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Author:   Robert B. Colvin (Benjamin Castleman Distinguished Professor of Pathology, Department of Pathology, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts) ,  Anthony Chang (Chief Intelligence and Innovation Officer (CIIO) and Medical Director, Heart Failure Program, Children's Hospital of Orange County, CA, USA)
Publisher:   Elsevier - Health Sciences Division
Imprint:   Elsevier - Health Sciences Division
Edition:   3rd edition
Weight:   3.470kg
ISBN:  

9780323661089

ISBN 10:   0323661084
Pages:   1176
Publication Date:   30 April 2019
Audience:   Professional and scholarly ,  Professional & Vocational
Replaced By:   9780443107177
Format:   Hardback
Publisher's Status:   Active
Availability:   Available To Order  
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Table of Contents

Introduction Introduction and Overview Introduction to Renal Pathology Normal Kidney Structure Normal Kidney Development Glomerular Diseases Podocytopathies Minimal Change Disease Classification of FSGS Etiologic Classification of FSGS FSGS, Primary FSGS, Adaptive (Secondary) Collapsing Glomerulopathy Membranous Glomerulonephritis Etiologic Classification of Membranous Glomerulonephritis Membranous Glomerulonephritis, Primary Membranous Glomerulonephritis, Secondary Membranous Glomerulonephritis With Anti-TBM Antibodies C3-Related Glomerulonephritis and Membranoproliferative Glomerulonephritis Classification of MPGN and Complement-Related Diseases Dense Deposit Disease C3 Glomerulonephritis Membranoproliferative Glomerulonephritis With Immune Complexes IgA-Related Glomerulonephritis Overview of IgA-Related Glomerulopathies IgA Nephropathy IgA Vasculitis (Henoch-Schoenlein Purpura) SLE and Related Autoantibody-Mediated GN Systemic Lupus Erythematosus Mixed Connective Tissue Disease Rheumatoid Arthritis Mixed Cryoglobulinemic Glomerulonephritis Idiopathic Nonlupus Full-House Nephropathy Anti-GBM Nephritis Anti-GBM Glomerulonephritis Atypical Anti-GBM Nephritis Monoclonal Immunoglobulin Diseases Introduction to Diseases With Monoclonal Immunoglobulin Deposits Monoclonal Immunoglobulin Deposition Disease Proliferative Glomerulonephritis With Monoclonal IgG Deposits Membranous Glomerulonephritis With Masked IgG ? Deposits Type I Cryoglobulinemic Glomerulonephritis Waldenstroem Macroglobulinemia Amyloidosis Amyloidosis Classification AL/AH Amyloidosis AA Amyloidosis AFib Amyloidosis AGel Amyloidosis ALECT2 Amyloidosis AApoAI Amyloidosis ApoAII Amyloidosis AApoAIV Amyloidosis AApoCII Amyloidosis ATTR Amyloidosis Idiopathic Fibrillary Glomerulopathies Diseases With Organized Deposits Fibrillary Glomerulopathy Immunotactoid Glomerulopathy Fibronectin Glomerulopathy Diabetic Renal Disease Diabetic Nephropathy Idiopathic Nodular Glomerulopathy Infection-Related Glomerular Disease Overview of Infection-Related Glomerular Disease Acute Poststreptococcal Glomerulonephritis Acute Postinfectious Glomerulonephritis, Nonstreptococcal IgA Acute Glomerulonephritis Associated With *Staphylococcus aureus* Glomerulonephritis of Chronic Infection, Including Shunt Nephritis Endocarditis Syphilis Lyme Disease Hepatitis B Virus Hepatitis C Virus HIV-Associated Nephropathy Miscellaneous HIV-Associated Renal Diseases Schistosomiasis Filariasis Leishmaniasis Drug Induced Glomerular Diseases Drug-Induced Minimal Change Disease Bisphosphonate-Induced Collapsing Glomerulopathy Chloroquine Toxicity Anti-Hepatitis C Virus Drugs Anti-EGFR Drugs Genetic Diseases of the Glomerulus Overview and Classification of Genetic Diseases of the Glomerulus Genetic Diseases of the Glomerular Basement Membrane Collagen Alport Syndrome Thin Basement Membrane Disease Genetic Diseases of the Podocyte Diffuse Mesangial Sclerosis Congenital Nephrotic Syndrome of the Finnish Type Pierson Syndrome Galloway-Mowat Syndrome Denys-Drash Syndrome Frasier Syndrome Podocin Deficiency Alpha-Actinin-4 Deficiency Autosomal Dominant FSGS Due to *INF2* Mutations *APOL1*-Related Glomerular Disease Schimke Immuno-Osseous Dysplasia Genetic Storage and Lipid Diseases