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Int. braz. j. urol ; 43(1): 13-19, Jan.-Feb. 2017. tab, graf
Article Dans Anglais | LILACS | ID: biblio-840795

Résumé

ABSTRACT Objectives To investigate a possible causal relationship for stone formation in pelviureteric junction obstruction and to outline management options. Materials and Methods A literature search and evidence synthesis was conducted via electronic databases in the English language using the key words pelviureteric junction obstruction; urolithiasis; hyperoxaluria; laparoscopic pyeloplasty; flexible nephroscopy; percutaneous nephrolithotomy, alone or in combination. Relevant articles were analysed to extract conclusions. Results Concomitant pelviureteric junction obstruction (PUJO) and renal lithiasis has been reported only scarcely in the literature. Although PUJO has been extensively studied throughout the years, the presence of calculi in such a patient has not received equal attention and there is still doubt surrounding the pathophysiology and global management. Conclusions Metabolic risk factors appear to play an important role, enough to justify metabolic evaluation in these patients. Urinary stasis and infection are well known factors predisposing to lithiasis and contribute to some extent. The choice for treatment is not always straightforward. Management should be tailored according to degree of obstruction, renal function, patient symptoms and stone size. Simultaneous treatment is feasible with the aid of minimally invasive operative techniques and laparoscopy in particular.


Sujets)
Humains , Obstruction urétérale/chirurgie , Obstruction urétérale/complications , Dysplasie rénale multikystique/chirurgie , Dysplasie rénale multikystique/complications , Urolithiase/chirurgie , Urolithiase/complications , Hydronéphrose/congénital , Maladies métaboliques/complications , Obstruction urétérale/métabolisme , Néphrostomie percutanée/méthodes , Facteurs de risque , Laparoscopie/méthodes , Dysplasie rénale multikystique/métabolisme , Urolithiase/métabolisme , Hydronéphrose/chirurgie , Hydronéphrose/complications , Hydronéphrose/métabolisme , Pelvis rénal/chirurgie
2.
Int. braz. j. urol ; 42(3): 614-620, tab, graf
Article Dans Anglais | LILACS | ID: lil-785739

Résumé

ABSTRACT Aim Our aim is to measure asymmetric dimethyl arginine and nitric oxide levels in rats with induced unilateral acute ureteral obstruction to research the effects on the kidney. Material and Methods The study included 21 adolescent (average age 6 weeks) Sprague-Dawley male rats weighing between 240-290g divided at random into 3 groups. Group-1: Control group (n=6): underwent no procedures. Group-2: Sham group (n=6): underwent the same procedures as the experimental group without ureter and psoas muscle dissection. Group-3: Group with induced partial unilateral ureteral obstruction (n=9). All rats were sacrificed after 12 weeks. Superoxide dismutase enzyme activity and nitrite and nitrate salt levels were measured in renal tissue. Plasma nitrite-nitrate and ADMA levels were examined. Results In the experimental group histopathological changes observed included renal pelvis dilatation, flattened papillae, sclerotic glomerulus and fibrosis. In the experimental group tissue SOD and blood ADMA levels were higher than the control and sham groups (p<0.05) while tissue NO and plasma NO values were lower than in the sham and control groups (p<0.05). Conclusion Oxidative stress and disruption of NO synthesis play an important role in renal function and histopathological changes after obstructive renal disease. To prevent renal complications developing after obstructive nephropathy we believe that a new strategy may be research on reducing ADMA.


Sujets)
Animaux , Mâle , Arginine/analogues et dérivés , Obstruction urétérale/complications , Hydronéphrose/étiologie , Hydronéphrose/anatomopathologie , Monoxyde d'azote/analyse , Arginine/sang , Valeurs de référence , Superoxide dismutase/analyse , Obstruction urétérale/métabolisme , Test ELISA , Répartition aléatoire , Inclusion en paraffine , Rat Sprague-Dawley , Stress oxydatif/physiologie , Modèles animaux de maladie humaine , Hydronéphrose/métabolisme , Rein/anatomopathologie , Nitrates/analyse , Monoxyde d'azote/métabolisme
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