Index. electron microscopy, 81 immunofluorescence microscopy, 80 light microscopy, 80 Amyloidosis clinical setting, 185 etiology/pathogenesis,

Size: px
Start display at page:

Download "Index. electron microscopy, 81 immunofluorescence microscopy, 80 light microscopy, 80 Amyloidosis clinical setting, 185 etiology/pathogenesis,"

Transcription

1 A Acute antibody-mediated rejection (Acute AMR) clinical features, 203 clinicopathologic correlations, 206 pathogenesis, light microscopy, Acute cellular rejection (ACR) clinical setting, 199 pathogenesis, electron microscopy, 202 immunofluorescence microscopy, 202 light microscopy, Acute humoral rejection. See Acute antibody- mediated rejection (Acute AMR) Acute interstitial nephritis (AIN) clinical setting, 155 clinicopathologic correlations, 158 etiology/pathogenesis, , Acute tubular necrosis (ATN) ischemic pathogenesis, 170, toxic, 171 Afferent arterioles, 3, 5 African American Study of Kidney Disease (AASK) trial, 128 Alcoholic Bouin s solution, 9 Alport syndrome clinical setting, 79 etiology/pathogenesis, electron microscopy, light microscopy, 80 Amyloidosis clinical setting, 185 etiology/pathogenesis, electron microscopy, 187, light microscopy, Angiotensin-converting enzyme inhibitors (ACEI), 76 Anti-glomerular basement membrane antibody, 15 Anti-glomerular basement membrane disease, 109 clinicopathologic correlations, electron microscopy, , 111 light microscopy, Antineutrophil cytoplasmic autoantibody (ANCA) disease, 108 clinical setting, 112 clinicopathologic correlations, etiology/pathogenesis, 116, Anti-vascular endothelial derived growth factor (VEGF) agents, 140 Apoptosis, 170 Arcuate arteries, 3 Arterionephrosclerosis clinical setting, etiology/pathogenesis, 128 electron microscopy, 128 immunofluorescence, 127 light microscopy, A.B. Fogo et al., Fundamentals of Renal Pathology, DOI / , Springer-Verlag Berlin Heidelberg

2 226 B Banff system, 199 Basket-weaving appearance, GBM, 81 Bence Jones cast nephropathy clinical setting, 175 pathogenesis, immunohistochemistry and electron microscopy, 177 light microscopy, Bence Jones proteinuria, 176 Benign familial hematuria. See Thin basement membrane abnormality Bowman s space, 4 C Calcineurin inhibitor toxicity (CIT) clinical setting, 217 diagnosis, acute tubulopathy, arteriolopathy, thrombotic microangiopathy, 219 Calyces, 4 C3 glomerulonephritis clinical setting, 31 etiology/pathogenesis, 41 electron microscopy, 36 37, light microscopy, 34, 35 Cholesterol emboli, Chronic antibody-mediated rejection (Chronic AMR) clinical setting, diagnosis, 212 pathogenesis, electron microscopy, light microscopy, Chronic humoral rejection. See Chronic antibody-mediated rejection (Chronic AMR) Chronic interstitial nephritis clinical setting, 161 etiology/pathogenesis, gross findings, light microscopy, Chronic pyelonephritis, 164 Circumferential cellular interposition, 32 Columns of Bertin, 3 4 Cortex, 3 5 C1q nephropathy, 54 Crescents, 13 Cryoglobulinemic vasculitis, 109 Cryo-plugs, in capillary lumina, 39, 40 Cyclosporin A (CsA), 217 D Decompensated arterionephrosclerosis, 126 Dense deposit disease (DDD) clinicopathologic correlations, 41 etiology/pathogenesis, electron microscopy, 36, light microscopy, 34 Diabetic nephropathy clinical setting, 143 etiology/pathogenesis, 150 glomerular classification, 149 pathologic classification, electron microscopy, 148, light microscopy, Diffuse diabetic glomerulosclerosis, Diffuse lupus nephritis, Diffuse segmental lesions, 94 Distal tubule, 8, E Electron microscopy acute cellular rejection, 202 acute postinfectious glomerulonephritis, 65 Alport syndrome, 81 amyloidosis, 187, 188 anti-glomerular basement membrane disease, 110 Bence Jones cast nephropathy, 177 C3 glomerulonephritis, 36 37, 39

3 chronic antibody-mediated rejection, dense deposit disease, 36, 38 diabetic nephropathy, 148, 149 FSGS, 50 immunoglobulin A nephropathy and vasculitis, light and heavy-chain-deposition disease, membranous nephropathy, minimal change disease, 50 MPGN, scleroderma, thin basement membrane, 83 thrombotic microangiopathy, Endarteritis, Endocapillary proliferation, 62, 101 Exudative glomerulonephritis, 62 F Fibrillary glomerulonephritis clinical correlations, clinical setting, 191, Focal lupus nephritis, Focal segmental glomerulosclerosis (FSGS) clinical setting, 45 clinicopathologic correlations, C1q nephropathy, 54 etiology/pathogenesis, 50 electron microscopy, light microscopy, secondary, 55 Foot process effacement, 13, 25 chronic AMR, 210 FSGS, 51, 54 MCD, 50 MPGN, 36 G Giant cell arteritis, 108 Glomerular hyalinization, 12 Glomerular hyalinosis, 146 Glomerular scarring, 12 Goodpasture s syndrome. See Anti-glomerular basement membrane disease 227 H Heavy-chain-deposition disease. See Light-chain-deposition disease Hemolytic uremic syndrome (HUS) characterization, 135 clinicopathologic correlations, etiology/pathogenesis, electron microscopy, light microscopy, Henoch-Schönlein purpura. See Immunoglobulin A (IgA) nephropathy and vasculitis Humoral immunity, AIN, 157 Hyaline droplets, 13 Hyalinosis, 45, 47, 146 Hyperacute rejection, 206, 207 Hypertension arterionephrosclerosis, cholesterol emboli, scleroderma, I Immune complex vasculitis, 109 Immunofluorescence microscopy acute antibody-mediated rejection, acute cellular rejection, 202 acute postinfectious glomerulonephritis, Alport syndrome, 80 amyloidosis, 187 anti-glomerular basement membrane disease, 110, 111 C3 glomerulonephritis, 36 chronic antibody-mediated rejection, dense deposit disease, diabetic nephropathy, focal segmental glomerulosclerosis, 49 immunoglobulin A nephropathy and vasculitis, light and heavy-chain-deposition disease, 181 membranous nephropathy, 23, 24 MPGN, 34, 35 thin basement membrane, 83 thrombotic microangiopathy, 137

