Obstructing Non-Refluxing Megaureter Secondary to Ectopic Ureter: a Rare Case Report
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Ended Megaureter in a 23-Year-Old Woman Causing Chronic Pain
341 Central European Journal of Urology CASE REPORT URINARY TRACT INFECTIONS The remnant of a congenital, blind- ended megaureter in a 23-year-old woman causing chronic pain and urinary infections Tomislav Pejcic1, Biljana Markovic2, Zoran Dzamic1, Milan Radovanovic1, Jovan Hadzi-Djokic3 1Clinical Center of Serbia, Urological Clinic, Belgrade, Serbia 2Clinical Center of Serbia, Institute of Radiology, Belgrade, Serbia 3Serbian Academy of Sciences and Arts, Belgrade, Serbia Article history Multicystic dysplastic kidney (MCDK) is a congenital anomaly as the result of abnormal interaction be- Received: March 31, 2103 tween the ureteric bud and metanephric mesenchyme. Unilateral MCDK can be associated with other Accepted: May 19, 2013 anomalies of the genitourinary tract. Relatively rare associated anomaly is the presence of ipsilateral Correspondence refluxing blind megaureter. Tomislav Pejcic The patient reported herein is a 23–years–old woman with involuted MCDK and ipsilateral blind mega- 129/9, Bulevar Zorana ureter causing chronic urinary infection and chronic abdominal pain. Preoperative and intraoperative Djindjica 11070 Belgrade, Serbia examination failed to detect the communication between megaureter and the urinary bladder. phone: +38 111 212 1616 [email protected] Key Words: multicystic dysplastic kidney ‹› refluxing blind megaureter INTRODUCTION CASE REPORT Multicystic dysplastic kidney (MCDK) is a congeni- A 23–year–old woman from a small village was sent tal anomaly that is the result of abnormal interac- to the urologist from the gynecologist, due to solitary tion between the ureteric bud and metanephric right kidney, cystic mass on the left side of the uri- mesenchyme, early ureteral obstruction, or ureteral nary bladder and the presence of chronic pain and atresia. -
Acute Onset Flank Pain-Suspicion of Stone Disease (Urolithiasis)
Date of origin: 1995 Last review date: 2015 American College of Radiology ® ACR Appropriateness Criteria Clinical Condition: Acute Onset Flank Pain—Suspicion of Stone Disease (Urolithiasis) Variant 1: Suspicion of stone disease. Radiologic Procedure Rating Comments RRL* CT abdomen and pelvis without IV 8 Reduced-dose techniques are preferred. contrast ☢☢☢ This procedure is indicated if CT without contrast does not explain pain or reveals CT abdomen and pelvis without and with 6 an abnormality that should be further IV contrast ☢☢☢☢ assessed with contrast (eg, stone versus phleboliths). US color Doppler kidneys and bladder 6 O retroperitoneal Radiography intravenous urography 4 ☢☢☢ MRI abdomen and pelvis without IV 4 MR urography. O contrast MRI abdomen and pelvis without and with 4 MR urography. O IV contrast This procedure can be performed with US X-ray abdomen and pelvis (KUB) 3 as an alternative to NCCT. ☢☢ CT abdomen and pelvis with IV contrast 2 ☢☢☢ *Relative Rating Scale: 1,2,3 Usually not appropriate; 4,5,6 May be appropriate; 7,8,9 Usually appropriate Radiation Level Variant 2: Recurrent symptoms of stone disease. Radiologic Procedure Rating Comments RRL* CT abdomen and pelvis without IV 7 Reduced-dose techniques are preferred. contrast ☢☢☢ This procedure is indicated in an emergent setting for acute management to evaluate for hydronephrosis. For planning and US color Doppler kidneys and bladder 7 intervention, US is generally not adequate O retroperitoneal and CT is complementary as CT more accurately characterizes stone size and location. This procedure is indicated if CT without contrast does not explain pain or reveals CT abdomen and pelvis without and with 6 an abnormality that should be further IV contrast ☢☢☢☢ assessed with contrast (eg, stone versus phleboliths). -
Effectiveness of Ureteric Reimplantation on Non-Refluxing Obstructive
