’s first report in 1893.
Henry Atawurah   +3 more
doaj   +3 more sources

Retrocaval ureter with ureteral calculus: Case report [PDF]

open access: yesUrology Case Reports, 2020
Retrocaval ureter, which also called circumcaval ureter, is a rare abnormal development where the vena cava compresses the upper segment of ureter leading to different grades of hydronephrosis.
Maher Al-Hajjaj
exaly   +4 more sources

Type II retrocaval ureter in an eleven-year-old: A case report [PDF]

open access: yesRadiology Case Reports
Retrocaval ureter is a rare congenital anomaly in which the ureter courses posterior to the inferior vena cava. It may be associated with inferior vena cava and renal anomalies. We reported an 11-year-old male presented with a history of right flank pain
Ismail Gedi Ibrahim   +2 more
exaly   +4 more sources

Retrocaval ureter associated with cryptorchidism: A case report and review of literature [PDF]

open access: yesClinical Case Reports (discontinued), 2018
We report an incidentally diagnosed retrocaval ureter in a 14‐year‐old boy, while evaluating for right‐sided hydronephrosis associated with cryptorchidism. Therefore, we suggest that any significant right‐sided hydronephrosis associated with cryptorchidism may require investigations to exclude this rare anomaly.
Umesh Jayarajah
exaly   +3 more sources

A missed diagnosis of retrocaval ureter; case report and review of the literature [PDF]

open access: yesUrology Case Reports, 2023
The retrocaval ureter is an uncommon congenital anomaly due to an abnormal development of the inferior vena cava. Our case describes an 8 year-old boy who was referred to our center as a case of ureteropelvic junction obstruction with persistent ...
Omar Abduldaem   +3 more
doaj   +2 more sources

Retrocaval ureter: A case report and review of the literature [PDF]

open access: yesUrology Case Reports, 2021
Retrocaval ureter is a rare malformation. We report a case of right retrocaval ureter of type 1. The usual clinical manifestation being lumbar pain due to obstruction of the upper urinary tract, asymptomatic forms can also be encountered.
Y. Fadil   +4 more
doaj   +2 more sources

Retrocaval ureter: a case report and review of the literature [PDF]

open access: yesJournal of Medical Case Reports
Background The retrocaval ureter is a rare congenital anomaly resulting from abnormal development of the inferior vena cava. The obstruction is usually at the retrocaval segment of the ureter, as it lies between the inferior vena cava and the body of the
Isaack Mlatie Maro   +7 more
doaj   +2 more sources

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