4 228 Immunoglobulin A (IgA) nephropathy and vasculitis definition, 69 etiology/pathogenesis, 74 electron microscopy, light microscopy, Immunotactoid glomerulopathy, Interferon-α therapy, 41 Interlobular arteries, 3 5 Interlobular veins, 3 Interstitial capillaries, 3 K Kawasaki disease, 108, 118 KDIGO guidelines, 76 Kimmelstiel Wilson (K W) nodules, 145 L Large-vessel vasculitis, Late graft loss, Light-chain cast nephropathy, 176. See also Bence Jones cast nephropathy Light-chain-deposition disease characterization, 179 clinical setting, 179 etiology/pathogenesis, 182 electron microscopy, light microscopy, 180 Light microscopy acute antibody-mediated rejection, acute cellular rejection, acute postinfectious glomerulonephritis, Alport syndrome, 80 amyloidosis, anti-glomerular basement membrane disease, Bence Jones cast nephropathy, C3 glomerulonephritis, 34, 35 chronic antibody-mediated rejection, dense deposit disease, 34 diabetic nephropathy, FSGS cellular variant, 49 classification schema, FSGS variants, 48 collapsing variant, 47, 48 glomerular tip lesion, 47, 49 glomerulosclerosis, 45, 46 hyalinosis, 45, 47 immunoglobulin A nephropathy and vasculitis, light and heavy-chain-deposition disease, 180 membranous nephropathy, minimal change disease, 45, 46 MPGN, scleroderma, 130, 131 thrombotic microangiopathy, Loop of Henle, 8 Lupus glomerulonephritis, 69 Lupus nephritis active and chronic glomerular lesions, 91 challenges, characterization, 89 clinicopathologic correlations, etiology/pathogenesis, ISN/RPS classification, 89, 90 advanced sclerosing lupus nephritis, 98 diffuse lupus nephritis, focal lupus nephritis, lupus podocytopathy, 98 membranous lupus nephritis, mesangial lupus nephritis, 91, 92 tubulointerstitial lesions, vascular lesions, Lupus podocytopathy, 98 M Malakoplakia, 164 Medium-vessel vasculitis, 108 Membranoproliferative glomerulonephritis (MPGN) characterization, 31 clinicopathologic correlations, 41 etiology/pathogenesis, electron microscopy, , 35 light microscopy, Membranous lupus nephritis, Membranous nephropathy clinical setting, 21 clinicopathologic correlations, 27 28

5 etiology/pathogenesis, electron microscopy, , 24 light microscopy, Mesangial cells, 7, 13 Mesangial lupus nephritis, 91, 92 Mesangiocapillary glomerulonephritis. See Membranoproliferative glomerulonephritis (MPGN) Michaelis-Gutmann bodies, 164 Microscopic polyangiitis (MPA), 108, 114 Minimal change disease (MCD) clinical setting, 45 etiology/pathogenesis, electron microscopy, 50 light microscopy, 45, 46 Monoclonal immunoglobulin deposition disease (MIDD), 150. See also Light-chain-deposition disease MPGN. See Membranoproliferative glomerulonephritis (MPGN) Myeloma cast nephropathy. See Bence Jones cast nephropathy N Nonreplacement phenomenon, 168, 169 O Onion-skin pattern, in scleroderma, 130, 131 Oxford classification system, IgA nephropathy, 75 P Pauci-immune crescentic glomerulonephritis, 113 Pedicles, 4 Podocyte foot processes, 65 Polyarteritis nodosa, 108, Polyomavirus clinical setting, 220 pathogenesis, 222 electron microscopy, immunohistochemistry, light microscopy, 220, 221 Postinfectious glomerulonephritis, acute clinical setting, clinicopathologic correlations, 67 etiology/pathogenesis, 66 electron microscopy, light microscopy, Progressive systemic sclerosis, Proliferative glomerulonephritis, 12 R Recurrent renal disease, Reflux nephropathy, 161, Renal allograft biopsies, 197, 198 Renal anatomy afferent arterioles, 3, 5 arcuate arteries, 3 Bowman s space, 4 collecting system, 4 cortex, 3 5 glomeruli, 4 6 interlobular arteries, 3, 4 interlobular veins, 3 loop of Henle, 8 medulla, 3 4 pathology glomeruli, interstitium, 14 tubules, tissue examination, 8 11 Renal diseases, pathogenic mechanisms in glomerular immunologic, nonimmunologic, 16 tubular and interstitial injury, 16 vasculature, Renal veins, 3 S Scleroderma, Sclerosis, 12 definition, 45 progressive systemic, Size-selective barrier, 8 Slit-pore diaphragm, 4 229

6 230 Small-vessel vasculitis, Staining characteristics, renal structures, 9 Streptococcal pyogenic exotoxin B (SpeB), 66 Systemic lupus erythematosus (SLE). See Lupus nephritis T Tacrolimus, 217 Takayasu arteritis, 108 Tamm-Horsfall protein (THP), Thin basement membrane abnormality clinical setting, electron microscopy, 83 etiology/pathogenesis, Thrombotic microangiopathies (TMA). See Hemolytic uremic syndrome (HUS); Thrombotic thrombocytopenic purpura (TTP) Thrombotic microangiopathy (TMA), 31, 219 Thrombotic thrombocytopenic purpura (TTP) characterization, 135 clinicopathologic correlations, etiology/pathogenesis, electron microscopy, immunofluorescence microscopy, 137 light microscopy, Toxic acute tubular necrosis, 171 Tram-track appearance, MPGN, 31 Transmural endarteritis, 201 Tubulointerstitial injury, 16 Tubulointerstitial lesions, Tubulointerstitial nephritis with uveitis (TINU) syndrome, 158 Tubuloreticular inclusions (TRIs), 97 U Uromodulin, V Verotoxin, W Wegener s granulomatosis, 108, 113, 115 Wire-loop lesions, 95, 97

Glomerular pathology in systemic disease

Glomerular pathology in systemic disease Glomerular pathology in systemic disease Lecture outline Lupus nephritis Diabetic nephropathy Glomerulonephritis Associated with Bacterial Endocarditis and Other Systemic Infections Henoch-Schonlein Purpura

More information

Glomerular diseases mostly presenting with Nephritic syndrome

Glomerular diseases mostly presenting with Nephritic syndrome Glomerular diseases mostly presenting with Nephritic syndrome 1 The Nephritic Syndrome Pathogenesis: proliferation of the cells in glomeruli & leukocytic infiltrate Injured capillary walls escape of RBCs