Lecithin-Cholesterol Acyltransferase Deficiency APOE Lipoprotein Glomerulopathy Type III Hyperlipoproteinemia Fabry Disease Gaucher Glomerulopathy I-Cell Disease (Mucolipidosis II) Alagille Syndrome Other Genetic Diseases Affecting the Glomerulus Glomerulopathy of Hereditary Multiple Exostoses Type III Collagen Glomerulopathy Nail-Patella Syndrome Miscellaneous Glomerular Diseases C1q Nephropathy IgM Nephropathy Cryofibrinogenic Glomerulopathy Hepatic Glomerulosclerosis and IgA Deposition Hemophagocytic Glomerulopathy Podocyte Infolding Glomerulopathy Metabolic Syndrome/Obesity-Related Glomerular Disease Intravascular Large B-Cell Lymphoma Vascular Diseases Overview and Classification of Systemic Vasculitides ANCA Disease ANCA-Related Glomerulonephritis Microscopic Polyangiitis Granulomatosis With Polyangiitis Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) Drug-Induced ANCA Vasculitis Non-ANCA Vasculitides Polyarteritis Nodosa Kawasaki Disease Giant Cell Arteritis Takayasu Arteritis Hypocomplementemic Urticarial Vasculitis (Anti-C1q Vasculitis) Thrombotic Microangiopathies Introduction to Thrombotic Microangiopathies Hemolytic Uremic Syndrome, Infection Related Thrombotic Microangiopathy, Genetic Thrombotic Microangiopathy, Autoimmune Thrombotic Microangiopathy, Drug Induced Postpartum Hemolytic Uremic Syndrome Scleroderma Renal Disease Multicentric Castleman Disease Other Diseases Affecting the Endothelium Preeclampsia, Eclampsia, HELLP Syndrome Radiation Nephropathy Glomerulopathy of Hereditary Multiple Extoses Sickle Cell Nephropathy Hypertensive Renal Disease Hypertensive Renovascular Disease Renal Artery Stenosis Fibromuscular Dysplasia Neurofibromatosis Thrombotic and Embolic Disease Renal Vein Thrombosis Renal Artery Thrombosis Atheromatous Emboli Hydrophilic Polymer Emboli Tubulointerstitial Diseases Overview and Classification of Tubulointerstitial Diseases Differential Diagnosis of Acute Interstitial Nephritis Ischemic Injury Acute Tubular Injury Renal Cortical Necrosis Septicemia/Shock Bile Cast Nephropathy Immunologic Tubular Disease Tubulointerstitial Nephritis With Uveitis Sjoegren Syndrome IgG4-Related Kidney Disease Idiopathic Hypocomplementemic Tubulointerstitial Nephritis Anti-Tubular Basement Membrane Disease Antibrush Border Autoantibody Tubulointerstitial Nephritis Sarcoidosis Tubulointerstiital Nephritis with IgM+ Plasma Cells Giant Cell Tubulitis With TBM Deposits Monoclonal Immunoglobulin Diseases of Tubules Light Chain Cast Nephropathy Light Chain Proximal Tubulopathy With Crystals Light Chain Proximal Tubulopathy Without Crystals Drug-Induced Tubulointerstitial Diseases Drug-Induced Acute Interstitial Nephritis Drugs That Cause Tubulointerstitial Nephritis Checkpoint Inhibitor-Induced Kidney Diseases Papillary Necrosis Myoglobinuria/Rhabdomyolysis/Hemoglobinuria Cisplatin Nephrotoxicity Osmotic Tubulopathy Antiviral Drug Nephrotoxicity Acute Phosphate Nephropathy Lithium-Induced Renal Disease Calcineurin Inhibitor Toxicity mTOR Inhibitor Toxicity Vancomycin-Induced Cast Nephropathy Warfarin Nephropathy Illicit Drugs and Opioids Toxic Injury Lead and Other Heavy Metal Toxins Aristolochic Acid Nephropathy Balkan Endemic Nephropathy Ethylene Glycol Toxicity Argyria Autosomal Dominant Tubulointerstitial Kidney Disease Autosomal Dominant Tubulointerstitial Kidney Disease, *MUC1*-Related Autosomal Dominant Tubulointerstitial Kidney Disease, *UMOD*-Related Autosomal Dominant Tubulointerstitial Kidney Disease, *REN*-Related Autosomal Dominant Tubulointerstitial Kidney Disease, *HNF1B*-Related Genetic Crystal Depostion Diseases Primary Hyperoxaluria 2,8-Dihydroxyadeninuria Cystinosis Uric Acid Nephropathy/Gout Genetic Transport Diseases Bartter Syndrome Dent Disease Oculocerebrorenal Syndrome of Lowe Other Genetic Diseases Affecting Tubules Methylmalonic Acidemia Systemic Karyomegaly Mitochondriopathies Miscellaneous Tubulointerstitial Diseases Nephrocalcinosis Secondary Oxalosis Mesoamerican Nephropathy Extramedullary Hematopoiesis Infections of the Kidney Bacterial Infections of the Kidney Acute Pyelonephritis