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Books on the topic 'Hydronephrosis'

To see the other types of publications on this topic, follow the link: Hydronephrosis.

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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1

García, Barbara Marie. The ultrasonographic differentiation of obstructive vs. nonobstructive hydronephrosis in children: A multivariate scoring system. [New Haven, Conn: s.n.], 1995.

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2

C, Anderson James. Hydronephrosis. Elsevier Science & Technology Books, 2017.

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3

Gosling, J. A., P. H. O'Reilly, and E. C. Edwards. Idiopathic Hydronephrosis. Springer, 2011.

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4

Gosling, J. A., P. H. O'Reilly, and E. C. Edwards. Idiopathic Hydronephrosis. Springer London, Limited, 2012.

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5

Karanfilovski, Vlatko. Renal Lymphangiectasia: An Unusual Mimicker of Hydronephrosis. BAYSHOP (Generis Publishing), 2022.

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6

Cure Hydronephrosis: The Complete Guide On Everything You Need To Know About Hydronephrosis Cure, Treatment, Prevention And Diet. Independently published, 2021.

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7

Onen, Abdurrahman, Ali Avanoglu, Luis Henrique Braga, and Venkata R. Jayanthi, eds. Hydronephrosis Associated with Ureteropelvic Junction Anomalies: An Ongoing Challenge. Frontiers Media SA, 2022. http://dx.doi.org/10.3389/978-2-88976-184-5.

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8

Publications, ICON Health. Hydronephrosis - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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9

Wahlin, Nils. Hydronephrosis in Childhood: An Experimental and Clinical Study (Comprehensive Summaries of Uppsala Dissertations, 934). Uppsala Universitet, 2000.

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10

Fox, Grenville, Nicholas Hoque, and Timothy Watts. Endocrinology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198703952.003.0016.

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This chapter provides background information on fetal and neonatal renal development, physiology, and function. Detailed information is given on management of common, antenatally diagnosed, renal anomalies (renal pelvis dilatation/hydronephrosis); post-natal diagnoses (hypospadius, hydrocele); posterior urethral valves; polycystic kidney disease; and rarer diagnoses. There is a guideline on the management of acute renal failure in the newborn, and information on dialysis.

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11

Yaqoob, Muhammad M., Katherine Bennett-Richards, and Islam Junaid. The patient with urinary tract obstruction. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0356.

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Several terms usually describe obstruction of the urinary tract and its consequences such as hydronephrosis, obstructive uropathy, and obstructive nephropathy. Obstruction can be due to anatomical or functional abnormalities of the urethra, bladder, ureter, or renal pelvis. These abnormalities can be congenital or acquired. Obstructive uropathy also can occur during the course of diseases extrinsic to the urinary tract. This is a reversible cause of renal impairment and calls for urgent diagnosis and treatment to prevent chronic irreversible renal scarring and consequent progressive chronic renal disease.

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12

Schreuder, Michiel F. Anatomical types of congenital anomalies. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0345.

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Antenatal hydronephrosis is the most common abnormality detected during antenatal ultrasound screening (1 in 100–500 pregnancies). Depending on the degree of dilatation, postnatal evaluation with ultrasound and/or renography is indicated to detect urinary tract obstruction. Obstruction can be found at various levels of the urinary tract such as the pyeloureteric junction, vesicoureteric junction (resulting in a megaureter), and lower urinary tract (most commonly posterior urethral valves). The decision to surgically correct obstruction can be challenging to make, and additional markers (both radiological as urinary) are needed but are not yet available in daily practice.

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13

Narsinh, Kazim, and Thomas Kinney. The Air Technique to Determine Appropriate Posterior Calyx for Puncture. Edited by S. Lowell Kahn, Bulent Arslan, and Abdulrahman Masrani. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199986071.003.0089.

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A posterior calyx is the preferred point of entry into the urinary collecting system during percutaneous nephrostomy procedures. Although ultrasonographic guidance is the preferred modality to gain this initial access, confident identification of a posterior calyx can be challenging using sonography alone, particularly in obese patients without hydronephrosis. In this setting, air or carbon dioxide can be introduced into the prone patient’s collecting system in order to fluoroscopically guide a confident puncture of the posterior calyx of the renal collecting system. This chapter presents a technique employing the introduction of air into the urinary collecting system to permit facile identification of a posterior calyx using fluoroscopic guidance during percutaneous nephrostomy procedures.

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14

Schreuder, Michiel F. Pelviureteric junction obstruction and megaureter in children. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0353.

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Two main sites of urine flow obstruction in the upper urinary tract are located at the pelviureteric and vesicoureteric junctions, both of which result in urinary tract dilatation. With current antenatal ultrasound screening, most patients are identified before birth, and 10–30% of infants with antenatal hydronephrosis are found to have pelviureteric junction obstruction, and 5–10% vesicoureteric junction obstruction/megaureter. In addition, a megaureter can also be based on urine reflux, even in combination with obstruction, or be a non-refluxing non-obstructed megaureter. In case of obstruction, surgery may be indicated, but identifying cases that need to be operated on is challenging and no good marker to assist in this differentiation is available yet.

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15

Schreuder, Michiel F. Duplex, ectopic, and horseshoe kidneys. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0352.

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A duplex urinary tract, irrespective of the degree of duplication, is present in 0.8% at autopsy, of which about 20–35% is bilateral. The majority of duplex systems are incomplete, indicating that the ipsilateral ureters fuse before entering the bladder. A complete duplex system shows anomalies of the upper moiety, with associated ureterocele or ectopic ureter, and of the lower moiety, frequently associated with vesicoureteral reflux. Renal ectopia is a rare (1/1000) congenital defect where the kidney is not located in the renal fossa, and is associated with a high rate of hydronephrosis, vesicoureteral reflux, and abnormal contralateral kidney. In a horseshoe kidney (present in 1/400 to 1/1800), fusion of the two kidneys takes place, but the two renal moieties are still located on both sides of the midline. As the lower poles are fused in the midline, a horseshoe kidney is usually located lower than normal and orientation of the renal axis is shifted, which may guide diagnosis during abdominal ultrasound.

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16

Raphaelson, Lilli. Zur Frage der Hydronephrose Bei Infantiler Phimose. Springer London, Limited, 2013.

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17

Lichtenberg, A. v. Handbuch der Urologie : Band 4 : Spezielle Urologie II: Tuberkulose. Aktinomykose. Syphilis. Steinkrankheiten. Hydronephrose. Wanderniere. Nierengeschwülste. Stoffwechselstörungen. Tropenkrankheiten. Springer London, Limited, 2013.

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