More information

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust Dr Ian Roberts Oxford Oxford Pathology Course 2010 for FRCPath Plan of attack: Diagnostic approach to the renal biopsy Differential diagnosis of the clinical syndromes of renal disease Microscopy Step

More information

Year 2004 Paper one: Questions supplied by Megan

Year 2004 Paper one: Questions supplied by Megan QUESTION 53 Endothelial cell pathology on renal biopsy is most characteristic of which one of the following diagnoses? A. Pre-eclampsia B. Haemolytic uraemic syndrome C. Lupus nephritis D. Immunoglobulin

More information

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust

Dr Ian Roberts Oxford. Oxford Pathology Course 2010 for FRCPath Illustration-Cellular Pathology. Oxford Radcliffe NHS Trust Dr Ian Roberts Oxford Oxford Pathology Course 2010 for FRCPath Present the basic diagnostic features of the commonest conditions causing proteinuria & haematuria Highlight diagnostic pitfalls Nephrotic

More information

Dr Ian Roberts Oxford

Dr Ian Roberts Oxford Dr Ian Roberts Oxford Oxford Pathology Course 2010 for FRCPath Present the basic diagnostic features of the commonest conditions causing renal failure Highlight diagnostic pitfalls. Crescentic GN: renal

More information

Histopathology: Glomerulonephritis and other renal pathology

Histopathology: Glomerulonephritis and other renal pathology Histopathology: Glomerulonephritis and other renal pathology These presentations are to help you identify basic histopathological features. They do not contain the additional factual information that you

More information

ESRD Dialysis Prevalence - One Year Statistics

ESRD Dialysis Prevalence - One Year Statistics Age Group IL Other Total 00-04 12 1 13 05-09 5 2 7 10-14 15 1 16 15-19 55 2 57 20-24 170 10 180 25-29 269 14 283 30-34 381 9 390 35-39 583 14 597 40-44 871 20 891 45-49 1,119 20 1,139 50-54 1,505 35 1,540

More information

Renal Pathology 1: Glomerulus. With many thanks to Elizabeth Angus PhD for EM photographs

Renal Pathology 1: Glomerulus. With many thanks to Elizabeth Angus PhD for EM photographs Renal Pathology 1: Glomerulus With many thanks to Elizabeth Angus PhD for EM photographs Anatomy of the Kidney http://www.yalemedicalgroup.org/stw/page.asp?pageid=stw028980 The Nephron http://www.beltina.org/health-dictionary/nephron-function-kidney-definition.html

More information

Glomerular pathology-2 Nephritic syndrome. Dr. Nisreen Abu Shahin

Glomerular pathology-2 Nephritic syndrome. Dr. Nisreen Abu Shahin Glomerular pathology-2 Nephritic syndrome Dr. Nisreen Abu Shahin 1 The Nephritic Syndrome Pathogenesis: inflammation proliferation of the cells in glomeruli & leukocytic infiltrate Injured capillary walls

More information

Surgical Pathology Report

Surgical Pathology Report Louisiana State University Health Sciences Center Department of Pathology Shreveport, Louisiana Accession #: Collected: Received: Reported: 6/1/2012 09:18 6/2/2012 09:02 6/2/2012 Patient Name: Med. Rec.

More information

Membranoproliferative Glomerulonephritis

Membranoproliferative Glomerulonephritis Membranoproliferative Glomerulonephritis MPGN is characterizedby alterations in the GBM and mesangium and by proliferation of glomerular cells. 5% to 10% of cases of 1ry nephrotic syndrome in children

More information

Clinical and pathological characteristics of patients with glomerular diseases at a university teaching hospital: 5-year prospective review

Clinical and pathological characteristics of patients with glomerular diseases at a university teaching hospital: 5-year prospective review Clinical and pathological characteristics of patients with glomerular diseases at a university teaching hospital: 5-year prospective review KW Chan, TM Chan, IKP Cheng Objective. To examine the prevalence

More information

PATTERNS OF RENAL INJURY

PATTERNS OF RENAL INJURY PATTERNS OF RENAL INJURY Normal glomerulus podocyte Glomerular capillaries electron micrograph THE CLINICAL SYNDROMES 1. The Nephrotic Syndrome 2. The Acute Nephritic Syndrome 3. Rapidly Progressive Glomerulonephritis

More information

A clinical syndrome, composed mainly of:

A clinical syndrome, composed mainly of: Nephritic syndrome We will discuss: 1)Nephritic syndrome: -Acute postinfectious (poststreptococcal) GN -IgA nephropathy -Hereditary nephritis 2)Rapidly progressive GN (RPGN) A clinical syndrome, composed

More information

RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT

RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT HISTOPATHOLOGIC DISORDERS AFFECTING THE ALLOGRAFT OTHER THAN REJECTION RECURRENT DISEASE DE NOVO DISEASE TRANSPLANT GLOMERULOPATHY Glomerular Non-glomerular

More information

29 Glomerular disease: an overview

29 Glomerular disease: an overview 29 Glomerular : an overview Renal Extra-renal Neurological changes Clinical syndromes pressure Sore throat (streptococcal) Rash Cardiac valve lesions Hemoptysis Asymptomatic or Acute Glomerulonephritis

More information

RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT. J. H. Helderman,MD,FACP,FAST

RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT. J. H. Helderman,MD,FACP,FAST RECURRENT AND DE NOVO RENAL DISEASES IN THE ALLOGRAFT J. H. Helderman,MD,FACP,FAST Vanderbilt University Medical Center Professor of Medicine, Pathology and Immunology Medical Director, Vanderbilt Transplant

More information

Mayo Clinic/ RPS Consensus Report on Classification, Diagnosis, and Reporting of Glomerulonephritis

Mayo Clinic/ RPS Consensus Report on Classification, Diagnosis, and Reporting of Glomerulonephritis Mayo Clinic/ RPS Consensus Report on Classification, Diagnosis, and Reporting of Glomerulonephritis Sanjeev Sethi, MD, PhD Department of Laboratory Medicine and Pathology Disclosure Relevant Financial

More information

Disorders of the kidney. Urine analysis. Nephrotic and nephritic syndrome.

