RENAL SCINTIGRAPHY in the 21St CENTURY

Total Page:16

File Type:pdf, Size:1020Kb

RENAL SCINTIGRAPHY in the 21St CENTURY RENAL SCINTIGRAPHY IN THE 21st CENTURY 99m Tc- MAG3 with zero time injection of Furosemide (MAG3-F0) : A Fast and Easy Protocol, One for All Indications Clinical Experience Congenital Disorders PROTOCOL FOR MAG3 - F0 PATIENT PREPARATION Easy (only restriction, oral hydration, no bladder cath.) DYNAMIC STUDY (iv 1-10 mCi MAG3 + 40-80 mg LASIX) Simultaneous injection of Furosemide: MAG3-F0 Duration of the study 25 min TOMOGRAPHY-SPECT (20 mCi MAG3) No diuretic needed Duration of the study 4 min RENAL SCINTIGRAPHY AT UM/JMMC: (MAG3-F0) Method applied the last 18 years: FOR NATIVE KIDNEY STUDIES FOR RENAL TRANSPLANT STUDIES RENAL SCINTIGRAPHY AT UM/JMMC: (MAG3-F0) Method applied the last 18 years: A. DYNAMIC STUDY Injection iv 1-10 mCi MAG3 + 40-80 mg LASIX (Furosemide) Simultaneous Injection of MAG3 and Lasix = F0 ACQUISITION: FLOW: 1 min ( 1 frame per 1 sec) FUNCTION: 22 min ( 1 frame per 30 sec) POST VOID 2 min static image (at 25-30 min) DELAYED 2 min static images (at 1 hr) GROUPING IMAGES : -FLOW: in 3 sec images -FUNCTION: in 2 min images GRAPH GENERATION: -FLOW/FUNCTION, KIDNEY/CORTEX RENAL SCINTIGRAPHY AT UM/JMMC: (MAG3-F0) Method applied the last 18 years: This protocol was originally applied in the evaluation of drainage Soon it was realized that it allowed the evaluation of the parenchyma Then it was applied in all parenchymal indications (including APN) It was also utilized for the study of Renovascular Hypertension In children allowed the study of HIV and other Nephropathies In patients with renal colic unraveled the Stunned (decompressed) kidney It was finally successful in the study of complications of renal transplants MAG3-F0 PROTOCOL Misconception • You cannot image the kidneys of a newborn • You need to catheterize the urinary bladder to exclude obstruction Facts • MAG3 -F0 works in the Newborn Infant • You do not need to catheterize the urinary bladder Typical NORMAL MAG3-F0 in a NEWBORN Indication: Evaluate Pelviectasis found by Ultrasound Normal study; Slight Immaturity, Bladder empties Typical NORMAL MAG3-F0 in a NEWBORN Indication: Evaluate Pelviectasis found by Ultrasound Normal study; Slight Immaturity, Bladder does not empty MAG3-F0 in a 10 yo CHILD; Mature Normal Kidneys Indication: Evaluate effects of urinary infection Slight discrepancy in size and function (effect of infection on the right kidney) Normal MAG3 -F0 in an ADULT Indication: Renal Colic INDICATIONS FOR MAG3-F0 STUDIES: DIAGNOSIS - PROGNOSIS - FOLLOW UP • PARENCHYMAL OR DRAINAGE DISORDERS • IN CONGENITAL OR ACQUIRED DISEASES • FOR NATIVE OR TRANSPLANTED KIDNEYS • AT ALL AGES AND FUNCTIONAL STATES CONGENITAL URINARY TRACT ANOMALIES MAG3-F0 Dynamic Studies Diagnosis-Prognosis-Follow up MOST COMMON INDICATIONS FOR RENAL SCINTIGRAPHY NEONATE • CONGENITAL RENAL INSUFFICIENCY/FAILURE PERINATAL COMPLICATIONS WORK UP OF SONOGRAPHIC FINDINGS MASSES IN THE ABDOMEN SEARCH FOR AND EVALUATION OF CONGENITAL UT ANOMALIES Diagnosis-Prognosis-Follow up MAG3 -F0 in Congenital Renal Insufficiency or Failure Posterior Urethral Valves Bilateral Agenesis Bilateral Dysplasia CONGENITAL RENAL INSUFFICIENCY/FAILURE Bilateral Obstruction Early Correction of UPJO (the first week of life) may Prevent Loss of Function and may Promote Recovery of Function Congenital renal insufficiency/failure Posterior Urethral Valves in the Newborn Bilateral Obstruction Congenital renal insufficiency/failure Bilateral Agenesis 2 min 20 min Congenital renal insufficiency/failure Bilateral Dysplasia in the newborn 2 min 4 10 12 CONGENITAL RENAL INSUFFICIENCY/FAILURE Bilateral Dysplasias • Bilateral Dysplasias or Agenesis • No functioning renal parenchyma • No Intervention indicated, no recovery expected MOST COMMON INDICATIONS FOR RENAL SCINTIGRAPHY NEONATE CONGENITAL