Relevant bibliographies by topics / Uropatia malformativa

Academic literature on the topic 'Uropatia malformativa'

Author: Grafiati
Published: 11 March 2023

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Journal articles on the topic "Uropatia malformativa"

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Giovannelli, G. "Conferenze.: Uropatie Malformative." Urologia Journal 58, no. 2 (April 1991): 200–206. http://dx.doi.org/10.1177/039156039105800210.

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Hong, Lih En, Chrismin Tan, and Jordan Li. "Obstructive Uropathy Secondary to Uretero-inguinal Hernia." Journal of Clinical Imaging Science 5 (June 29, 2015): 33. http://dx.doi.org/10.4103/2156-7514.159448.

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Uretero-inguinal hernia in patients with native kidneys is rare. We report a case of an 84-year-old man who was diagnosed with obstructive uropathy secondary to uretero-inguinal hernia, with no past history of herniorrhaphy or congenital genitourinary malformation. Uretero-inguinal hernias are predominantly indirect inguinal hernias and may be paraperitoneal or extraperitoneal. Computed tomography (CT) is a non-invasive diagnostic tool for uretero-inguinal hernia. Herniorrhaphy is indicated in all cases of uretero-inguinal hernia to prevent obstructive uropathy.
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Virgilio, Robson Cristian, Fernanda Monteiro Orellana, Luiz Felipe De Melo Pereira Leitão, Tiago Granucci Guirro, Rafael Freitas de Andrade Neri, Pablo Leonardo Traete, Pedro Ivo Ravizzini, and Luis Gustavo Morato de Toledo. "Tratamento laparoscópico de cálculo ureteral em ureter retrocava / Laparoscopic treatment of ureteral stone in retrocaval ureter." Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo 66, no. 1u (May 27, 2021): 1. http://dx.doi.org/10.26432/1809-3019.2021.66.014.

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Introdução: O ureter retrocava é uma malformação congênita rara que pode ser causa de uropatia obstrutiva com sintomas inespecíficos como dor lombar e complicações como ureterolitíase e pielonefrite, que normalmente aparecem entre a terceira e a quarta décadas de vida, e exige tratamento cirúrgico na maior parte dos casos. Objetivo: Apresentar um caso de ureter retrocava associado a ureterolitíase e uma revisão da literatura a respeito das técnicas cirúrgicas para sua correção. Relato de caso: Os autores apresentam um caso de ureterolitíase e ureter retrocava, diagnosticado por tomografia computadorizada, em um paciente masculino de 43 anos com dor lombar direita, corrigido através de técnica laparoscópica transperitoneal. Conclusão: A correção cirúrgica laparoscópica do ureter retrocava tem se mostrado benéfica em diversos aspectos quando comparada ao acesso aberto e uma abordagem que ainda não havia sido publicada é a correção do ureter retrocava associado a ureterolitíase num mesmo tempo cirúrgico. Palavras chave: Ureter retrocava, Hidronefrose, Ureterolitíase, Anomalia urogenital, Laparoscopia ABSTRACT:Introduction: The retrocaval ureter is a rare congenital malformation which may cause obstructive uropathy with nonspecific symptoms such as low back pain and complications as ureterolithiasis and pyelonephritis, which usually appear between the third and fourth decades of life, and requires surgical treatment in most cases. Objective: To present a case of ureterolithiasis and retrocaval ureter and a review of literature, regarding the different types of access for his surgery. Case Report: The authors present a case of ureterolithiasis and retrocaval ureter diagnosed by computed tomography in a 43-year-old male patient with right lower back pain, corrected using a transperitoneal laparoscopic technique. Conclusion: Laparoscopic surgical correction of the retrocaval ureter has shown to be beneficial in several aspects when compared to open access, and one that has not been previously reported is the one-step resolution of the association with ureterolithiasis.Keywords: Retrocaval ureter, Hydronephrosis, Ureterothiasis, Urogenital abnormalities, Laparoscopy
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Costa, Guilherme Henrique Freire, Vitor Doria Ricardo, Jean Lucas Benatti, Juliana Lucena Queiroz, Danilo Gagliardi, José Carlos Esteves Veiga, and Celso De Castro Pochini. "Exteriorização de material cirúrgico em luz esofageana / Exteriorization of surgical material in esophagus lumen." Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo 66, no. 1u (May 27, 2021): 1. http://dx.doi.org/10.26432/1809-3019.2021.66.013.