Chronic Pyelonephritis Xanthogranulomatous Pyelonephritis Malakoplakia Tuberculosis BCG Granulomatous Interstitial Nephritis Leprosy Megalocytic Interstitial Nephritis Nocardiosis Leptospirosis Whipple Disease Fungal, Rickettsial, and Parasitic Infections of the Kidney Mucormycosis Candidiasis Histoplasmosis Coccidioidomycosis Blastomycosis Paracoccidioidomycosis Aspergillosis Cryptococcosis Microsporidiosis Rickettsial Infections Toxoplasmosis Hydatidosis Viral Infections of the Kidney Polyomavirus Nephritis Cytomegalovirus Infection Adenovirus Infection Epstein-Barr Virus Nephritis Herpes Simplex Acute Nephritis Hantavirus Nephropathy Developmental Diseases Overview of Congenital Anomalies of the Kidney and Urinary Tract Dysplasia/Hypoplasia/Agenesis Oligomeganephronia Ectopia, Malrotation, Duplication, Fusion, Supernumerary Kidney Ask-Upmark Kidney Renal Tubular Dysgenesis Cystic Diseases Overview of Cystic Diseases Ciliopathies Autosomal Dominant Polycystic Kidney Disease Autosomal Recessive Polycystic Kidney Disease Nephronophthisis and Related Ciliopathies Other Genetic Cystic Diseases von Hippel-Lindau Disease Tuberous Sclerosis Complex Zellweger Syndrome Miscellaneous Cystic Diseases Medullary Sponge Kidney Mixed Epithelial and Stromal Tumor Family Pediatric Cystic Nephroma Acquired Cystic Disease Simple and Miscellaneous Cysts Renal Lymphangioma/Lymphangiectasia Diseases of the Collecting System Introduction to Impediments to Urine Flow Reflux Nephropathy Obstructive Nephropathy Nephrolithiasis Loin Pain Hematuria Syndrome Diseases of the Renal Allograft Pathologic Classification of Renal Allograft Diseases Introduction Evaluation of Allograft Kidney Evaluation of the Donor Kidney Rejection Acute T-Cell-Mediated Rejection Chronic T-Cell-Mediated Rejection Hyperacute Rejection Acute Antibody-Mediated Rejection Chronic Antibody-Mediated Rejection Transcript Analysis of Renal Transplant Biopsies Recurrent and De Novo Diseases Diseases That Recur in Allografts De Novo FSGS De Novo Membranous Glomerulonephritis Anti-GBM Disease in Alport Syndrome Engraftment Syndrome Nonimmunologic Injury Acute Allograft Ischemia Hyperperfusion Injury Urine Leak Lymphocele Transplant Renal Artery Stenosis Renal Artery or Vein Thrombosis Posttransplant Lymphoproliferative Disease BK Polyomavirus Neoplasia Stable and Accepted Grafts Protocol Biopsies Accommodation Tolerance Kidney Pathology in Recipients of Other Transplants Kidney Diseases in Nonrenal Transplant Recipients Graft-vs.-Host Glomerulopathies Protocols Biopsy Reports Kidney Needle Biopsy: Evaluation for Adequacy Evaluation of Fibrosis Immunofluorescence on Paraffin Tissue Sections EM Processing From Paraffin or Frozen Tissue Detection of PLA2R Deposits and Autoantibodies Alport Collagen IV Immunofluorescence C4d Immunohistochemistry/Immunofluorescence Polyomavirus Detection in Tissue Mass Spectrometry Diagnostic Genetics of Kidney Diseases Examination of the End-Stage Kidney Examination of Tumor Nephrectomy Specimens for Nonneoplastic Diseases Evaluation of the Transplant Nephrectomy Evaluation of Autopsy Kidneys

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Robert Colvin, MD is Pathologist in Chief, Emeritus, Mass General Hospital and the Benjamin Castleman Distinguished Professor of Pathology, Harvard Medical School. Anthony Chang, MD is a Professor, Department of Pathology, University of Chicago with a specialty in renal pathology. His research interests include the role of B and plasma cells in lupus nephritis and transplant rejection. He is on the editorial board of Laboratory Investigation and Archives of Pathology and Laboratory Medicine, and past president of both the Renal Pathology Society (2017) and Chicago Pathology Society (2011-2013). He has taught more than 30 educational courses at the annual meetings for the American Society Clinical Pathology, College of American Pathologists, US & Canadian Academy of Pathology, American Society of Nephrology, American College of Rheumatology, and American Urological Association.

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