RENAL INSUFFICIENCY/FAILURE • PERINATAL COMPLICATIONS WORK UP OF SONOGRAPHIC FINDINGS MASSES IN THE ABDOMEN SEARCH FOR AND EVALUATION OF CONGENITAL UT ANOMALIES Diagnosis-Prognosis-Follow up MAG3 -F0 in Perinatal Renal Disorders Acute Tubular Necrosis Renovascular Hypertension Adrenal Hemorrhage Normal size Solid kidneys, Preservation of Flow and Cortical Uptake; Delayed Drainage; High Residual Cortical Activity: Acute Tubular Necrosis: No intervention; Full Recovery Perinatal Renal Insufficiency/Failure: Newborn with Severe Oliguria Diabetic Mother and Difficult, Prolonged Delivery Neonates with hypertension from renal ischemia due to thrombus in the umbilical catheter should not be treated with ACE-Inhibitors Neonatal Hypertension from Aortic Thrombus Around Aortic Catheter Left Infarction Right Ischemia MAG3 -F0 in Neonatal Hypertension from renal ischemia due to thrombus around the umbilical catheter Baseline Renogram ACE Inhibition Renogram This infant should not be treated with ACE-Inhibitors Perinatal Adrenal Hemorrhage MOST COMMON INDICATIONS FOR RENAL SCINTIGRAPHY NEONATE INFANT OR OLDER CHILD CONGENITAL RENAL INSUFFICIENCY/FAILURE PERINATAL COMPLICATIONS • WORK UP OF SONOGRAPHIC FINDINGS • MASSES IN THE ABDOMEN • SEARCH FOR AND EVALUATION OF CONGENITAL UT ANOMALIES Diagnosis-Prognosis-Follow up MAG3 -F0 in Congenital Non-Obstructing Renal Diseases Unilateral Agenesis Hypoplasia Ectopia Horse-shoe kidney Multicystic Kidney Disease Polycystic Kidney Disease Megaureter Agenesis Hypoplasia with contralateral Compensatory Hypertrophy 2 min kc 20 min Ectopic normal kidney (pelvic) Ectopic esp. normal kidneys are missed about 50% by routine Ultrasonography but they can very easily be identified by MAG3 -F0, within 2 min after injection Horseshoe Kidney Non-obstructed Multicystic Dysplastic Kidney Multicystic Dysplastic Kidney Multicystic Dysplastic Kidney Polycystic Kidney Disease Autosomal Recessive 2 min 4 12 14 Mild infantile type 18 20 Polycystic Kidney Disease Children: Autosomal Recessive Other congenital diseases (Scan: Large kidneys with DPD) Adults: Autosomal Dominant (Scan: Large kidneys with evidence of multiple cysts) Polycystic Kidney Disease Autosomal Dominant (usually in adults) Cysts Normal drainage MEGAURETER without OBSTRUCTION Use of Bladder Catheterization FOLLOW UP Idiopathic NEWBORN Megaureter 2 min 2 min 20 min Delayed NEWBORN FOLLOW UP NEUROGENIC BLADDER MAG3 -F0 in Congenital Renal Obstruction Anatomic Uretero-Pelvic Junction Obstruction Uretero-Vesical Junction Obstruction Posterior Urethral Valves Functional Vesico-Ureteral Reflux OBSTRUCTION Can we prevent the loss? Neonate 5 year old Proximal Obstruction ( Uretero-Pelvic Junction ) 2min 4 10 12 25min 18 20 Distal Obstruction ( Uretero-Vesical Junction ) 2min 4 10 12 kc 18 20 25min Pelvic Ectopic Obstructed Kidney (UPJO) 2 min 4 min 6 min Contrast enhanced images Findings: Early Defect and Late Retention Left Upper Pole Defect Urinary Bladder Diagnosis: Duplication with Upper Moiety Obstruction, Ectopic Ureter, and Ureterocele Newborn with abnormal prenatal ultrasound Findings: Early Defect and Late Retention Left Upper Pole Defect Urinary Bladder Diagnosis: Duplication with Upper Moiety Obstruction, Ectopic Ureter, and Ureterocele One and ½ month old with abnormal ultrasound referred from outside for evaluation Duplication with Ectopic Ureter Ureterocele and Upper Moiety Obstruction THE VALUE OF MAG3 -F0 DIURETIC RENOGRAPHY IN PREDICTING THE NEED FOR SURGERY IN THE NEONATE WITH URETEROPELVIC JUNCTION OBSTRUCTION Sfakianakis G, Vensel E, Tapia M, Policaro F, Gosalbez R, Labbie A, Zilleruelo G, Abitbol C, Montane B, Strauss J Abstract: SNM 2000 Right Pelvic Retention but Normal Drainage of the Cortex and Downsloping Renogram Prognosis: High probability for Spontaneous Compensation; Surgery Not Needed SRF 45/55 L/R Follow up study shows Improvement of