Diagnostic Pathology: Kidney Diseases, 3/e

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  • Diagnostic Pathology: Kidney Diseases, 3/e 요약정보 및 구매

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    출판사 Elsevier
    저자명 Robert B. Colvin
    발행일 2019-05-06
    PAGE
    1176
    ISBN 9780323661089
    포인트 2,000P
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    • Diagnostic Pathology: Kidney Diseases, 3/e
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      Comprehensive and up to date, the third edition of Diagnostic Pathology: Kidney Diseases, written by Robert B. Colvin, MD and Anthony Chang, MD,expertly covers all aspects of common and rare renal diseases and their variants. This easy-to-use, point-of-care reference offers a state-of-the-art, concise presentation of major pathological, clinical, pathophysiological, and genetic information for more than 240 diagnoses, making it an ideal resource for pathologists and nephrologists to improve knowledge and skills. Significantly revised information throughout ensures that you remain current with everything new regarding the pathology and pathogenesis of nonneoplastic kidney diseases.


      Key Features 

      New content with over 20 new chapters covering idiopathic non-lupus full-house nephropathy, hemophagocytic glomerulonephritis, cryofibrinogenemic glomerulopathy, metabolic syndrome and obesity-related glomerular disease, Whipple disease, systemic Castleman disease, nephropathies due to direct acting antivirals for HCV, checkpoint inhibitors, EGFR antagonists, illicit drugs and opioids, Tums glomerulopathy, vancomycin-induced cast nephropathy, transcript analysis of renal biopsies, new forms of amyloidosis, and mass spectroscopyUpdated and validated pathologic classifications systems reflect details on new genetic, therapeutic, and pathologic information, including IgA nephropathy, lupus nephritis, vasculitis, and transplant pathologyMore than 3,300 outstanding, annotated images, including gross and microscopic pathology, a wide range of stains, and detailed medical illustrations, make this an invaluable diagnostic aid for every practicing pathologist, nephrologist, resident, or fellowTime-saving reference features include consistently templated chapters, bulleted text, a variety of test data tables, key facts in each chapter, annotated images, and an extensive indexInternationally recognized authors, many new to this edition, provide fresh perspectives on multiple topics, with a particular emphasis on practical information that directly assists in making and supporting a diagnosisEnhanced eBook version included with purchase, which allows you to access all of the text, figures, and references from the book on a variety of devices

      목차

      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-Schönlein 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 κ Deposits

      Type I Cryoglobulinemic Glomerulonephritis

      Waldenström 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

      Sjögren 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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