Diagnostic Atlas of Renal Pathology, by Agnes B. Fogo, MD and Michael Kashgarian, MD, delivers practical, highly visual guidance for effectively and accurately diagnosing a wide range of pathologic entities. More than 700 high-quality illustrations help you to recognize the pathologic features and clinical manifestations of both common and rare renal disorders and to formulate confident and accurate diagnoses. Thoroughly updated throughout, this companion to Brenner & Rector's, The Kidney, 9th Edition provides the newest information regarding categorizing and classification of diseases and describes how this relates to the various morphological lesions illustrated and their clinical significance. Access the complete text and all of the illustrations at www.expertconsult.com.

Chapter 1 Glomerular Diseases


NORMAL GROWTH AND MATURATION


PRIMARY GLOMERULAR DISEASES


Glomerular Diseases that Cause Nephrotic Syndrome: Non-Immune Complex


Introduction

Minimal Change Disease

Focal Segmental Glomerulosclerosis

Collapsing Glomerulopathy

Tip Lesion Variant of FSGS

Cellular Variant of FSGS

Perihilar Variant of FSGS

Congenital Nephrotic Syndrome of Finnish Type

Diffuse Mesangial Sclerosis

Glomerular Diseases that Cause Nephrotic/Nephritic Syndrome: Complement-Related


C1q Nephropathy

Dense Deposit Disease

C3 Glomerulopathies

Glomerular Diseases that Cause Nephrotic Syndrome: Immune Complex


Membranous Nephropathy

Membranoproliferative Glomerulonephritis Type 1

Fibrillary Glomerulonephritis

Immunotactoid Glomerulopathy


Glomerular Diseasesthat Cause Hematuria or Nephritic Syndrome: Immune Complex

Acute Post-infectious Glomerulonephritis


IgA Nephropathy


SECONDARY GLOMERULAR DISEASES


Diseases Associated with Nephrotic Syndrome


Monoclonal Immunoglobulin Deposition Disease

Proliferative Glomerulonephritis with Monoclonal Immunoglobulin Deposition

HIV-associated Nephropathy

Sickle Cell Nephropathy

Fabry's Disease

Lipoprotein Glomerulopathy

Lecithin-Cholesterol Acyltransferase Deficiency

Hereditary FSGS

Diseases Associated with Nephritic Syndrome or RPGN: Immune-Mediated


Lupus Nephritis, Mesangial and Proliferative Types

Henoch-Sch¶nlein Purpura

Mixed Connective Tissue Disease

Mixed Cryoglobulinemic Glomerulonephritis

Anti-GBM-Antibody Mediated Glomerulonephritis

Diseases Associated with Nephritic Syndrome or RPGN: Pauci-Immune- or Non-Immune-Mediated


Introduction

Granulomatosis with Polyangiitis (Wegener's)/Microscopic Polyangiitis

Polyarteritis Nodosa

Churg-Strauss Syndrome

Diseases of the Basement Membrane


Alport Syndrome

Thin Basement Membrane Lesions

Nail-Patella Syndrome

Glomerular Involvement with Bacterial Infections

Subacute Bacterial Endocarditis Glomerulonephritis

Shunt Nephritis


Chapter 2 Vascular Diseases

Diabetic Nephropathy

Thrombotic Microangiopathy/Thrombotic Thrombocytopenic Purpura

Scleroderma (Progressive Systemic Sclerosis)

Anti-phospholipid Antibody Disease

Preeclampsia and Eclampsia


Fibromuscular Dysplasia


Arterionephrosclerosis


Accelerated/Malignant Hypertension


Atheroemboli


Chapter 3 Tubulointerstitial Diseases


Introduction

Acute Pyelonephritis

Chronic Pyelonephritis and Reflux Nephropathy

Xanthogranulomatous Pyelonephritis

Malakoplakia

Acute Tubulointerstitial Nephritis-Drug-Related

Acute Tubulointerstitial Nephritis--Viral Infection

Anti-Tubular Basement Membrane Antibody Nephritis

IgG4-Related Tubulointerstitial Nephritis

Sarcoidosis

Acute Kidney Injury/Acute Tubular Necrosis

Heavy Metal Nephropathy (Lead and Cadmium Nephropathy)

Analgesic Nephropathy and Papillary Necrosis

Light Chain Cast Nephropathy and Tubulopathy

Tubular Crystallopathies

Indinavir Nephropathy

Lithium Nephropathy

Aristolochic Acid Nephropathy

Chapter 4 Chronic Kidney Disease


Introduction

Age-Related Sclerosis

Glomerular vs. Tubulointerstitial vs. Vascular Disease


Segmental Glomerulosclerosis-Primary vs. Secondary


Chapter 5 Renal Transplantation

Introduction&' || 'nbsp;&' || 'nbsp;

Antibody-Mediated Rejection&' || 'nbsp;&' || 'nbsp;

Chronic Active Antibody-Mediated Rejection and Transplant Glomerulopathy

Acute T-Cell-Mediated Rejection

Chronic Allograft Failure (Chronic Allograft Nephropathy)

Cyclosporin/FK506 Nephrotoxicity&' || 'nbsp;&' || 'nbsp;

Post-Transplant Lymphoproliferative Disease&' || 'nbsp;&' || 'nbsp;

Viral Infections&' || 'nbsp;&' || 'nbsp;

Chapter 6 Cystic Diseases of the Kidney

&' || 'nbsp;

Introduction&' || 'nbsp;&' || 'nbsp;

Autosomal dominant polycystic kidney disease&' || 'nbsp;&' || 'nbsp;

Autosomal recessive polycystic kidney disease&' || 'nbsp;&' || 'nbsp;

Medullary cystic disease&' || 'nbsp;&' || 'nbsp;

Medullary sponge kidney&' || 'nbsp;&' || 'nbsp;

Acquired cystic disease&' || 'nbsp;&' || 'nbsp;

Cystic renal dysplasia&' || 'nbsp;&' || 'nbsp;

Chapter 7 Renal Neoplasia

&' || 'nbsp;

Introduction&' || 'nbsp;&' || 'nbsp;

Renal Cell Carcinomas&' || 'nbsp;&' || 'nbsp;

Other Renal Epithelial Tumors&' || 'nbsp;&' || 'nbsp;

Wilms' Tumor&' || 'nbsp;&' || 'nbsp;

Transitional Cell Carcinoma of the Renal Pelvis&' || 'nbsp;&' || 'nbsp;