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[Abdomen(GI)]Diagnostic Pathology: Kidney Diseases, 3e
 
정가  410,000원
판매가격  360,000
ISBN  9780323661089
출판사  Elsevier
저자  Colvin MD
발행일  2019-05-10
구매수량
 
 


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.
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

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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