Drainage and Preservation of Renal Function SRF 50/50 L/R Newborn with pelviectasis evaluated for obstruction Newborn A down-sloping MAG3-F0 renography in the neonate predicts 6 mo old Spontaneous Compensation High Pelvic Retention; Abnormal Drainage of the Cortex and Upsloping Renogram: UPJO Prognosis: No probability for Spontaneous Compensation; Surgery is Needed The infant was not operated but was followed up with scintigraphy Follow up study shows Deterioration of Drainage and Loss of Renal Function Newborn with severe pelvicaliectasis evaluated for obstruction Newborn An Up-sloping MAG3-F0 renography in the neonate predicts 1 mo old The need of Surgical Correction A Horizontal Renogram requires follow up studies FOLLOW UP STUDIES Follow Up Studies Horse-shoe kidney non obstructed; newborn and 6 year old Follow Up Effect of Therapy Posterior Urethral Valves Newborn At birth Post Therapy S/P Therapy Posterior Urethral Valves Congenital renal insufficiency/failure Posterior Urethral Valves in the Newborn and F/U post therapy Recent Observations When the dilated collecting system keeps the activity but the CORTEX EMPTIES: there is no functional obstruction (reservoir effect) or there is no obstruction at all MAG3 -F0 in Renal Obstruction: New Findings Traditional concept: To make the Diagnosis of Obstruction you need to Study the Renogram and the Collecting System of the Kidney New Horizons: To make the Diagnosis of Obstruction you better study the behavior of the Renal Parenchyma: If the Parenchyma empties, there is no obstruction! (even when the drainage system is dilated and it does not empty appropriately) Clinical Experience on The Discrepancy between the Parenchyma (Empties appropriately) and the Drainage System (suggests Obstruction) • Different categories of patients with Congenital or Acquired disorders • Frequent finding in patients with chronic problems • Data were presented
Recommended publications
  • Renal Agenesis, Renal Tubular Dysgenesis, and Polycystic Renal Diseases
    Developmental & Structural Anomalies of the Genitourinary Tract DR. Alao MA Bowen University Teach Hosp Ogbomoso Picture test Introduction • Congenital Anomalies of the Kidney & Urinary Tract (CAKUT) Objectives • To review the embryogenesis of UGS and dysmorphogenesis of CAKUT • To describe the common CAKUT in children • To emphasize the role of imaging in the diagnosis of CAKUT Introduction •CAKUT refers to gross structural anomalies of the kidneys and or urinary tract present at birth. •Malformation of the renal parenchyma resulting in failure of normal nephron development as seen in renal dysplasia, renal agenesis, renal tubular dysgenesis, and polycystic renal diseases. Introduction •Abnormalities of embryonic migration of the kidneys as seen in renal ectopy (eg, pelvic kidney) and fusion anomalies, such as horseshoe kidney. •Abnormalities of the developing urinary collecting system as seen in duplicate collecting systems, posterior urethral valves, and ureteropelvic junction obstruction. Introduction •Prevalence is about 3-6 per 1000 births •CAKUT is one of the commonest anomalies found in human. •It constitute approximately 20 to 30 percent of all anomalies identified in the prenatal period •The presence of CAKUT in a child raises the chances of finding congenital anomalies of other organ-systems Why the interest in CAKUT? •Worldwide, CAKUT plays a causative role in 30 to 50 percent of cases of end-stage renal disease (ESRD), •The presence of CAKUT, especially ones affecting the bladder and lower tract adversely affects outcome of kidney graft after transplantation Why the interest in CAKUT? •They significantly predispose the children to UTI and urinary calculi •They may be the underlying basis for urinary incontinence Genes & Environment Interact to cause CAKUT? • Tens of different genes with role in nephrogenesis have been identified.
