Having an Open Partial Nephrectomy
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The Risk of Tumour Recurrence in Patients Undergoing Renal
The Risk of Tumour Recurrence in Patients Undergoing Renal Transplantation for End-stage Renal Disease after Previous Treatment for a Urological Cancer: A Systematic Review Romain Boissier, Vital Hevia, Harman Max Bruins, Klemens Budde, Arnaldo Figueiredo, Enrique Lledó-García, Jonathon Olsburgh, Heinz Regele, Claire Fraser Taylor, Rhana Hassan Zakri, et al. To cite this version: Romain Boissier, Vital Hevia, Harman Max Bruins, Klemens Budde, Arnaldo Figueiredo, et al.. The Risk of Tumour Recurrence in Patients Undergoing Renal Transplantation for End-stage Renal Disease after Previous Treatment for a Urological Cancer: A Systematic Review. European Urology, Elsevier, 2018, pp.94 - 108. 10.1016/j.eururo.2017.07.017. hal-01792732 HAL Id: hal-01792732 https://hal-amu.archives-ouvertes.fr/hal-01792732 Submitted on 18 May 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 The risk of tumour recurrence in patients undergoing renal transplantation for end- stage renal disease after previous treatment for a urological cancer: a systematic review Romain Boissier1*, Vital Hevia2*, Harman Max Bruins3, Klemens Budde4, Arnaldo Figueiredo5, Enrique Lledó García6, Jonathon Olsburgh7, Heinz Regele8, Claire Fraser Taylor9, Rhana Hassan Zakri7, Cathy Yuhong Yuan10 and Alberto Breda11 * These authors contributed equally and share the first authorship 1. -
Wilms Tumour (Nephroblastoma) – Brief Information
Wilms Tumour (Nephroblastoma) – Brief information Copyright © 2017 Competence Network Paediatric Oncology and Haematology Author: Maria Yiallouros, created 2009/02/12, Editor: Maria Yiallouros, Release: Prof. Dr. med. Norbert Graf, English Translation: Dr. med. habil. Gesche Tallen, Last modified: 2017/06/27 Kinderkrebsinfo is sponsored by Deutsche Kinderkrebsstiftung Wilms Tumour (Nephroblastoma) – Brief information Page 2 Table of Content 1. General information on the disease ................................................................................... 3 2. Incidence .......................................................................................................................... 3 3. Causes ............................................................................................................................. 4 4. Symptoms ........................................................................................................................ 4 5. Diagnosis ......................................................................................................................... 4 5.1. Diagnostic imaging ....................................................................................................... 5 5.2. More tests to confirm diagnosis and to assess tumour spread (metastases) ..................... 5 5.3. Tests for preparing the treatment ................................................................................... 5 5.4. Obtaining a tumour sample (biopsy) ............................................................................. -
Partial Nephrectomy for Renal Cancer: Part I
REVIEW ARTICLE Partial nephrectomy for renal cancer: Part I BJUIBJU INTERNATIONAL Paul Russo Department of Surgery, Urology Service, and Weill Medical College, Cornell University, Memorial Sloan Kettering Cancer Center, New York, NY, USA INTRODUCTION The Problem of Kidney Cancer Kidney Cancer Is The Third Most Common Genitourinary Tumour With 57 760 New Cases And 12 980 Deaths Expected In 2009 [1]. There Are Currently Two Distinct Groups Of Patients With Kidney Cancer. The First Consists Of The Symptomatic, Large, Locally Advanced Tumours Often Presenting With Regional Adenopathy, Adrenal Invasion, And Extension Into The Renal Vein Or Inferior Vena Cava. Despite Radical Nephrectomy (Rn) In Conjunction With Regional Lymphadenectomy And Adrenalectomy, Progression To Distant Metastasis And Death From Disease Occurs In ≈30% Of These Patients. For Patients Presenting With Isolated Metastatic Disease, Metastasectomy In Carefully Selected Patients Has Been Associated With Long-term Survival [2]. For Patients With Diffuse Metastatic Disease And An Acceptable Performance Status, Cytoreductive Nephrectomy Might Add Several Additional Months Of Survival, As Opposed To Cytokine Therapy Alone, And Prepare Patients For Integrated Treatment, Now In Neoadjuvant And Adjuvant Clinical Trials, With The New Multitargeted Tyrosine Kinase Inhibitors (Sunitinib, Sorafenib) And Mtor Inhibitors (Temsirolimus, Everolimus) [3,4]. The second groups of patients with kidney overall survival. The explanation for this cancer are those with small renal tumours observation is not clear and could indicate (median tumour size <4 cm, T1a), often that aggressive surgical treatment of small incidentally discovered in asymptomatic renal masses in patients not in imminent patients during danger did not counterbalance a population imaging for of patients with increasingly virulent larger nonspecific abdominal tumours. -
What a Difference a Delay Makes! CT Urogram: a Pictorial Essay