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Introdução: O ureter retrocava é uma malformação congênita rara que pode ser causa de uropatia obstrutiva com sintomas inespecíficos como dor lombar e complicações como ureterolitíase e pielonefrite, que normalmente aparecem entre a terceira e a quarta décadas de vida, e exige tratamento cirúrgico na maior parte dos casos. Objetivo: Apresentar um caso de ureter retrocava associado a ureterolitíase e uma revisão da literatura a respeito das técnicas cirúrgicas para sua correção. Relato de caso: Os autores apresentam um caso de ureterolitíase e ureter retrocava, diagnosticado por tomografia computadorizada, em um paciente masculino de 43 anos com dor lombar direita, corrigido através de técnica laparoscópica transperitoneal. Conclusão: A correção cirúrgica laparoscópica do ureter retrocava tem se mostrado benéfica em diversos aspectos quando comparada ao acesso aberto e uma abordagem que ainda não havia sido publicada é a correção do ureter retrocava associado a ureterolitíase num mesmo tempo cirúrgico.Palavras chave: Ureter retrocava, Hidronefrose, Ureterolitíase, Anomalia urogenital, LaparoscopiaABSTRACTIntroduction: The retrocaval ureter is a rare congenital malformation which may cause obstructive uropathy with nonspecific symptoms such as low back pain and complications as ureterolithiasis and pyelonephritis, which usually appear between the third and fourth decades of life, and requires surgical treatment in most cases. Objective: To present a case of ureterolithiasis and retrocaval ureter and a review of literature, regarding the different types of access for his surgery. Case Report: The authors present a case of ureterolithiasis and retrocaval ureter diagnosed by computed tomography in a 43-year-old male patient with right lower back pain, corrected using a transperitoneal laparoscopic technique. Conclusion: Laparoscopic surgical correction of the retrocaval ureter has shown to be beneficial in several aspects when compared to open access, and one that has not been previously reported is the one-step resolution of the association with ureterolithiasis.Keywords: Retrocaval ureter, Hydronephrosis, Ureterothiasis, Urogenital abnormalities, Laparoscopy
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Inugala, Anusiri. "Neurovesical dysfunction in anorectal malformation." International Surgery Journal 7, no. 12 (November 27, 2020): 4039. http://dx.doi.org/10.18203/2349-2902.isj20205354.

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Background: Anorectal malformations are congenital anomalies characterized by the absence of a normally formed anus. Obstructive uropathy, vesicoureteral reflux neurovesical dysfunction are the leading causes of mortality and morbidity in ARM. Early diagnosis and treatment of NVD prevents renal parenchymal damage.Surgical interventions for the correction of anorectal malformation may also lead to the development of NVD. The incidence of urologic and spinal anomalies associated with ARM and the relationship between the anorectal malformations, spinal abnormalities and voiding dysfunction was studied by means of MRI spine and urodynamic studies. Methods: A prospective, observational study was done over a period of 2 years. All patients with ARM underwent MRI of the spine, ultrasound of abdomen, micturating cystourethrogram and urodynamic study.Results: Forty two patients were included in this study. Out of the 42 patients 17 (40.5%) were female and 25 (59.5%) were male. The ages of the patients ranged from 4 months to 14 years with an average of 32.9 months. 5 patients (12%) had complaints pertaining to neurovesical dysfunction. MRI of the spine revealed abnormalities in 10 patients (23.8%). Urodynamic study was abnormal in 8 patients (19%). Therefore a total of 8 patients (19%) had neurovesical dysfunction in the present study. This included 3 female patients with cloaca and 5 male patients with high anorectal malformations.Conclusions: Neurovesical dysfunction is frequently seen in patients with anorectal malformations. NVD may be due to the spinal abnormalities or due to iatrogenic injuries to the bladder innervations during surgical reconstruction.
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Ahoui, Séraphin, Gerard Kpanidja, Alphonse Noudamadjo, Falilatou Agbeille, Hermione Nelly Djima, Ahmed Adegbola, Aristide Dah, Julien Didier Adedemy, and Joseph Agossou. "Epidemiological, Clinical, and Diagnostic Aspects of Urinary Tract Infection in Newborns at the Departmental Teaching Hospital of Borgou-Alibori (DTH-B/A) in Benin." Journal of Renal and Hepatic Disorders 6, no. 1 (April 26, 2022): 41–47. http://dx.doi.org/10.15586/jrenhep.v6i1.127.