    [Show full text]
  • A Study of Congenital Renal Anomalies in Adult Cadavers
    Original Research Article DOI: 10.18231/2394-2126.2017.0045 A study of congenital renal anomalies in adult cadavers Pabbati Raji Reddy Associate Professor, RVM Institute of Medical Sciences & Research Center, Telangana Email: [email protected] Abstract Introduction: Congenital abnormalities of the kidneys and urinary tract play a major role in the morbidity and mortality. Many of these renal anomalies predispose to obstruction which lay lead to renal failure. We had in our study observed the different malformations in human kidneys among the adults human cadavers. Materials and Method: 50 cadavers who died of renal failure and were scheduled for post mortem were included in the study. The position of the suprarenal gland and the upper poles of the kidneys, the size, shape and the kidneys, the arrangement of the attached structures such as the hilum, ureter, bladder abdominal aorta and the inferior vena cava were noted and recorded. Results: Out of the 50 cadavers that were included into the study, 5 of them had congenital renal anomaly accounting for 10% of the deaths due to renal failure in adults. All the patients were between 40–60 years of age. There were two cases of lobulated kidney, one horse – shoe shaped kidney, one case of congenital hypoplasia and one 7 shaped left kidney. Conclusion: Renal anomalies are one of the common congenital anomalies which may remain unnoticed till adulthood. Of them, renal agenesis, horseshoe kidneys, renal hypoplasia and lobulated kidneys are relatively predominant. Keywords: Congenital renal anomalies, Cadavers, renal hypoplasia, Lobulated kidney, Horseshoe kidney. Introduction Hypoplasia usually occurs due to inadequate Congenital abnormalities of the kidneys and ureteral bud branching and results in a small kidney urinary tract play a major role in the morbidity and with histologically normal nephrons, though few in mortality.
    [Show full text]
  • 16 the Kidney J
    16 The Kidney J. Charles Jennette FPO FPO FPO FPO CONGENITAL ANOMALIES IgA Nephropathy (Berger Disease) Renal Agenesis Anti-Glomerular Basement Membrane Ectopic Kidney Glomerulonephritis Horseshoe Kidney ANCA Glomerulonephritis Renal Dysplasia VASCULAR DISEASES CONGENITAL POLYCYSTIC KIDNEY DISEASES Renal Vasculitis Autosomal Dominant Polycystic Kidney Disease Hypertensive Nephrosclerosis (Benign Nephrosclerosis) (ADPKD) Malignant Hypertensive Nephropathy Autosomal Recessive Polycystic Kidney Disease Renovascular Hypertension (ARPKD) Thrombotic Microangiopathy Nephronophthisis–Medullary Cystic Disease Cortical Necrosis ACQUIRED CYSTIC KIDNEY DISEASE DISEASES OF TUBULES AND INTERSTITIUM GLOMERULAR DISEASES Acute Tubular Necrosis (ATN) Nephrotic Syndrome Pyelonephritis Nephritic Syndrome Analgesic Nephropathy Glomerular Inflammation and Immune Mechanisms Drug-Induced (Hypersensitivity) Acute Tubulointerstitial Minimal-Change Glomerulopathy Nephritis Focal Segmental Glomerulosclerosis (FSGS) Light-Chain Cast Nephropathy Membranous Glomerulopathy Urate Nephropathy Diabetic Glomerulosclerosis RENAL STONES (NEPHROLITHIASIS AND Amyloidosis UROLITHIASIS) Hereditary Nephritis (Alport Syndrome) OBSTRUCTIVE UROPATHY AND HYDRONEPHROSIS Thin Glomerular Basement Membrane Nephropathy RENAL TRANSPLANTATION Acute Postinfectious Glomerulonephritis MALIGNANT TUMORS OF THE KIDNEY Type I Membranoproliferative Glomerulonephritis Wilms’ Tumor (Nephroblastoma) Type II Membranoproliferative Glomerulonephritis Renal Cell Carcinoma (RCC) (Dense Deposit Disease)
    [Show full text]
  • Congenital Anomalies of Kidney and Ureter