EFFECTIVENESS OF URETERIC REIMPLANTATION ON NON-REFLUXING OBSTRUCTIVE CONGENITAL MEGAURETER SHAFIQUR RAHMAN1, MOHAMMAD ABDUL AZIZ1, MM HASAN1, NURUN NAHAR HAPPY2, TASNEEM MAHJABEEN3 1Department of Urology, BIRDEM General Hospital, Dhaka, 2Department of Plastic Surgery and 100 Bed Burn Unit, DMC & H, Dhaka, 3Department of Dermatology, BIRDEM General Hospital, Dhaka Abstract: Background: One in ten thousand children born with megaureter. A significant portion of this groups are of obstructed variety and the rest are refluxing ureter. It can cause obstructions and back pressure renal damage. Early diagnosis and treatment can stop deterioration of renal function and prevent complications like renal failure. Definitive treatment is uretero-neocystostomy with or without tailoring the ureter. Objective: Objective of this study was to observe the effectiveness of ureteric reimplantation on non-refluxing obstructive congenital megaureter. To achieve this objective we had observed serum creatinine level pre and postoperatively and assessed structural changes in kidney by ultrasonogram, IVU, MCU and RGP pre and postoperatively. We also observed the split renal function and split GFR of the affected kidney both pre and post operatively. Methods: This was a cross-sectional observational study. This study comprise of 35 cases of congenital non-refluxing obstructed megaureter, who were admitted in BIRDEM General Hospital and multiple other hospitals in Dhaka city from July 2013 to December 2014. Diagnosis was made by intravenous urography (IVU) reveling a dilated lower third or entire ureter with narrow tapering lower end. Obstruction was also confirmed by diuretic Tc99m DTPA scan. A voiding cystourethrogram was obtained to exclude VUR. Those with poor renal function were evaluated by ultrasonography, DTPA scan and retrograde ureteropyelography. -
URINARY TRACT INFECTION (UTI) ALGORITHM- UTI Testing
CLINICAL PATHWAY URINARY TRACT INFECTION (UTI) ALGORITHM- UTI Testing Suspicion of UTI Intended for: • Patients with presumed UTI • Greater than 60days of age Age Age NOT intended for: Age 60days- >36months or • Known urologic anomalies <60days • 36months Toilet Trained Chronic/complex conditions (ie. spinabifida, self cath, hardware, etc.) • Recent urinary tract instrumentation Clean Catch UA placement Cath UA • Critical Illness Refer to CCG Consider • Immunocompromised Fever? NO “Fever, infant (less Alternative Dx than 28days or 28- 90days)” Index of UA Result? Neg Low Consider Suspicion* Alternative Dx Yes Pos/Equiv High *Index of Suspicion • Febrile Culture Culture • Dysuria • Frequency • Flank Pain • Hx of UTI History of No Gender? Male Circumcised? YES UTI? Male Female Risk Factors Yes NO Female Risk Factors • Temp ≥ 39°C • Age <12mo • Fever ≥2 days • Temp ≥ 39°C • No source of • ≥ 3 Risk Fever ≥ 2 days infection • No source of ≥ 3 Risk • Non-black Factors? <1yr? No infection Factors? Race • White Race Yes Yes No Yes No Cath UA Consider Cath Cath UA + Cath UA Consider Cath + Culture Cath UA based on Culture + Culture based on ! + Culture clinical clinical Bag Specimen presentation presentation NOT Preferred Neg Neg (consider with labial adhesions, or failed catheterizations) Consider Consider NEVER send culture Alternative Dx Alternative Dx Imaging Recommendations for patients >2months after 1st Febrile UTI No imaging required o Prompt response to therapy (afebrile in 72 hrs) o Reliable outpatient follow up o Normal voiding pattern -
Impact of Urolithiasis and Hydronephrosis on Acute Kidney Injury in Patients with Urinary Tract Infection
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.13.200337; this version posted July 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Impact of urolithiasis and hydronephrosis on acute kidney injury in patients with urinary tract infection Short title: Impact of urolithiasis and hydronephrosis on AKI in UTI Chih-Yen Hsiao1,2, Tsung-Hsien Chen1, Yi-Chien Lee3,4, Ming-Cheng Wang5,* 1Division of Nephrology, Department of Internal Medicine, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi, Taiwan 2Department of Hospital and Health Care Administration, Chia Nan University of Pharmacy and Science, Tainan, Taiwan 3Department of Internal Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei, Taiwan 4School of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei, Taiwan 5Division of Nephrology, Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan *[email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.07.13.200337; this version posted July 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Abstract Background: Urolithiasis is a common cause of urinary tract obstruction and urinary tract infection (UTI). This study aimed to identify whether urolithiasis with or without hydronephrosis has an impact on acute kidney injury (AKI) in patients with UTI. -