Abdominal Radiology (2019) 44:3919–3934 https://doi.org/10.1007/s00261-019-02086-0 SPECIAL SECTION : UROTHELIAL DISEASE What a diference a delay makes! CT urogram: a pictorial essay Abraham Noorbakhsh1 · Lejla Aganovic1,2 · Noushin Vahdat1,2 · Soudabeh Fazeli1 · Romy Chung1 · Fiona Cassidy1,2 Published online: 18 June 2019 © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2019 Abstract Purpose The aim of this pictorial essay is to demonstrate several cases where the diagnosis would have been difcult or impossible without the excretory phase image of CT urography. Methods A brief discussion of CT urography technique and dose reduction is followed by several cases illustrating the utility of CT urography. Results CT urography has become the primary imaging modality for evaluation of hematuria, as well as in the staging and surveillance of urinary tract malignancies. CT urography includes a non-contrast phase and contrast-enhanced nephrographic and excretory (delayed) phases. While the three phases add to the diagnostic ability of CT urography, it also adds potential patient radiation dose. Several techniques including automatic exposure control, iterative reconstruction algorithms, higher noise tolerance, and split-bolus have been successfully used to mitigate dose. The excretory phase is timed such that the excreted contrast opacifes the urinary collecting system and allows for greater detection of flling defects or other abnormali- ties. Sixteen cases illustrating the utility of excretory phase imaging are reviewed. Conclusions Excretory phase imaging of CT urography can be an essential tool for detecting and appropriately characterizing urinary tract malignancies, renal papillary and medullary abnormalities, CT radiolucent stones, congenital abnormalities, certain chronic infammatory conditions, and perinephric collections. -
Wilms' Tumour (Nephroblastoma)
Wilms’ tumour (nephroblastoma) Wilms’ tumour is generally found only in children and very rarely in adults. JANET E POOLE, MB BCh, DCH (SA), FCP (SA) Paed Professor, Department of Paediatrics, Charlotte Maxeke Johannesburg Academic Hospital and University of the Witwatersrand, Johannesburg Janet Poole qualified as a medical doctor in 1978 at the University of the Witwatersrand and became a specialist paediatrician in 1983. She commenced work in the Paediatric Haematology/Oncology Unit at the Johannesburg Hospital in 1984 and has 25 years’ experience in that field. She was head of the Chris Hani Baragwanath Paediatric Haematology/Oncology Unit from 1989 to 1997, after which she became head of the Unit at Johannesburg Hospital. Her special interests are childhood leukaemia, Wilms’ tumour, and inherited haemoglobin defects. She has been involved with CHOC (a parent support group) since starting work in the unit. Correspondence to: J Poole ([email protected]) a bleeding diathesis, polycythaemia, weight loss, urinary infection, Epidemiology diarrhoea or constipation. Wilms’ tumour or nephroblastoma is a cancer of the kidney that The differential diagnosis of a renal mass includes hydronephrosis, typically occurs in children and very rarely in adults. The common polycystic kidney disease and infrequently xanthogranulomatous name is an eponym, referring to Dr Max Wilms, the German pyelonephritis. Non-renal peritoneal masses include neuroblastoma surgeon who first described this type of tumour in 1899. Wilms’ and teratoma (Fig. 1). tumour is the most common form of kidney cancer in children and is also known as nephroblastoma. Nephro means kidney, and a blastoma is a tumour of embryonic tissue that has not yet fully developed. -
Laparoscopic Nephrectomy
Laparoscopic Nephrectomy Information for Patients This leaflet explains: What is a Nephrectomy? ............................................................................................. 2 Why do I need a nephrectomy? ................................................................................... 3 What are the risks and side effects of laparoscopic nephrectomy? ............................. 3 Occasional risks ....................................................................................................... 3 Rare risks ................................................................................................................. 3 Very Rare Risks ....................................................................................................... 3 Before the operation .................................................................................................... 4 Day of your operation .................................................................................................. 4 How long will the operation take? ................................................................................ 4 After the operation ....................................................................................................... 4 Going home ................................................................................................................. 5 At home ....................................................................................................................... 5 Contacts ..................................................................................................................... -