    ogy: iol Cu ys r h re P n t & R y e s Anatomy & Physiology: Current m e o a t Mittal et al., Anat Physiol 2016, 6:1 r a c n h A Research DOI: 10.4172/2161-0940.1000190 ISSN: 2161-0940 Review Article Open Access Congenital Anomalies of Kidney and Ureter Mittal MK1, Sureka B1, Mittal A2, Sinha M1, Thukral BB1 and Mehta V3* 1Department of Radiodiagnosis, Safdarjung Hospital, India 2Department of Paediatrics, Safdarjung Hospital, India 3Department of Anatomy, Safdarjung Hospital, India Abstract The kidney is a common site for congenital anomalies which may be responsible for considerable morbidity among young patients. Radiological investigations play a central role in diagnosing these anomalies with the screening ultrasonography being commonly used as a preliminary diagnostic study. Intravenous urography can be used to specifically identify an area of obstruction and to determine the presence of duplex collecting systems and a ureterocele. Computed tomography and magnetic resonance (MR) imaging are unsuitable for general screening but provide superb anatomic detail and added diagnostic specificity. A sound knowledge of the anatomical details and familiarity with these anomalies is essential for correct diagnosis and appropriate management so as to avoid the high rate of morbidity associated with these malformations. Keywords: Kidney; Ureter; Intravenous urography; Duplex a separate ureter is seen then the supernumerary kidney is located cranially in relation to the normal kidney. In such a case the ureter Introduction enters the bladder ectopically and according to the Weigert-R Meyer Congenital anomalies of the kidney and ureter are a significant cause rule the ureter may insert medially and inferiorly into the bladder [2].
    [Show full text]
  • UNILATERAL MEDULLARY SPONGE KIDNEY FIG. 1 Multiple Right
    Case Report doi: 10.22374/jeleu.v1i1.12 UNILATERAL MEDULLARY SPONGE KIDNEY Rodrigo Neira S, Diego Barrera C, Gastón Astroza E Facultad de Medicina, Pontifi cia Universidad Católica de Chile, Santiago, Chile. Corresponding Author Gastón Astroza E, MD: gaeulufi @gmail.com Submitted: May 15, 2018. Accepted: July 5, 2018. Published: August 21, 2018. ABSTRACT A 40-year-old female with an allergy to medium contrast, presented with bilateral loin pain and renal colic type radiation. Image study with non-contrast computerized tomography and magnetic resonance imaging revealed multiple nephrolithiasis and a complex cyst at lower pole of the right kidney and no findings in the left one. The patient was treated with laser lithotripsy by flexible ureterorenoscopy revealing multiple lithiasis within cystic dilatations of the urothelium. The complex cyst was submitted to partial nephrec- tomy. Finally, biopsy revealed renal parenchyma with polycystic changes in the external corticomedullary area. All findings were compatible with unilateral medullary sponge kidney diagnosis. CLINICAL CASE A 40-year-old female patient presented with a his- tory of insulin resistance (treated with metformin), allergy to contrast medium, and maternal urolithia- sis. The patient consulted for bilateral loin pain and right renal colic pain. Non-contrast computerized tomography (NCCT) (Figures 1 and 2) demonstrated multiple right nephrolithiasis and a 3-cm hypodense right lower pole lesion with some calcifications. This was diagnosed as a complex cyst. Related to this cyst, a magnetic resonance imaging (MRI) of the abdo- men was requested which showed a 3.5 cm Bosniak 3 right renal cyst. Resolution of the lithiasis was decided by means of flexible ureterorenoscopy (fURS) with laser lithotripsy.