Disorders of the kidney. Urine analysis. Nephrotic and nephritic syndrome. Disorders of the kidney. Urine analysis. Nephrotic and nephritic syndrome. Azotemia and Urinary Abnormalities Disturbances in urine volume oliguria, anuria, polyuria Abnormalities of urine sediment red

More information

Ordering Physician. Collected REVISED REPORT. Performed. IgG IF, Renal MCR. Lambda IF, Renal MCR. C1q IF, Renal. MCR Albumin IF, Renal MCR

Ordering Physician. Collected REVISED REPORT. Performed. IgG IF, Renal MCR. Lambda IF, Renal MCR. C1q IF, Renal. MCR Albumin IF, Renal MCR RenalPath Level IV Wet Ts IgA I Renal IgM I Renal Kappa I Renal Renal Bx Electron Microscopy IgG I Renal Lambda I Renal C1q I Renal C3 I Renal Albumin I Renal ibrinogen I Renal Mayo Clinic Dept. of Lab

More information

Approach to Glomerular Diseases: Clinical Presentation Nephrotic Syndrome Nephritis

Approach to Glomerular Diseases: Clinical Presentation Nephrotic Syndrome Nephritis GLOMERULONEPHRITIDES Vivette D Agati Jai Radhakrishnan Approach to Glomerular Diseases: Clinical Presentation Nephrotic Syndrome Nephritis Heavy Proteinuria Renal failure Low serum Albumin Hypertension

More information

Glomerulonephritis. Dr Rodney Itaki Anatomical Pathology Discipline.

Glomerulonephritis. Dr Rodney Itaki Anatomical Pathology Discipline. Glomerulonephritis Dr Rodney Itaki Anatomical Pathology Discipline. University of Papua New Guinea School of Medicine & Health Sciences Division of Pathology Gross anatomy Ref: Goggle Images Microanatomy

More information

Vasculitis (Polyarteritis Nodosa, Microscopic Polyangiitis, Wegener s Granulomatosis, Henoch- Schönlein Purpura)

Vasculitis (Polyarteritis Nodosa, Microscopic Polyangiitis, Wegener s Granulomatosis, Henoch- Schönlein Purpura) Vasculitis (Polyarteritis Nodosa, Microscopic Polyangiitis, Wegener s Granulomatosis, Henoch- Schönlein Purpura) J. Charles Jennette Ronald J. Falk The kidneys are affected by a variety of systemic vasculitides

More information

Fundamentals of Renal Pathology

Fundamentals of Renal Pathology Fundamentals of Renal Pathology Fundamentals of Renal Pathology Agnes B. Fogo, Arthur H. Cohen, J. Charles Jennette, Jan A. Bruijn, Robert B. Colvin Agnes B. Fogo, M.D. Vanderbilt University Medical Center

More information

Overview of glomerular diseases

Overview of glomerular diseases Overview of glomerular diseases *Endothelial cells are fenestrated each fenestra: 70-100nm in diameter Contractile, capable of proliferation, makes ECM & releases mediators *Glomerular basement membrane

More information

RaDaR Inclusion and Exclusion Criteria. Diagnosis Inclusion Criteria Exclusion Criteria. Alport Syndrome definite or probable

RaDaR Inclusion and Exclusion Criteria. Diagnosis Inclusion Criteria Exclusion Criteria. Alport Syndrome definite or probable Alport Syndrome and Type IV collagenopathies APRT Deficiency Alport Syndrome definite or probable Alport carrier definite or probable Thin basement membrane nephropathy APRT Deficiency confirmed Abolished

More information

2014 /2018 ERA-EDTA PRD Code ERA-EDTA PRD code 1996 ERA-EDTA. SNOMED CT concept identifier Convert ERA-EDTA Primary Renal Diagnosis (PRD) Term

2014 /2018 ERA-EDTA PRD Code ERA-EDTA PRD code 1996 ERA-EDTA. SNOMED CT concept identifier Convert ERA-EDTA Primary Renal Diagnosis (PRD) Term Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis 3380 901.1.C 90 Acute kidney injury Acute Renal Failure 14669001 Miscellaneous renal disorders 3398 901.2.C 90 Acute kidney injury due to hypovolaemia

More information

Pathology of Kidney Allograft Dysfunction. B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary

Pathology of Kidney Allograft Dysfunction. B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary Pathology of Kidney Allograft Dysfunction B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary The renal biopsy is a powerful tool in the diagnostic evaluation of allograft dysfunction

More information

Glomerular Pathology- 1 Nephrotic Syndrome. Dr. Nisreen Abu Shahin

Glomerular Pathology- 1 Nephrotic Syndrome. Dr. Nisreen Abu Shahin Glomerular Pathology- 1 Nephrotic Syndrome Dr. Nisreen Abu Shahin The Nephrotic Syndrome a clinical complex resulting from glomerular disease & includes the following: (1) massive proteinuria (3.5 gm /day

More information

Monoclonal Gammopathies and the Kidney. Tibor Nádasdy, MD The Ohio State University, Columbus, OH

Monoclonal Gammopathies and the Kidney. Tibor Nádasdy, MD The Ohio State University, Columbus, OH Monoclonal Gammopathies and the Kidney Tibor Nádasdy, MD The Ohio State University, Columbus, OH Monoclonal gammopathy of renal significance (MGRS) Biopsies at OSU (n=475) between 2007 and 2016 AL or AH

More information

DIABETES MELLITUS. Kidney in systemic diseases. Slower the progression: Pathology: Patients with diabetes mellitus are prone to other renal diseases:

DIABETES MELLITUS. Kidney in systemic diseases. Slower the progression: Pathology: Patients with diabetes mellitus are prone to other renal diseases: Kidney in systemic diseases Dr. Badri Paudel The kidneys may be directly involved in a number of multisystem diseases or secondarily affected by diseases of other organs. Involvement may be at a prerenal,

More information

Interpretation of Renal Transplant Biopsy. Arthur H. Cohen Wake Forest University School of Medicine Winston-Salem, North Carolina USA

Interpretation of Renal Transplant Biopsy. Arthur H. Cohen Wake Forest University School of Medicine Winston-Salem, North Carolina USA Interpretation of Renal Transplant Biopsy Arthur H. Cohen Wake Forest University School of Medicine Winston-Salem, North Carolina USA Renal Transplant Biopsies Tissue Processing Ideal world process as

More information

Case 3. ACCME/Disclosure. Laboratory results. Clinical history 4/13/2016

Case 3. ACCME/Disclosure. Laboratory results. Clinical history 4/13/2016 Case 3 Lynn D. Cornell, M.D. Mayo Clinic, Rochester, MN Cornell.Lynn@mayo.edu USCAP Renal Case Conference March 13, 2016 ACCME/Disclosure Dr. Cornell has nothing to disclose Clinical history 57-year-old