Obstructive Nephropathy Saulo Klahr
REVIEW ARTICLE Obstructive Nephropathy Saulo Klahr Abstract ages. The incidence of hydronephrosis reported by Bell (1) in a series of32,360 autopsies was 3.8% (3.9% in males, 3.6% in Obstructive nephropathy is a relatively commonentity females). The incidence of clinical manifestations of obstruc- that is treatable and often reversible. It occurs at all ages tive uropathy prior to death was not reported, and it is likely from infancy to elderly subjects. Obstructive uropathy is that hydronephrosis was an incidental finding in many of these classified according to the degree, duration and site of the patients. The incidence of hydronephrosis at autopsy is some- obstruction. It is the result of functional or anatomic le- what lower in children than in adults, being 2%in one series of sions located in the urinary tract. The causes of obstructive 16, 100 autopsies (2). Over 80% of children with hydronephro- uropathy are many. Obstruction of the urinary tract may sis at autopsy were less than 1 year old, with the balance of decrease renal blood flow and the glomerular filtration rate. childhood cases being distributed uniformly through the child- Several abnormalities in tubular function mayoccur in hood years. About 166 patients per 100,000 population had a obstructive nephropathy. These include decreased reab- presumptive diagnosis of obstructive uropathy on admission sorption of solutes and water, inability to concentrate the to hospitals in the United States in 1985 (3). Amongmale pa- urine and impaired excretion of hydrogen and potassium. tients with kidney and urologic disorders, obstructive uropa- Renal interstitial fibrosis is a commonfinding in patients thy ranked fourth at discharge (242 patients/100,000 dis- with long-term obstructive uropathy. -
Evolving Concepts in Human Renal Dysplasia
DISEASE OF THE MONTH J Am Soc Nephrol 15: 998–1007, 2004 EBERHARD RITZ, FEATURE EDITOR Evolving Concepts in Human Renal Dysplasia ADRIAN S. WOOLF, KAREN L. PRICE, PETER J. SCAMBLER, and PAUL J.D. WINYARD Nephro-Urology and Molecular Medicine Units, Institute of Child Health, University College London, London, United Kingdom Abstract. Human renal dysplasia is a collection of disorders in correlating with perturbed cell turnover and maturation. Mu- which kidneys begin to form but then fail to differentiate into tations of nephrogenesis genes have been defined in multiorgan normal nephrons and collecting ducts. Dysplasia is the princi- dysmorphic disorders in which renal dysplasia can feature, pal cause of childhood end-stage renal failure. Two main including Fraser, renal cysts and diabetes, and Kallmann syn- theories have been considered in its pathogenesis: A primary dromes. Here, it is possible to begin to understand the normal failure of ureteric bud activity and a disruption produced by nephrogenic function of the wild-type proteins and understand fetal urinary flow impairment. Recent studies have docu- how mutations might cause aberrant organogenesis. mented deregulation of gene expression in human dysplasia, Congenital anomalies of the kidney and urinary tract and the main renal pathology is renal dysplasia (RD). In her (CAKUT) account for one third of all anomalies detected by landmark book Normal and Abnormal Development of the routine fetal ultrasonography (1). A recent UK audit of child- Kidney published in 1972 (7), Edith Potter emphasized that one hood end-stage renal failure reported that CAKUT was the must understand normal development to generate realistic hy- cause in ~40% of 882 individuals (2). -
Primary Obstructive Megaureter in a Child: a Case Report and Review of Literature