    [Show full text]
  • Polycystic Horseshoe Kidney with Ruptured Stanford Type B Aortic Dissection
    doi: 1053.446/actamednicomedia.944563 Cilt: 4 Sayı: 2 Haziran 2021 / Vol: 4 Issue: 2 June 2021 https://dergipark.org.tr/tr/pub/actamednicomedia Case Report | Olgu Sunumu POLYCYSTIC HORSESHOE KIDNEY WITH RUPTURED STANFORD TYPE B AORTIC DISSECTION POLİKİSTİK ATNALI BÖBREK İLE BİRLİKTE GÖRÜLEN RÜPTÜRE STANDFORD TİP B AORTİK DİSEKSİYON Özgür Çakır1 , Zeki Talas2, Demet Doğan3* 1Kocaeli University, School of Medicine, Departmant of Radiology, Kocaeli, Turkey. 2Kocaeli University, School of Medicine, Department of Cardiovascular Surgery, Kocaeli, Turkey. 3Tuzla State Hospital, Radiology, İstanbul, Turkey. ABSTRACT ÖZ 60-year-old male patient presented to the emergency clinic At nalı böbrek genellikle asemptomatiktir; ancak enfeksiyon, complaining of nausea, vomiting and abdominal pain with no üreter taşları ve malignite gibi nedenlerle semptomatik hale remarkable medical history except hypertension and active gelebilir. Literatürde, yetişkin polikistik böbrek hastalığı ile ilişkili smoking. The computed tomography (CT) revealed a Stanford B- eşzamanlı durumlar arasında karaciğerde yaygın kistik lezyonlar, type aortic dissection starting from the thoracic aorta to the iliac kolon divertikülü, kapak kalp hastalığı ve serebral arter anevrizması arteries and polycystic horseshoe kidneys with multiple cysts in the yer alır. Hipertansiyon ve aktif sigara içimi dışında kayda değer bir liver. Since polycystic horseshoe kidney and Stanford type B tıbbi öyküsü olmayan, 60 yaşında erkek hasta, bulantı, kusma ve dissection of the thoracic aorta is rare, and no study showing karın ağrısı şikayetleri ile acil polikliniğe başvurdu. Yapılan coexistence in the literature was found. This is the first case report Bilgisayarlı tomografi (BT) incelemede; torasik aorttan iliak that reveals the association of these clinical findings and CT images arterlere uzanım gösteren Standford tip B diseksiyon ve eşlik eden in literature.
    [Show full text]
  • Ultrasound Appearance of Congenital Renal Disease: Pictorial Review
    The Egyptian Journal of Radiology and Nuclear Medicine (2014) 45, 1255–1264 Egyptian Society of Radiology and Nuclear Medicine The Egyptian Journal of Radiology and Nuclear Medicine www.elsevier.com/locate/ejrnm www.sciencedirect.com REVIEW Ultrasound appearance of congenital renal disease: Pictorial review Narrotam A. Patel, Pokhraj P. Suthar * Department of Radiology, S.S.G. Hospital, Medical College, Vadodara, India Received 12 April 2014; accepted 27 June 2014 Available online 5 August 2014 KEYWORDS Abstract Congenital renal diseases consist of a variety of entities. The age of presentation and GUT; clinical examination narrow down the differential diagnosis; however, imaging is essential for accu- Renal disease; rate diagnosis and pretreatment planning. Ultrasound is often used for initial evaluation. Computed Congenital; tomography (CT) and MRI provide additional information. Ultrasonography continues to occupy Ultrasonography a central role in the evaluation and detection of congenital renal diseases due to its advantage of rapid scanning time, lack of radiation exposure, cost effective and easy feasibility. Ó 2014 The Egyptian Society of Radiology and Nuclear Medicine. Production and hosting by Elsevier B.V. Open access under CC BY-NC-ND license. Contents 1. Technique. 1256 1.1. Anomalies related to ascent of kidney. 1256 1.1.1. Ectopia . 1256 1.1.2. Crossed renal ectopia . 1256 1.1.3. Horseshoe kidney. 1257 1.2. Anomalies related to the ureteric bud . 1258 1.2.1. Renal agenesis . 1258 1.2.2. Supernumerary kidney . 1258 1.2.3. Duplex collecting system and ureterocele . 1258 1.2.4. Uretero-pelvic junction obstruction . 1259 1.2.5. Congenital megacalyces .