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To study epidemiological and diagnostic aspects of urinary tract infection (UTI) in newborns at the Departmental Teaching Hospital of Borgou-Alibori (DTH-B/A). This was a cross-sectional study conducted from April 1, 2019 to September 30, 2019 and concerned all newborns admitted to the neonatal unit of DTH-B/A. According to the National Agency for Health Accreditation and Evaluation (NAHAE)recommendations of 2002, all symptomatic newborns who did not have a visible malformation outside the genitourinary system and whose parents gave their consent were included in the study. The census was exhaustive despite the calculated minimum size of 109 newborns. Urine sedimentation and cytobacteriological examination of urine samples, taken in adhesive bags after local disinfection, demonstrated presence of pathogenic microbes. Sensitivity of detected microbes was studied to different antibiotics. Interpretive reading of antibiograms was established according to the Standards of the French Society of Microbiology (FEMS), edition 2012. If UTI was confirmed, an abdominopelvic ultrasound was performed in search for a malformative uropathy as a contributing factor in newborns. A standardized survey was developed for data collection. The data entered were analyzed using the Epi info software, version 3.5.4. In all, 124 newborns were included in the study. UTI accounted for 8.06% of all neonatal infections and 2.15% of admissions. The average age of onset was 7.8 days, with a gender ratio of 1:1. The main clinical manifestations were jaundice and respiratory distress. Microbes involved were Staphylococcus aureus (6/10), Escherichia coli (2/10), and Klebsiella oxytoca (2/10). The resistance of microbes to antibiotics was generally high. No abnormalities were revealed in the ultrasound. Although neonatal UTI is not a rare infection, bacterial resistance is of concern.
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Kone, KalyanaRam. "Arteriovenous malformation causing obstructive uropathy: A different dimension to ovarian vein syndrome." Indian Journal of Urology 30, no. 4 (2014): 448. http://dx.doi.org/10.4103/0970-1591.139580.

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Batouche, D. D., L. Sadaoui, M. Sadaoui, and Z. Mentouri-Chenntouf. "Uropathie malformative et son évolution vers l’insuffisance rénale chronique chez l’enfant au CHU d’Oran." Néphrologie & Thérapeutique 9, no. 5 (September 2013): 287. http://dx.doi.org/10.1016/j.nephro.2013.07.209.

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Aurore Albane Essomba, Kamsu Zicfried, Jeannette Euranie Kouam, Marguerite Edongue, Sophie Nzotsa, Michèle Natacha Engama, Daniel Armand Kago Tague, and Evelyn Mah. "OEIS complex: A case report and literature review of a rare polymalformative syndrome." World Journal of Advanced Research and Reviews 14, no. 3 (June 30, 2022): 284–90. http://dx.doi.org/10.30574/wjarr.2022.14.3.0551.

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Introduction: The OEIS complex or syndrome is the most severe form of the exstrophy-epispadias complex and is characterized by the existence of an omphalocele, bladder exstrophy, anal imperforation and spina bifida. We report an atypical case of OEIS complex associated with further birth defects admitted to our department. The diagnostic and therapeutic approach to the complex congenital malformations involved are highlighted, as well as difficulties encountered in a limited resource setting. Case Report: This was a neonate referred for the management of a congenital malformation on the first day of life. The baby was born vaginally at 35 weeks of gestation with a birth weight of 2000 g and significant major risk factors for neonatal sepsis. Two antenatal ultrasounds had revealed fetal uropathy. On admission, the clinical exam revealed: a type 1 omphalocele, an anorectal malformation with a recto-urinary fistula and a covered lumbosacral dysraphism. Paraclinical examinations revealed an associated cardiac anomaly. The karyotype analysis was not done due to lack of financial means. Supportive care was given and the neonate underwent surgical reconstruction of birth defects on day 20. Conclusion: The OEIS complex is a rare morbid congenital polymalformative syndrome in neonates. Patients require keen diagnostic enquiry and immediate postnatal multidisciplinary management, with long-term follow-up.
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Mulenga, Cuthbert, Dr Osward Bwanga, and Dr Thabo A. Moloi. "Incidental Finding of Posterior Urethral Valve during Routine Antenatal Ultrasound: Diagnostic Imaging Case Report in Botswana." EAS Journal of Radiology and Imaging Technology 4, no. 2 (April 30, 2022): 17–22. http://dx.doi.org/10.36349/easjrit.2022.v04i02.003.