(Pro)Renin Receptor (PRR) Expression in Renal Tumours
diagnostics Article Clinical Implications of (Pro)renin Receptor (PRR) Expression in Renal Tumours Jon Danel Solano-Iturri 1,2,3, Enrique Echevarría 4, Miguel Unda 5, Ana Loizaga-Iriarte 5, Amparo Pérez-Fernández 5, Javier C. Angulo 6, José I. López 3,7 and Gorka Larrinaga 3,4,8,* 1 Department of Pathology, Donostia University Hospital, 20014 Donostia/San Sebastian, Spain; [email protected] 2 Department of Medical-Surgical Specialities, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain 3 Biocruces-Bizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] 4 Department of Physiology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; [email protected] 5 Department of Urology, Basurto University Hospital, University of the Basque Country (UPV/EHU), 48013 Bilbao, Spain; [email protected] (M.U.); [email protected] (A.L.-I.); [email protected] (A.P.-F.) 6 Clinical Department. Faculty of Medical Sciences. European University of Madrid, 28905 Getafe, Spain; [email protected] 7 Department of Pathology, Cruces University Hospital, 48903 Barakaldo, Spain 8 Department of Nursing, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain * Correspondence: [email protected] Citation: Solano-Iturri, J.D.; Abstract: (1) Background: Renal cancer is one of the most frequent malignancies in Western countries, Echevarría, E.; Unda, M.; with an unpredictable clinical outcome, partly due to its high heterogeneity and the scarcity of Loizaga-Iriarte, A.; Pérez-Fernández, reliable biomarkers of tumour progression. -
Pyelography in Infants
Arch Dis Child: first published as 10.1136/adc.9.50.119 on 1 April 1934. Downloaded from PYELOGRAPHY IN INFANTS BY W. E. UNDERWOOD, F.R.C.S., Chief Assistant to a Surgical Unit, St. Bartholomew's Hospital. Pyelography in infants is an examination which is essential under certain circumstances, and from it valuable facts may often be obtained which would be undiscovered without this specialized form of investigation. Hitherto the examination has been surrounded by difficulties of such a nature that it is often unsuccessful and the child is submitted to discomfort without result. The object of this paper is to bring forward certain notes on cases where pyelography has been indicated. The observations from a series of sixteen cases have led to the development of a method whereby good pyelograms have been obtained with certainty. Instrumental pyelography in infancy is a procedure not to be advised lightheartedly, but there are occasions where the indications are definite and adequate: in these cases the anticipation of possible information to be gained justifies submitting the infants to what constitutes a major examination. In this series are cases of urinary infection resistant to the usual medical treatment, of renal pain, of renal calculi, and cases of congenital malformation http://adc.bmj.com/ of the urinary tract similar to those described by Poynton and Sheldon'. The term pyelography is used here for brevity rather than accuracy, for it embraces a complete investigation of the urinary tract, including ureterography. Methods of pyelography.-The choice lies between intravenous and on September 30, 2021 by guest. -
Neoplastic Metastases to the Endocrine Glands
27 1 Endocrine-Related A Angelousi et al. Metastases to endocrine 27:1 R1–R20 Cancer organs REVIEW Neoplastic metastases to the endocrine glands Anna Angelousi1, Krystallenia I Alexandraki2, George Kyriakopoulos3, Marina Tsoli2, Dimitrios Thomas2, Gregory Kaltsas2 and Ashley Grossman4,5,6 1Endocrine Unit, 1st Department of Internal Medicine, Laiko Hospital, National and Kapodistrian University of Athens, Athens, Greece 2Endocrine Unit, 1st Department of Propaedeutic Medicine, Laiko University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece 3Department of Pathology, General Hospital ‘Evangelismos’, Αthens, Greece 4Department of Endocrinology, OCDEM, University of Oxford, Oxford, UK 5Neuroendocrine Tumour Unit, Royal Free Hospital, London, UK 6Centre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK Correspondence should be addressed to A Angelousi: [email protected] Abstract Endocrine organs are metastatic targets for several primary cancers, either through Key Words direct extension from nearby tumour cells or dissemination via the venous, arterial and f glands lymphatic routes. Although any endocrine tissue can be affected, most clinically relevant f cancer metastases involve the pituitary and adrenal glands with the commonest manifestations f metastases being diabetes insipidus and adrenal insufficiency respectively. The most common f pituitary primary tumours metastasing to the adrenals include melanomas, breast and lung f adrenal carcinomas, which may lead to adrenal insufficiency in the presence of bilateral adrenal f thyroid involvement. Breast and lung cancers are the most common primaries metastasing to f ovaries the pituitary, leading to pituitary dysfunction in approximately 30% of cases. The thyroid gland can be affected by renal, colorectal, lung and breast carcinomas, and melanomas, but has rarely been associated with thyroid dysfunction. -