    [Show full text]
  • Urinary System Birth Defects in Surgically Treated Infants in Sarajevo &Region of Bosnia and Herzegovina
    URINARY SYSTEM BIRTH DEFECTS IN SURGICALLY TREATED INFANTS IN SARAJEVO &REGION OF BOSNIA AND HERZEGOVINA Selma Aličelebić*, Dina Kapić, Zakira Mornjaković Institute of Histology and Embryology, University of Sarajevo, Faculty of Medicine, Čekaluša , Sarajevo, Bosnia and Herzegovina * Corresponding author Abstract Congenital anomalies of the urinary system are relatively common anomalies. In Bosnia and Herzegovi- na there is no existent unique evidence of congenital anomalies and registries. Th e aim of this study was to obtain the frequency of diff erent urinary tract anomalies types and their sex distribution among cases hospitalized in the Department of Pediatric Surgery of the University of Sarajevo Clinics Centre, Bosnia and Herzegovina, during the period from January to December . Retrospective study was car- ried out on the basis of clinical records. Standard methods of descriptive statistics were performed for the data analysis. Among patients that were surgically treated , of the patients were male patients, while , were female patients. Twenty nine diff erent urinary system anomalies types were found in this study. Th ese were: vesicoureteral refl ux ( cases or ,), hypospadias ( cases or ,), pelvi- ureteric junction obstruction ( cases or ,), megaureter ( cases or ,), duplex pelvis and ure- ter ( cases or ,), bladder diverticulum ( cases or ,), ureterocoele ( cases or ,), stenosis of the external urethral opening ( cases or ,), ectopic kidney, duplex kidney and pelvis (each cases or ,), polycystic kidneys and urethral stricture (each cases or ,), multicystic kidney ( cases or ,), kidney agenesis, ureter agenesis, urethral diverticulum, ectopic ureter, horseshoe kidney and fetal kidney (each cases or ,), renal aplasia, urethral atresia, renal cyst, urachal cyst, epispadias, bladder exstrophy, renal hypoplasia, renal malrotation and Prune-Belly syndrome (each case or ,).
    [Show full text]
  • Congenital Segmental Giant Megaureter Presenting As Cystic
    ical C lin as C e f R o Paonam and Bag, J Clin Case Rep 2015, 5:10 l e a p n o r r DOI: 10.4172/2165-7920.1000614 t u s o J Journal of Clinical Case Reports ISSN: 2165-7920 Case Report Open Access Congenital Segmental Giant Megaureter Presenting as Cystic Abdominal Mass in a Child Somorendro Paonam* and Sananda Bag Max Superspeciality Hospitals, Mohali, Punjab, India Abstract A six years old male child presented with gradually progressive distension of abdomen since one year of his age. Imaging suggested it as a large mesenteric cyst. Further evaluation and intra-operative findings suggested it to be bilateral congenital megaureter with giant one on the left side which was causing gross abdominal distension. Excision of left megaureteric segment, psoas hitch and ureteroneocystostomy was performed. Excision, tapering and uretereroneocystostomy of right ureter was performed. Congenital giant megaureter should be considered as one of differential diagnosis in children presenting as abdominal mass. Keywords: Giant megaureter; Renal descensus; Ureteroneocystos- well with normal renal function and no recurrence of distension of tomy; Psoas hitch; Abdominal mass abdomen. CECT scan shows bilateral enhancing kidneys (Figure 3a) with excretion of contrast in bilateral ureters (Figure 3b). Introduction Discussion Megaureter is a generic term indicating the presence of an enlarged ureter with or without concomitant dilatation of the upper collecting Megaureter is a spora¬dic or familial disease, where males are system. The normal diameter of ureter is usually 5 mm in children and more commonly affected than females and the commonest cause is rarely exceeds this size.
    [Show full text]
  • Renal Transplantation in a Patient with Polycystic Horseshoe Kidney - Case Report
    Central Journal of Clinical Nephrology and Research Bringing Excellence in Open Access Case Report *Corresponding author Luis Alberto Batista Peres, Department of Nephrology, State University of Western Parana, Street Vicente Machado, 2355, Paraná, Brazil, Tel: 55 Renal Transplantation in 45 30388010; Email: Submitted: 11 July 2017 a Patient with Polycystic Accepted: 10 August 2017 Published: 19 August 2017 Horseshoe Kidney - Case Report ISSN: 2379-0652 Copyright Francilayne Moretto dos Santos1, Luis Alberto Batista Peres2*, and © 2017 Batista Peres et al. 3 José Roberto Leonel Ferreira OPEN ACCESS 1FAG University Center, Brazil 2Department of Nephrology, State University of Western Parana, Brazil Keywords 3Department of Radiology, State University of Western Parana, Brazil • Horseshoe kidney • Polycystic kidney disease • Transplantion Abstract • Graftsurvival Polycystic horseshoe kidney is a very rare occurrence. A 47-year-old woman patient was admitted to hospital complaining of increased belly volume. Familial history was positive for horseshoe kidney and polycystic kidney. Computerized tomography showed enlarged kidneys with multiple cysts, fused by their lower poles and multiple liver cysts. She remained on dialysis for four years, being submitted to kidney transplantation with a related live donor, presenting normal renal function after nineteen months of follow up. INTRODUCTION found, with perdition for the male gender and occurring about 0.25% of the population [2,3]. It is usually asymptomatic, but the Horseshoe kidney results of an anomaly fusion during affected individuals are more prone to a variety of complications embryogenesis, while the polycystic kidney is an autosomal such as renal lithiasis, ureteropelvic junction stenosis, dominant hereditary disorder. It is a very rare occurrence found renovascular hypertension, polycystic kidneys and polycystic both anomalies in the same patient.
