Zobrazeno 1 - 10
of 381
pro vyhledávání: '"Retrograde pyelography"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 10, Pp 01-03 (2024)
One in seven neonates on antenatal scan detected hydronephrosis has Pelviureteric Junction Obstruction (PUJO), making PUJO one of the most common cause of congenital urinary tract obstruction, with an incidence of one in 1000 to one in 2000 live birt
Externí odkaz:
https://doaj.org/article/bba77066f52845a1b87a21d89261932e
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 04, Pp 05-07 (2024)
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. Its rarity and anatomical abnormality make any intervention ch
Externí odkaz:
https://doaj.org/article/94ed24bd7f1645668e562c4ff555902d
Autor:
Marwa El Masri, Mehdi Mantash, Christina Abou-Malhab, Georges Aftimos, Pauline Abou-Jaoudeh, Nabil Diab
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 93, Iss , Pp 102645- (2023)
Background: Antenatal hydronephrosis can be caused by various congenital anomalies of the excretory urinary system. Common causes are isolated ureteropelvic junction obstruction and ureterovesical junction obstruction with isolated mid-ureteral steno
Externí odkaz:
https://doaj.org/article/51f9a6d2d3bb4656b5ab16ba0c44b52a
Autor:
Yuta Inoue, Yasuyuki Naitoh, Jun Ajiki, Ayako Fukui, Takeshi Yamada, Atsuko Fujihara, Kaori Yamada, Fumiya Hongo, Osamu Ukimura
Publikováno v:
IJU Case Reports, Vol 4, Iss 5, Pp 273-276 (2021)
Introduction Ureteropelvic junction obstruction is a common congenital anomaly that causes hydronephrosis but rarely accompanies ipsilateral retrocaval ureter. Case presentation A 39‐year‐old woman, who visited to our hospital complaining of wors
Externí odkaz:
https://doaj.org/article/fa371b493008488ba9e25ede18d68a87
Publikováno v:
Urology Case Reports, Vol 40, Iss , Pp 101877- (2022)
Congenital mid-ureteral strictures (CMS) are rare. Most congenital strictures occur at the ureteropelvic junction or ureterovesical junction, with mid-ureteral strictures accounting for only 4–5% of all cases of ureteral obstruction in children. Fu
Externí odkaz:
https://doaj.org/article/e147bff397194d0fbe95e489fe08cd7f
Akademický článek
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Akademický článek
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Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Congenital mid ureteric valve (MUV) stenosis is a very rare entity. Definitive preoperative diagnosis is clinically challenging, and most patients are misdiagnosed preoperatively. Intraoperative identification is therefore very important. Curative tr
Externí odkaz:
https://doaj.org/article/556256a4b7f647e2aebeba9560b9e72f
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 2, Pp PD14-PD16 (2019)
Ureteral triplication is a rare congenital anomaly of the urinary tract with around 100 reported cases in English literature. Rarer is the presence of bilateral ectopic ureter with it. Here, a case of a young female patient who presented with continu
Externí odkaz:
https://doaj.org/article/89d52343db8b45bb991a694417dfefb3