More information

NEPHRITIC SYNDROME. By Dr Mai inbiek

NEPHRITIC SYNDROME. By Dr Mai inbiek NEPHRITIC SYNDROME By Dr Mai inbiek Nephritic Syndrome The nephritic Syndrome is a clinical complex, usually of acute onset. Is caused by inflammatory lesions of glomeruli. Characterized by; 1) Hematuria

More information

C1q nephropathy the Diverse Disease

C1q nephropathy the Diverse Disease C1q nephropathy the Diverse Disease Danica Galešić Ljubanović School of Medicine, University of Zagreb Dubrava University Hospital Zagreb, Croatia Definition Dominant or codominant ( 2+), mesangial staining

More information

ERA-EDTA ERA-EDTA Primary Renal Diagnosis (PRD) Term ERA-EDTA PRD classification SNOMED CT PRD Code 1/1/2015

ERA-EDTA ERA-EDTA Primary Renal Diagnosis (PRD) Term ERA-EDTA PRD classification SNOMED CT PRD Code 1/1/2015 1003 Adult nephrotic syndrome - no histology Immunological Glomerulopathy 52254009 1019 Nephrotic syndrome of childhood - steroid sensitive - no histology Immunological Glomerulopathy 445119005 1026 Congenital

More information

RaDaR Inclusion and Exclusion Criteria. Diagnosis Inclusion Criteria Exclusion Criteria. Alport Syndrome definite or probable

RaDaR Inclusion and Exclusion Criteria. Diagnosis Inclusion Criteria Exclusion Criteria. Alport Syndrome definite or probable Alport Syndrome and Type IV collagenopathies APRT Deficiency Alport Syndrome definite or probable Alport carrier definite or probable Thin basement membrane nephropathy APRT Deficiency confirmed Abolished

More information

substance staining with IgG, C3 and IgA (trace) Linear deposition of IgG(+), IgA.M(trace) and C3(+++) at the DEJ

substance staining with IgG, C3 and IgA (trace) Linear deposition of IgG(+), IgA.M(trace) and C3(+++) at the DEJ Direct Immunofluorescence: Skin Diagnosis Findings Picture Pemphigus Vulgaris and it s Intracellular cement variants substance staining with IgG, C3 and IgA (trace) Bullous Pemphigoid and it s variants

More information

Glomerular Diseases. Anna Vinnikova, MD Nephrology

Glomerular Diseases. Anna Vinnikova, MD Nephrology Glomerular Diseases Anna Vinnikova, MD Nephrology Classification of Glomerular Diseases http://what-when-how.com/acp-medicine/glomerular-diseases-part-1/ Classification of pathologic and clinical manifestations

More information

Crescentic Glomerulonephritis (RPGN)

Crescentic Glomerulonephritis (RPGN) Crescentic Glomerulonephritis (RPGN) Background Rapidly progressive glomerulonephritis (RPGN) is defined as any glomerular disease characterized by extensive crescents (usually >50%) as the principal histologic

More information

Section Title. Subject Index

Section Title. Subject Index Section Title Subject Index Acute kidney injury definitions 287 289 hypoxia 287, 290 overview 286, 287 sublethal tubular injury adaptive responses 292, 293 combination of sublethal injuries 291, 292 detection

More information

Some renal vascular disorders

Some renal vascular disorders Some renal vascular disorders Introduction Nearly all diseases of the kidney involve the renal blood vessels secondarily We will discuss: -Hypertension (arterionephrosclerosis in benign HTN & hyperplastic

More information

RENAL EVENING SPECIALTY CONFERENCE

RENAL EVENING SPECIALTY CONFERENCE RENAL EVENING SPECIALTY CONFERENCE Harsharan K. Singh, MD The University of North Carolina at Chapel Hill Disclosure of Relevant Financial Relationships No conflicts of interest to disclose. CLINICAL HISTORY

More information

Case # 2 3/27/2017. Disclosure of Relevant Financial Relationships. Clinical history. Clinical history. Laboratory findings

Case # 2 3/27/2017. Disclosure of Relevant Financial Relationships. Clinical history. Clinical history. Laboratory findings Case # 2 Christopher Larsen, MD Arkana Laboratories Disclosure of Relevant Financial Relationships USCAP requires that all planners (Education Committee) in a position to influence or control the content

More information

GLOMERULAR TUBULAR/INTERSTITIAL BLOOD VESSELS

GLOMERULAR TUBULAR/INTERSTITIAL BLOOD VESSELS KIDNEY RENAL PATHOLOGY NORMAL CONGENITAL CYSTS GLOMERULAR TUBULAR/INTERSTITIAL BLOOD VESSELS OBSTRUCTION TUMORS 1. Renal Vein 2. Renal Artery 3. Renal Calyx 4. Medullary Pyramid 5. Renal Cortex 6. Segmental

More information

Nephritic vs. Nephrotic Syndrome

Nephritic vs. Nephrotic Syndrome Page 1 of 18 Nephritic vs. Nephrotic Syndrome Terminology: Glomerulus: A network of blood capillaries contained within the cuplike end (Bowman s capsule) of a nephron. Glomerular filtration rate: The rate

More information

Many patients receiving renal allografts become identified simply

Many patients receiving renal allografts become identified simply Recurrent Disease in the Transplanted Kidney Jeremy B. Levy Many patients receiving renal allografts become identified simply as recipients of kidney transplantation. All subsequent events involving changes

More information

Pathology of Complement Mediated Renal Disease

Pathology of Complement Mediated Renal Disease Pathology of Complement Mediated Renal Disease Mariam Priya Alexander, MD Associate Professor of Pathology GN Symposium Hong Kong Society of Nephrology July 8 th, 2017 2017 MFMER slide-1 The complement

More information

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus Mark Haas MD, PhD Department of Pathology & Laboratory Medicine Cedars-Sinai Medical

More information

RENAL BIOPSIES in patients with the clinical

RENAL BIOPSIES in patients with the clinical RENAL BIOPSY TEACHING CASE Crescentic Glomerulonephritis With a Paucity of Glomerular Immunoglobulin Localization Alexis A. Harris, MD, Ronald J. Falk, MD, and J. Charles Jennette, MD RENAL BIOPSIES in

More information

RENAL HISTOPATHOLOGY

RENAL HISTOPATHOLOGY RENAL HISTOPATHOLOGY Peter McCue, M.D. Department of Pathology, Anatomy & Cell Biology Sidney Kimmel Medical College There are no conflicts of interest. 1 Goals and Objectives! Goals Provide introduction