    [Show full text]
  • Horseshoe Kidney
    Rev. Colomb. Nefrol. 2017;4(2): 217 - 225 http://www.revistanefrologia.org Case report doi: http://dx.doi.org/10.22265/acnef.4.2.278 Horseshoe Kidney Riñón en herradura Catalina Vásquez-Guarín1, Frank Rojo-González2, Juan Ríos-Salazar3,*, Karen Ruiz-Naranjo3, Jineth Carolina Sarmiento-Rodríguez3 1Northwest Regional Pathology Group, Anthropology and Forensic Identification, National Institute of Legal Medicine and Forensic Sciences, Medellín, Colombia. 2Forensic Assistant, National Institute of Legal Medicine, Medellín, Colombia. 3Student, Medicine Program, School of Health Sciences, Corporación Universitaria Remington, Medellín, Colombia. Abstract We present the clinical case of a 39 year old male that presented with a violent death in the city of Medellin. During the necropsy, a horses- hoe Kidney was found, which was never diagnosed according to the patients’ medical history. It is a case relevant in the medical field given the unusual vasculature that was found, because it’s not a usual arrangement. The lack of symptoms and its spontaneous finding during the necropsy, shows us that it’s not a rare find in our environment and that it has a big impact in the surgical fields, and in occasions, with urinary tract infections. Methodology: Descriptive. Informed consent was given by the deceased relatives for the use and analysis of the medical history. Key words: Anatomic variant, horseshoe kidney, renal, kidney, renal blood flow, renal function, anastomosis. doi: http://dx.doi.org/10.22265/acnef.4.2.278 Resumen Se expone el caso de un hombre de 39 años que presenta muerte violenta en la ciudad de Medellín. Durante la necropsia se encuentra un riñón en herradura, que no tuvo diagnóstico clínico en su momento, según los hallazgos en su historial médico.
    [Show full text]
  • The Comparison of the Incidence of Horseshoe Kidney in Autopsy Cases Versus Urologic Patient Population
    Okajimas Folia Anat. Jpn., 76(2-3): 137-140. August, 1999 The Comparison of the Incidence of Horseshoe Kidney in Autopsy Cases Versus Urologic Patient Population By Halil BASAR, Ruhgun BASAR, M. Murat BASAR and Mine ERBIL Assistant Professor in Department of Urology, Faculty of Medicine, Kirikkale University, Kirikkale, Turkey Associate Professor in Department of Anatomy, Faculty of Medicine, Hacettepe University, Ankara, Turkey Urologist in Ankara Numune Hospital, 1st Urology Clinic, Ankara, Turkey Assistant Professor in Department of Anatomy , Faculty of Medicine, Hacettepe University, Ankara, Turkey -Received for Publication, February 15, 1999- Key Words: Horseshoe kidney, Urology, Anatomy, Autopsy Summary: This study was applied on 9665 cases between January 1993 and October 1998. Of these, 6985 (72.3%) were urologic patients and 2680 (27.7%) were autopsy cases. The patients having urinary complaint investigated by urine analysis and kidney-ureter-bladder film (KUB), routinely. In all patients who have pathological urine, ultrasonography exam was done and in all patients who established an abnormality on ultrasonografy, intravenous pyelography (IVP) was taken, also. We established the horseshoe kidney in 23 of patients (1/304) and in 6 of autopsy cases (1/447) with overall inci- dence 1/333. There were 21 male and 8 female with horseshoe kidney (male/female = 2.6/1). Abdominal discomfort with lower lumbar pain and Rovsing's sign were seen in 56.5% and in 65.2% of patients respectively. We concluded that horseshoe kidney incidence is almost the same as reported in the literature, although its clinical appearance is higher in our urologic patient population. In the urological out-patient evaluation, at least Rovsing's sign should be applied to all patients with lower lumbar pain with vague abdominal discomfort and an abdominal ultra- sonographic exam should be applied, if this sign is positive.
    [Show full text]