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Medical ultrasound is a particularly useful imaging method used in the diagnosis of urinary fetal anomalies. One such fetal anomaly is the posterior urethral valve (PUV), which is a congenital malformation of the male urethra occurring early in gestation life. PUV is a common cause of obstructive uropathy in males and fetal death during pregnancy. We report from a medical imaging perspective on a rare and high-risk case of a PUV detected during routine antenatal ultrasound imaging in Botswana. The first scan performed at 16 weeks of gestation age was unremarkable. However, subsequent antenatal ultrasound scans at and after 20 weeks demonstrated bilateral hydronephrosis, distended ureters, and a urinary bladder which gradually increased with the gestation age. There was also a corresponding reduction in amniotic fluid and fetal movements. As a result of these complications, the pregnancy was classified as a “high-risk.” At 30 weeks, spontaneous labour occurred, and a fresh still birth male fetus was delivered.
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Dissertations / Theses on the topic "Uropatia malformativa"

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Centi, Sonia. "Identificazione di pattern di espressione genica della displasia renale associata ad uropatia malformativa." Doctoral thesis, Università degli studi di Padova, 2008. http://hdl.handle.net/11577/3425156.

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Normal kidney and urinary tract development is a complex process, regulated by a strict space-time-corrected sequential activation of a cascade of genes encoding transcription factors, growth factors, cell death/proliferation factors and adhesion molecules. An alteration disrupting this sequential gene expression may cause a defective ureteric bud-to-metanephric mesenchyme cross-talk that results in a renal and urinary tract developmental abnormality (congenital anomalies of kidney and urinary tract - CAKUT). Phenotype severity depends on the stage of nephrogenesis in which the alteration of the developmental program occurs, thus renal dysplasia is the most severe manifestation. However, little is known about CAKUT pathogenesis. The recent advent of microarray technology provided an unique tool to identify genes potentially involved in the pathogenesis of several diseases. During the first stage of this research, we applied the microarray technique to study gene expression profiles of primary renal cell cultures, using an array composed by 21329 oligonucleotides. The aim was to identify potential biomarkers of renal dysplasia. Four genes seemed to be more interesting (UPK1B, SOX11, SPRY1, MMP2). We analysed the expression of these four genes using Real Time PCR on RNA extracted from renal tissue samples of 10 patients with a histological picture of renal dysplasia and 10 with histologically normal renal tissue. Mutation analysis of SPRY1 gene, whose murine homologue is hugely involved in the regulation of GDNF growth factor's expression during ureteric branching, was carried out on 27 patients with renal duplicity. Mutation analysis identified 2 new genomic variants - whose frequency was analysed in a control population - that may be "genomic variants involved in splicing" (SpaGVs). Our research results allow to hypothesize that SPRY1 gene may be involved in the pathogenesis of kidney and urinary tract developmental diseases.
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Deghaye, Michel. "Uropathies malformatives de l'enfant : revue generale des obstructions du haut appareil urinaire." Lille 2, 1989. http://www.theses.fr/1989LIL2M159.

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POTARD, TANGUY. "Uropathies malformatives de l'enfant : aspects cliniques, paracliniques, therapeutiques et evolutifs : a propos de 205 observations recueillies sur une periode de 14 ans dans un service de pediatrie generale." Amiens, 1988. http://www.theses.fr/1988AMIEM017.

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BARRAL, VANDERSTICHELE SOPHIE. "Diagnostic antenatal des malformations uro-renales : conduite a tenir ; a propos de 147 observations." Lille 2, 1994. http://www.theses.fr/1994LIL2M344.

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PROUDHON, JEAN-FRANCOIS. "Diagnostic prenatal et prise en charge obstetricale des uropathies malformatives : une experience de 104 cas en 10 ans." Rennes 1, 1992. http://www.theses.fr/1992REN1M105.

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LEONARD, JOELLE. "Apport de l'echographie dans le depistage antenatal des uropathies malformatives." Nice, 1988. http://www.theses.fr/1988NICE6023.

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BENELLI, MARTINE. "Evaluation de la fonction renale chez les foetus atteints d'uropathies malformatives bilaterales : etude preliminaire a propos de 8 cas." Toulouse 3, 1990. http://www.theses.fr/1990TOU31542.

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ANDRE, BOUTHORS BLANDINE. "Evaluation diagnostique et pronostique des malformations uro-nephrologiques de decouverte antenatale." Lille 2, 1994. http://www.theses.fr/1994LIL2M316.

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BOISSINOT, FLORENCE. "Depistage echographique des uropathies malformatives : correlations ante et postnatales : a propos de 57 observations." Nantes, 1990. http://www.theses.fr/1990NANT068M.

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Bouttens-Marchand, Sylvie. "Analyse retrospective de 150 observations d'uropathies malformatives diagnostiquees entre 1981 et 1987 : apport du diagnostic antenatal par echographie." Amiens, 1988. http://www.theses.fr/1988AMIEM108.

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