scholarly journals Early Diagnosing of Urinary Tract Anomalies

2021 ◽  
Keyword(s):  
Urinary Tract ◽  
Urinary Tract Anomalies

UP-1.070: The Laparoscopic Approach in Patients with Upper Urinary Tract Anomalies

Urology ◽  
2009 ◽  
Vol 74 (4) ◽  
pp. S192
Author(s):  
J. Luptak ◽  
M. Vrany ◽  
B. Elias ◽  
J. Svihra ◽  
J. Kliment
Keyword(s):  
Urinary Tract ◽  
Laparoscopic Approach ◽  
Upper Urinary Tract ◽  
Urinary Tract Anomalies

scholarly journals Urinary tract anomalies in children with hypospadias

2010 ◽  
Vol 26 (12) ◽  
pp. 1237-1238 ◽  
Author(s):  
Tamara Faundez ◽  
Vincent Chariatte ◽  
Francois Cachat
Keyword(s):  
Urinary Tract ◽  
Urinary Tract Anomalies

scholarly journals Applicability of Magnetic Resonance Imaging in the Assessment of Fetal Urinary Tract Malformations

2019 ◽  
Vol 70 (1) ◽  
pp. 83-95 ◽  
Author(s):  
Tatiana Mendonça Fazecas ◽  
Edward Araujo Júnior ◽  
Heron Werner ◽  
Pedro Daltro ◽  
Alberto Borges Peixoto ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Urinary Tract ◽  
Magnetic Resonance ◽  
Three Dimensional ◽  
Surface Coil ◽  
Resonance Imaging ◽  
Magnetic Resonance Imaging Mri ◽  
Urinary Tract Malformations ◽  
Weighted Sequences ◽  
Urinary Tract Anomalies

Objective To assess the applicability of magnetic resonance imaging (MRI) to complement ultrasound in the diagnosis of fetal urinary tract anomalies. Methods This was a retrospective cohort study that included 41 women between 19 weeks and 37 weeks and 6 days of gestation carrying fetuses with malformations of the urinary tract which were initially diagnosed by ultrasound and then referred for MRI. In all cases, the diagnosis was confirmed after birth either through imaging or autopsy. A surface coil was positioned over the abdomen and T2-weighted sequences were obtained in the axial, coronal, and sagittal planes; T1 in at least one plane; and three-dimensional (3-D) TRUFI in fetuses with dilatation of the urinary tract. Results Mean gestational age at the time of MRI examination was 28.21 weeks. The rapid T2 sequences allowed all the anomalies of the fetal urinary tract to be assessed, whereas 3-D TRUFI sequencing proved very useful in evaluating anomalies involving dilatation of the urinary tract. The signs of pulmonary hypoplasia characterized by hypointense signal in the T2-weighted sequences were identified in 13 of the 41 fetuses. Conclusion MRI confirmed and added information to the ultrasound regarding fetal urinary tract anomalies, as well as information related to the other associated malformations, their progress in the prenatal period, and possible postnatal prognosis.

scholarly journals Antenatal Screening AndSonological Detection of Urinary Tract Anomalies.

2017 ◽  
Vol 16 (01) ◽  
pp. 09-15
Author(s):  
Mahale AjitR ◽  
Mahale Nina ◽  
Fernandes Merwyn ◽  
Ullal Sonali
Keyword(s):  
Urinary Tract ◽  
Antenatal Screening ◽  
Urinary Tract Anomalies

scholarly journals The Role of MRI in Evaluation of Fetal Urinary Tract Anomalies with Normal and Abnormal Volume Amniotic Fluid

2017 ◽  
Vol 4 (5) ◽  
Author(s):  
Dewi Asih Wirasasmita ◽  
Yarmaniani Miliati Muchtar ◽  
Gatot Abdurrazak ◽  
Sadina Pramukti Besar
Keyword(s):  
Urinary Tract ◽  
Amniotic Fluid ◽  
Abnormal Volume ◽  
Urinary Tract Anomalies

scholarly journals A Prolapsed Cecoureterocele in an Adult Treated Conservatively: Highly Rare, but Existent

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Löcherbach Florian ◽  
Preusser Stefan ◽  
Meier Mark
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Urinary Tract ◽  
Surgical Therapy ◽  
Surgical Procedure ◽  
Unusual Case ◽  
Ectopic Ureterocele ◽  
History Of ◽  
Urinary Tract Anomalies

Ectopic ureteroceles are one of the most common human urinary tract anomalies. They tend to be recognized and treated in early childhood, especially when they have prolapsed. In most cases surgical therapy is inevitable. In this case report, however, we present the unusual case of a 26-year-old woman suffering from a prolapsed cecoureterocele without any known history of an ectopic ureterocele so far. She was successfully treated without the need for a surgical procedure.

Urinary Tract Anomalies in Neonates With Spontaneous Pneumothorax and/or Pneumomediastinum

PEDIATRICS ◽  
1977 ◽  
Vol 59 (6) ◽  
pp. 1048-1049
Author(s):  
Bassam N. Bashour ◽  
J. Williamson Balfe
Keyword(s):  
Urinary Tract ◽  
Congenital Anomalies ◽  
Spontaneous Pneumothorax ◽  
Clinical Population ◽  
Live Births ◽  
Apparent Association ◽  
Urinary Tract Anomalies

Spontaneous pneumothorax is reportedly occurring in 0.05% to 1% of all live births.1,2 Pediatricians have long been aware of the apparent association between spontaneous pneumothorax, with or without pneumomediastinum, and congenital anomalies of the urinary tract. However, reports of the incidence of this relationship have been inconclusive, based on small numbers of infants.3-5 We therefore sought to determine this incidence in a large clinical population. METHODS We reviewed the records of all 6,236 infants admitted to the neonatology unit during 1961-1967 and selected all cases of spontaneous pneumothorax or pneumomediastinum or both (lung rupture) and of congenital urinary tract anomalies.

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