Tnm Frequently Asked Questions (Faq’S)
TNM FREQUENTLY ASKED QUESTIONS (FAQ’S) The TNM Project Committee receives questions concerning the use of TNM and how to interpret rules in specific situations. Some questions and answers are listed below by category for your convenience. These FAQs can th also be found in the TNM Supplement: a Commentary on Uniform Use, 4 Edition, 2012 (edited by Ch. Wittekind, C. Compton, J. Brierley, L. H. Sobin). Advice on further questions may be obtained from the TNM Helpdesk by accessing the TNM Classification of Malignant Tumours page at the UICC website www.uicc.org TABLE OF CONTENTS GENERAL QUESTIONS AJCC versus UICC TNM ................................................................................................................3 In situ carcinoma .............................................................................................................................3 Pathological Versus Clinical TNM ...................................................................................................3 When in Doubt ................................................................................................................................4 R Classification ...............................................................................................................................4 R Classification and Tis ..................................................................................................................5 Positive Cytology ............................................................................................................................5 -
Book of Courage and Hope
BOOK Kidney Cancer Patient Stories From Around OF The World COURAGE AND HOPE Introduction Thank you to the kidney cancer patients, Around the world, kidney cancer patients The IKCC “Book of Courage and Hope” also caregivers, and families who are featured so share a wide range of challenges – not only illustrates our belief that being a part of a beautifully throughout this “Book of Courage with different subtypes and stages of disease, cancer patient support group and sharing and Hope”. Sharing personal stories takes but often with inequitable and complex knowledge and experiences with each other tremendous courage. Each story is an amaz health systems in their home countries. The not only helps individual patients, but can ing testimony to the courage and unique determination of individual patients to push also serve more broadly to increase challenges faced by kidney cancer patients for better treatment options, to demand know ledge of unmet medical needs, raise and their caregivers. better care and support their fellow patients awareness, and foster further research in is truly remarkable. On behalf of the Inter kidney cancer. national Kidney Cancer Coalition (IKCC), we owe these patients and their families our deepest gratitude. 2 If there is an underlying theme that runs By publishing this book, the IKCC hopes to We welcome your feedback through most of our patient stories, it is one demonstrate the breadth and diversity of the on this publication: of fellowship and an innate understanding global kidney cancer community and, along [email protected] that it is often patients who are best motiva with our Affiliate Organisations, our shared Dr. -
Icd-9-Cm (2010)
ICD-9-CM (2010) PROCEDURE CODE LONG DESCRIPTION SHORT DESCRIPTION 0001 Therapeutic ultrasound of vessels of head and neck Ther ult head & neck ves 0002 Therapeutic ultrasound of heart Ther ultrasound of heart 0003 Therapeutic ultrasound of peripheral vascular vessels Ther ult peripheral ves 0009 Other therapeutic ultrasound Other therapeutic ultsnd 0010 Implantation of chemotherapeutic agent Implant chemothera agent 0011 Infusion of drotrecogin alfa (activated) Infus drotrecogin alfa 0012 Administration of inhaled nitric oxide Adm inhal nitric oxide 0013 Injection or infusion of nesiritide Inject/infus nesiritide 0014 Injection or infusion of oxazolidinone class of antibiotics Injection oxazolidinone 0015 High-dose infusion interleukin-2 [IL-2] High-dose infusion IL-2 0016 Pressurized treatment of venous bypass graft [conduit] with pharmaceutical substance Pressurized treat graft 0017 Infusion of vasopressor agent Infusion of vasopressor 0018 Infusion of immunosuppressive antibody therapy Infus immunosup antibody 0019 Disruption of blood brain barrier via infusion [BBBD] BBBD via infusion 0021 Intravascular imaging of extracranial cerebral vessels IVUS extracran cereb ves 0022 Intravascular imaging of intrathoracic vessels IVUS intrathoracic ves 0023 Intravascular imaging of peripheral vessels IVUS peripheral vessels 0024 Intravascular imaging of coronary vessels IVUS coronary vessels 0025 Intravascular imaging of renal vessels IVUS renal vessels 0028 Intravascular imaging, other specified vessel(s) Intravascul imaging NEC 0029 Intravascular