More information

RaDaR Inclusion and Exclusion Criteria

RaDaR Inclusion and Exclusion Criteria Cohort Inclusion Criteria Exclusion Criteria Adenine Phosphoribosyltransferase Deficiency (APRT-D) APRT Deficiency APRT Deficiency confirmed Abolished APRT enzyme activity or confirmed disease-causing

More information

Immune complex deposits in ANCA-associated crescentic glomerulonephritis: A study of 126 cases

Immune complex deposits in ANCA-associated crescentic glomerulonephritis: A study of 126 cases Kidney International, Vol. 65 (2004), pp. 2145 2152 Immune complex deposits in ANCA-associated crescentic glomerulonephritis: A study of 126 cases MARK HAAS and JOSEPH A. EUSTACE Department of Pathology

More information

Interesting case seminar: Native kidneys Case Report:

Interesting case seminar: Native kidneys Case Report: Interesting case seminar: Native kidneys Case Report: Proximal tubulopathy and light chain deposition disease presented as severe pulmonary hypertension with right-sided cardiac dysfunction and nephrotic

More information

Glomerular diseases with organized deposits

Glomerular diseases with organized deposits Glomerular diseases with organized deposits Banu Sis, MD, FRCPC University of Alberta, Edmonton, AB, Canada Ulusal Patoloji Kongresi, Manavgat, Antalya 8/11/2012 What is an organized deposit? A number

More information

CHAPTER 2. Primary Glomerulonephritis

CHAPTER 2. Primary Glomerulonephritis 2nd Report of the PRIMARY GLOMERULONEPHRITIS CHAPTER 2 Primary Glomerulonephritis Sunita Bavanandan Lee Han Wei Lim Soo Kun 21 PRIMARY GLOMERULONEPHRITIS 2nd Report of the 2.1 Introduction This chapter

More information

Renal Disease. Please refer to the assignment page Three online modules TBLs

Renal Disease. Please refer to the assignment page Three online modules TBLs Renal Disease Please refer to the assignment page Three online modules TBLs 1 Renal Embryology 2 Lab Tests UA CBC Enzymes Creatinine Creatinine clearance Ammonia Abs C Bx 3 BUN Creatinine Creatinine Clearance

More information

FIBRILLARY GLOMERULONEPHRITIS DIAGNOSTIC CRITERIA, PITFALLS, AND DIFFERENTIAL DIAGNOSIS

FIBRILLARY GLOMERULONEPHRITIS DIAGNOSTIC CRITERIA, PITFALLS, AND DIFFERENTIAL DIAGNOSIS FIBRILLARY GLOMERULONEPHRITIS DIAGNOSTIC CRITERIA, PITFALLS, AND DIFFERENTIAL DIAGNOSIS Guillermo A. Herrera MD Louisiana State University, Shreveport Fibrils in bundles 10-20 nm d Diabetic fibrillosis

More information

Dr Rodney Itaki Lecturer Anatomical Pathology Discipline. University of Papua New Guinea School of Medicine & Health Sciences Division of Pathology

Dr Rodney Itaki Lecturer Anatomical Pathology Discipline. University of Papua New Guinea School of Medicine & Health Sciences Division of Pathology Vasculitis Dr Rodney Itaki Lecturer Anatomical Pathology Discipline University of Papua New Guinea School of Medicine & Health Sciences Division of Pathology Disease Spectrum Hypersensitivity vasculitis/microscopic

More information

Pathology of Kidney Allograft Dysfunction. B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary

Pathology of Kidney Allograft Dysfunction. B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary Pathology of Kidney Allograft Dysfunction B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary The gold standard for exploration of the cause of an allograft dysfunction is to perform

More information

SCOTTISH REAL BIOPSY REGISTRY: SURVEY OF NATIVE KIDNEY BIOPSY IN SCOTLAND 2015

SCOTTISH REAL BIOPSY REGISTRY: SURVEY OF NATIVE KIDNEY BIOPSY IN SCOTLAND 2015 Scottish Renal Registry Report SECTION N SCOTTISH REAL BIOPSY REGISTRY: SURVEY OF NATIVE KIDNEY BIOPSY IN SCOTLAND All centres in Scotland were able to provide date of birth, sex (except centre), indication

More information

Primer: histopathology of calcineurin-inhibitor toxicity in renal allografts

Primer: histopathology of calcineurin-inhibitor toxicity in renal allografts Primer: histopathology of calcineurin-inhibitor toxicity in renal allografts Peter Liptak and Bela Ivanyi* SUMMARY Calcineurin inhibitors (ciclosporin and tacrolimus) can cause acute and chronic nephrotoxicity.

More information

Diabetic Nephropathy. Introduction/Clinical Setting. Pathologic Findings Light Microscopy. J. Charles Jennette

Diabetic Nephropathy. Introduction/Clinical Setting. Pathologic Findings Light Microscopy. J. Charles Jennette 12 Diabetic Nephropathy J. Charles Jennette Introduction/Clinical Setting Diabetic nephropathy is a clinical syndrome in a patient with diabetes mellitus that is characterized by persistent albuminuria,

More information

Mohammad Reza Shakibi M.D Kerman university of medical sciences (KMU) Shafa Hospital, Rheumatology ward

Mohammad Reza Shakibi M.D Kerman university of medical sciences (KMU) Shafa Hospital, Rheumatology ward VASCULITIS SYNDROMES Mohammad Reza Shakibi M.D Kerman university of medical sciences (KMU) Shafa Hospital, Rheumatology ward ILLUSTRATED CASE 1 A 56 years old lady refered me for prolonged fever, arthritis

More information

NEPHROTIC SYNDROME. Presents with the classic tetrad of nephrotic syndrome. Massive proteinuria (>3. 5 g/d) Hypoalbuminemia Edema Hyperlipidemia

NEPHROTIC SYNDROME. Presents with the classic tetrad of nephrotic syndrome. Massive proteinuria (>3. 5 g/d) Hypoalbuminemia Edema Hyperlipidemia PATHOLOGY OF GLOMERULAR DISEASES Disease Etiology Pathophysiology and Clinical Presentation Urinalysis in Nephrotic Syndrome NML excretion: 150 mg/d : < 0.15 g total protein/g urine creatinine Nephrosis

More information

29th Annual Meeting of the Glomerular Disease Collaborative Network

29th Annual Meeting of the Glomerular Disease Collaborative Network 29th Annual Meeting of the Glomerular Disease Collaborative Network Updates on the Pathogenesis IgA Nephropathy and IgA Vasculitis (HSP) J. Charles Jennette, M.D. Brinkhous Distinguished Professor and

More information

Dr. Rai Muhammad Asghar Head of Paediatric Department BBH Rawalpindi

Dr. Rai Muhammad Asghar Head of Paediatric Department BBH Rawalpindi Dr. Rai Muhammad Asghar Head of Paediatric Department BBH Rawalpindi Acute Post streptococcal Glomerulonephritis Sudden onset of Gross hematuria Edema Hypertension Renal insufficiency Cause of AGN Post

More information

An unusual association between focal segmental sclerosis and lupus nephritis: a distinct concept from lupus podocytopathy?