Case Report Annals of Pediatric Research Published: 10 May, 2019 Primary Obstructive Megaureter in a Child: A Case Report and Review of Literature Volkan Sarper Erikci* and Tunahan Altundag Department of Pediatric Surgery, Tepecik Training Hospital, Turkey Abstract Ureterovesical Junction Obstruction (UVJO) is a rare but important cause of hydroureteronephrosis in childhood. A 2-years-old boy suffered from giant hydroureteronephrosis originating from idiopathic ureterovesical junction obstruction. He was treated with excision of narrow ureteric segment with tapering ureteroplasty and a ureteral reimplantation was performed. This case is presented and discussed with reference to etiology of this rather rare anomaly. Keywords: Hydroureteronephrosis; Ureterovesical junction obstruction; Children Introduction Congenital Ureterovesical Junction Obstruction (UVJO) may be observed during fetal age or any stage at the time of childhood. It is aimed in this report to present a male child with obstructive megaureter due to congenital UVJO. He was surgically treated with excision of narrowed distal ureter in addition to tapering ureteroplasty with ureteroneocystostomy. The topic is discussed with special reference to the etiology of this rather rare entity under the light of relevant literature. Case Presentation A 27-months-old boy was admitted to our department with an antenatal history of right Hydroureteronephrosis (HUN). Laboratory tests were otherwise normal except signs of Urinary OPEN ACCESS Tract Infection (UTI) including leucocyturia. -
The Presentation and Management of Neonatal Obstructive Uropathies J
Postgrad Med J: first published as 10.1136/pgmj.48.562.486 on 1 August 1972. Downloaded from Postgraduate Medical Journal (August 1972) 48, 486 -492. The presentation and management of neonatal obstructive uropathies J. H. JOHNSTON F.R.C.S. Alder Hey Children's Hospital, Liverpool Presentation urinary, alimentary and genital tracts share a The existence of a congenital urinary obstruction common evacuatory channel is similarly frequently may be suggested when routine examination of the associated with upper urinary tract lesions. newborn infant reveals such signs as enlargement of one or both kidneys, distension of the bladder or (3) Anomalies of the female genital tract slow, dribbling micturition. The paediatrician should Congenital absence of the vagina is associated also be alerted to the possibility of obstructive uro- with urinary tract anomalies in some 500 of cases pathy when there are present non-urological con- (Bryan, Nigro & Counsellor, 1949). A similar high genital anomalies which often secondarily involve incidence occurs with such conditions as duplication the urinary tract or which are known commonly to ofthe vagina and uterus but these may not be obvious co-exist with congenital urinary tract lesions. clinically in the young child. Secondary involvement, with obstruction, of the urinary tract occurs with space-occupying masses in Deficient abdominal mucsculature (4) by copyright. the pelvis such as hydrometrocolpos or a large intra- Urinary tract anomalies of various degrees of pelvic component of a sacrococcygeal teratoma. are The pelvic tumour, by displacing the bladder, leads severity always present. to chronic urinary retention and upper tract dilata- Cardiac anomalies tion. -
Irish Rare Kidney Disease Network (IRKDN)
Irish Rare kidney Disease Network (IRKDN) Others Cork University Mater, Waterford University Dr Liam Plant Hospital Galway Dr Abernathy University Hospital Renal imaging Dr M Morrin Prof Griffin Temple St and Crumlin Beaumont Hospital CHILDRENS Hospital Tallaght St Vincents Dr Atiff Awann Rare Kidney Disease Clinic Hospital University Hospital Prof Peter Conlon Dr Lavin Prof Dr Holian Little Renal pathology Lab Limerick University Dr Dorman and Hospital Dr Doyle Dr Casserly Patient Renal Council Genetics St James Laboratory Hospital RCSI Dr Griffin Prof Cavaller MISION Provision of care to patients with Rare Kidney Disease based on best available medical evidence through collaboration within Ireland and Europe Making available clinical trials for rare kidney disease to Irish patients where available Collaboration with other centres in Europe treating rare kidney disease Education of Irish nephrologists on rare