An unusual association between focal segmental sclerosis and lupus nephritis: a distinct concept from lupus podocytopathy? CEN Case Rep (2015) 4:70 75 DOI 10.1007/s13730-014-0142-1 CASE REPORT An unusual association between focal segmental sclerosis and lupus nephritis: a distinct concept from lupus podocytopathy? Hironari

More information

Case Presentation VASCULITIS. Case Presentation. Case Presentation. Vasculitis

Case Presentation VASCULITIS. Case Presentation. Case Presentation. Vasculitis Case Presentation VASCULITIS The patient is a 24 year old woman who presented to the emergency room with left-sided weakness. She was confused and complained of a severe headache. She was noted to have

More information

Diseases of the Kidney. Janos Vasko

Diseases of the Kidney. Janos Vasko Diseases of the Kidney Janos Vasko Congenital anomalies Glomerular diseases Tubulointerstitial diseases Infections Vascular diseases Stones Tumours POLYCYSTIC KIDNEY DISEASE INFANTILE TYPE ADULT TYPE Autosomal

More information

Case Presentation Turki Al-Hussain, MD

Case Presentation Turki Al-Hussain, MD Case Presentation Turki Al-Hussain, MD Director, Renal Pathology Chapter Saudi Society of Nephrology & Transplantation Consultant Nephropathologist & Urological Pathologist Department of Pathology & Laboratory

More information

Histopathology: Hypertension and diabetes in the kidney These presentations are to help you identify basic histopathological features.

Histopathology: Hypertension and diabetes in the kidney These presentations are to help you identify basic histopathological features. Histopathology: Hypertension and diabetes in the kidney These presentations are to help you identify basic histopathological features. They do not contain the additional factual information that you need

More information

ACUTE GLOMERULONEPHRITIS. IAP UG Teaching slides

ACUTE GLOMERULONEPHRITIS. IAP UG Teaching slides ACUTE GLOMERULONEPHRITIS 1 Definition Etiology Pathology/pathogenesis Risk factors Clinical Presentation Investigation Differential Diagnosis Management Outcome/Prognosis Indication for Renal Biopsy Summary

More information

VASCULITIS. Case Presentation. Case Presentation

VASCULITIS. Case Presentation. Case Presentation VASCULITIS Case Presentation The patient is a 24 year old woman who presented to the emergency room with left-sided weakness. She was confused and complained of a severe headache. She was noted to have

More information

GLOMERULONEPHRITIS BRRH Grand Rounds January 12, 2016

GLOMERULONEPHRITIS BRRH Grand Rounds January 12, 2016 GLOMERULONEPHRITIS BRRH Grand Rounds January 12, 2016 Wayne R. Kotzker, M.D. Renal Electrolyte & Hypertension Consultants of South Florida Affiliate Assistant Professor of Clinical Biomedical Sciences,

More information

Chapter 1. Incidence of End Stage Kidney Disease. Contents:

Chapter 1. Incidence of End Stage Kidney Disease. Contents: Chapter 1 Incidence of End Stage Kidney Disease Contents: Incidence of End Stage Kidney Disease 1-1 Stock and Flow 1-2 Incident patients 1-3 Incident Rates 1-3 Late Referral 1-7 Co-Morbidities 1-9 Primary

More information

Glomerular Diseases. Davis Massey, MD, PhD Surgical Pathology Anna Vinnikova, MD Nephrology

Glomerular Diseases. Davis Massey, MD, PhD Surgical Pathology Anna Vinnikova, MD Nephrology Glomerular Diseases Davis Massey, MD, PhD Surgical Pathology Anna Vinnikova, MD Nephrology Classification of Glomerular Diseases http://what-when-how.com/acp-medicine/glomerular-diseases-part-1/ Classification

More information

MLS Continuing Education Conference November PACE Session # Urinary Casts: The Importance of Laboratory Identification

MLS Continuing Education Conference November PACE Session # Urinary Casts: The Importance of Laboratory Identification MLS Continuing Education Conference November 2014 PACE Session # 304 113-14 Urinary Casts: The Importance of Laboratory Identification 1 Urinalysis The Beginning The field of laboratory medicine started

More information

Diabetes, Obesity and Heavy Proteinuria

Diabetes, Obesity and Heavy Proteinuria Diabetes, Obesity and Heavy Proteinuria Clinical Case 41 yo Black woman with heavy proteinuria History 2014: noted to have proteinuria on routine lab testing (1.1g/g). 1+ edema. Blood pressure has been

More information

GLOMERULONEPHRITIS CLINICAL APPROACH TO GLOMERULAR DISEASE ACOI 2018

GLOMERULONEPHRITIS CLINICAL APPROACH TO GLOMERULAR DISEASE ACOI 2018 GLOMERULONEPHRITIS CLINICAL APPROACH TO GLOMERULAR DISEASE ACOI 2018 Disclosures Nothing to declare Case 1 44 yo Caucasian woman admitted from PCP with dyspnea and HTN Has not felt well for 3-4 months

More information

CHAPTER 2 PRIMARY GLOMERULONEPHRITIS

CHAPTER 2 PRIMARY GLOMERULONEPHRITIS CHAPTER 2 Sunita Bavanandan Lim Soo Kun 19 5th Report of the 2.1: Introduction This chapter covers the main primary glomerulonephritis that were reported to the MRRB from the years 2005-2012. Minimal change

More information

Focal Segmental Glomerulosclerosis and the Nephro6c Syndrome Dr. A. Gangji Dr. P. Marge>s. Part 1: Clinical

Focal Segmental Glomerulosclerosis and the Nephro6c Syndrome Dr. A. Gangji Dr. P. Marge>s. Part 1: Clinical Focal Segmental Glomerulosclerosis and the Nephro6c Syndrome Dr. A. Gangji Dr. P. Marge>s Part 1: Clinical Pa#ent DM 18 year old McMaster student Back pain, severe fa#gue Oct 2006 Leg swelling to ER Nov

More information

PHGY210 Renal Physiology

PHGY210 Renal Physiology PHGY210 Renal Physiology Tomoko Takano, MD, PhD *Associate Professor of Medicine and Physiology McGill University *Nephrologist, McGill University Health Centre Lecture plan Lecture 1: Anatomy, basics

More information

The primary glomerulopathies are those disorders that affect

The primary glomerulopathies are those disorders that affect The Primary Glomerulopathies rthur H. Cohen Richard J. Glassock The primary glomerulopathies are those disorders that affect glomerular structure, function, or both in the absence of a multisystem disorder.

More information

CHAPTER 4. Paediatric Renal Biopsies

CHAPTER 4. Paediatric Renal Biopsies 2nd Report of the Malaysian Registry of Renal Biopsy 2008 PAEDIATRIC RENAL BIOPSIES CHAPTER 4 Paediatric Renal Biopsies Lee Ming Lee Lim Yam Ngo Lynster Liaw Susan Pee Wan Jazilah Wan Ismail Yap Yok Chin

More information

Case Presentation Turki Al-Hussain, MD

Case Presentation Turki Al-Hussain, MD Case Presentation Turki Al-Hussain, MD Director, Renal Pathology Chapter Saudi Society of Nephrology & Transplantation Consultant Nephropathologist & Urological Pathologist Department of Pathology & Laboratory

More information

Fußzeile (Titel der Präsentation) 1. Thrombotic Microangiopathy: The German Experience 4. Conflictof interest: none

Fußzeile (Titel der Präsentation) 1. Thrombotic Microangiopathy: The German Experience 4. Conflictof interest: none Thrombotic Microangiopathy: The German Experience 3 Nephropathology Section, Institute of Pathology, Hamburg, Germany Agenda 1. Difficulties in the diagnosis TMA 2. Previous efforts to reach consensus

More information

Redefining lupus nephritis: clinical implications of pathophysiologic subtypes

Redefining lupus nephritis: clinical implications of pathophysiologic subtypes Redefining lupus nephritis: clinical implications of pathophysiologic subtypes 1 Renal Division, Department of Medicine, Peking University First Hospital, Institute of Nephrology, Peking University, Key

More information

C3 GLOMERULOPATHIES. Budapest Nephrology School Zoltan Laszik

C3 GLOMERULOPATHIES. Budapest Nephrology School Zoltan Laszik C3 GLOMERULOPATHIES Budapest Nephrology School 8.30.2018. Zoltan Laszik 1 Learning Objectives Familiarize with the pathogenetic mechanisms of glomerular diseases Learn the pathologic landscape and clinical

More information

Chapter 8: ESRD Among Children, Adolescents, and Young Adults

Chapter 8: ESRD Among Children, Adolescents, and Young Adults Chapter 8: ESRD Among Children, Adolescents, and Young Adults The number of children beginning end-stage renal disease (ESRD) care decreased by 6% in 2014, totaling 1,398 (Figure 8.1.a). 9,721 children

More information

Diabetes on Renal Biopsy-Current Appraisal

Diabetes on Renal Biopsy-Current Appraisal Diabetes on Renal Biopsy-Current Appraisal Helen Liapis, M.D. Senior Consultant Arkana Labs Professor of Pathology & Immunology, retired Washington University School of Medicine St. Louis, MO BNS 2016

More information

glomerular capillary wall Pathogenic Mechanisms of Glomerular Diseases General Outline General Trend General Concepts

glomerular capillary wall Pathogenic Mechanisms of Glomerular Diseases General Outline General Trend General Concepts General Outline Pathogenic Mechanisms of Glomerular Diseases Patrick H. Nachman, MD Professor University of North Carolina UNC Kidney Center Chapel Hill, NC USA Overview of Pathogenetic Mechanisms For

More information

Elevated Serum Creatinine, a simplified approach

Elevated Serum Creatinine, a simplified approach Elevated Serum Creatinine, a simplified approach Primary Care Update Creighton University School of Medicine. April 27 th, 2018 Disclosure Slide I have no disclosures and have no conflicts with this presentation.

More information

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus

Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus Classification of Glomerular Diseases and Defining Individual Glomerular Lesions: Developing International Consensus Mark Haas MD, PhD Department of Pathology & Laboratory Medicine Cedars-Sinai Medical

More information

Biopsy Features of Kidney Allograft Rejection Banff B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary

Biopsy Features of Kidney Allograft Rejection Banff B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary Biopsy Features of Kidney Allograft Rejection Banff 2017 B. Ivanyi, MD Department of Pathology, University of Szeged, Szeged, Hungary Treatment of allograft dysfunction should rely on the biopsy findings

More information

Signs and symptoms of thin basement membrane nephropathy: A prospective regional study on primary glomerular disease The Limburg Renal Registry

Signs and symptoms of thin basement membrane nephropathy: A prospective regional study on primary glomerular disease The Limburg Renal Registry Kidney International, Vol. 66 (2004), pp. 909 913 Signs and symptoms of thin basement membrane nephropathy: A prospective regional study on primary glomerular disease The Limburg Renal Registry PIETER

More information

Patologie da attivazione del complemento G.F.Ferraccioli Istituto di Reumatologia e Scienze Affini Facolta di Medicina Universita Cattolica del sacro

Patologie da attivazione del complemento G.F.Ferraccioli Istituto di Reumatologia e Scienze Affini Facolta di Medicina Universita Cattolica del sacro Patologie da attivazione del complemento G.F.Ferraccioli Istituto di Reumatologia e Scienze Affini Facolta di Medicina Universita Cattolica del sacro Cuore Roma Roma 19.02.2016 TMA: complement disorders

More information

GLOMERULAR DISEASES. Dr. de Châtel Rudolf. Semmelweis Egyetem ÁOK, I.Sz.Belgyógyászati Klinika, Budapest

GLOMERULAR DISEASES. Dr. de Châtel Rudolf. Semmelweis Egyetem ÁOK, I.Sz.Belgyógyászati Klinika, Budapest GLOMERULAR DISEASES Dr. de Châtel Rudolf Semmelweis Egyetem ÁOK, I.Sz.Belgyógyászati Klinika, Budapest The CIBA Collection of Medical Illustrations Volume 6: Kidney, ureters and urinary bladder CIBA Medical

More information