Kidney Disease. Ensuring a seamless transition of children from children’s hospital with rare kidney disease to adult centres with sharing of knowledge of rare paediatric kidney disease with adult centres The provision of precise molecular diagnosis of patients with rare kidney disease The provision of therapeutic plan based on understanding of molecular diagnosis where available Development of rare disease specific registries within national renal It platform ( Emed) Structure Beaumont Hospital will act as National rare Kidney Disease Coordinating centre working in conjunction with a network of Renal unit across the country -
Supermicar Data Entry Instructions, 2007 363 Pp. Pdf Icon[PDF
SUPERMICAR TABLE OF CONTENTS Chapter I - Introduction to SuperMICAR ........................................... 1 A. History and Background .............................................. 1 Chapter II – The Death Certificate ..................................................... 3 Exercise 1 – Reading Death Certificate ........................... 7 Chapter III Basic Data Entry Instructions ....................................... 12 A. Creating a SuperMICAR File ....................................... 14 B. Entering and Saving Certificate Data........................... 18 C. Adding Certificates using SuperMICAR....................... 19 1. Opening a file........................................................ 19 2. Certificate.............................................................. 19 3. Sex........................................................................ 20 4. Date of Death........................................................ 20 5. Age: Number of Units ........................................... 20 6. Age: Unit............................................................... 20 7. Part I, Cause of Death .......................................... 21 8. Duration ................................................................ 22 9. Part II, Cause of Death ......................................... 22 10. Was Autopsy Performed....................................... 23 11. Were Autopsy Findings Available ......................... 23 12. Tobacco................................................................ 24 13. Pregnancy............................................................ -
Acute Necrotizing Ureteritis with Obstructive Uropathy Following Instillation of Silver Nitrate in Chyluria: a Case Report
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector C.M. Su, Y.C. Lee, W.J. Wu, et al ACUTE NECROTIZING URETERITIS WITH OBSTRUCTIVE UROPATHY FOLLOWING INSTILLATION OF SILVER NITRATE IN CHYLURIA: A CASE REPORT Chin-Ming Su, Yung-Chin Lee, Wen-Jen Wu, Hung-Lung Ke, Yii-Her Chou, and Chun-Hsiung Huang Department of Urology, Kaohsiung Medical University, Kaohsiung, Taiwan. Chyluria occurs as a result of communication between the lymphatics and the renal pelvis. It is believed that instillation of silver nitrate into the renal pelvis is a safe, minimally invasive and effective treatment for chyluria. We report an unusual complication of acute necrotizing ureteritis following instillation of silver nitrate in a case of chyluria. It resolved completely with non-surgical intervention. The diagnosis and management of chyluria is discussed, with a brief review of the literature. Key Words: chyluria, silver nitrate instillation, necrotizing ureteritis (Kaohsiung J Med Sci 2004;20:512–5) Chyluria occurs as a result of communication between the radiation, or parasite infection were known. The patient lymphatics and the renal pelvis. Its etiology may be classi- underwent cystoscopic examination following a fatty fied as parasitic or non-parasitic. Although the disease is meal. A milky efflux was observed from the right ureteral not life-threatening, it may cause hypoproteinemia, weight orifice. Retrograde pyelography was normal, with no loss, and immunologic disorders due to severe proteinuria pyelolymphatic backflow (Figure 1). Under the diagnosis of [1]. The treatment of chyluria includes limitation of diet to chyluria, 10 mL of 1% silver nitrate was instilled through a mid-chain triglycerides, instillation of silver nitrate, and ureteric catheter.