Absolute renal biopsy diagnosis frequencies of the most common glomerular disease subtypes according to patient age category. Absolute renal biopsy diagnosis.

Slides:



Advertisements
Similar presentations
Immune Complex Nephritis.
Advertisements

Glomerular Diseases Dr. Atapour Differential diagnosis and evaluation of glomerular disease.
ISRTPCON and CME AIIMS NEW DELHI Sept,2013 Dr Kiran K Senior Resident, PDCC-Renal and Transplant Pathology Department of Histopathology PGIMER, Chandigarh.
Immune Complex Nephritis
Sulen Sarioglu, Mehtat Unlu, Mustafa Sakar, Taner Camsari, Mehmet Turkmen, Hulya Ellidokuz Departments of Pathology, Biomedical Technology, Nephrology,
Associate professor of Internal Medicine
1. Anatomy of kidney. 2. Parts of nephron 3. Kidney blood flow.
Kidney Lecture 1 – Normal, Function, Glomerulonephritis.
Clinico-pathological Analysis of Kidney Diseases in Children: A Retrospective, Single Center Study Dr. Bassam Saeed Pediatric Nephrologist Surgical Kidney.
Membranous-like Glomerulopathy with Masked IgG Kappa Deposits Chris Larsen, MD Renal Pathology Society Companion meeting, USCAP March 2016.
Disease Review: C3 Glomerulopathy
Associate professor of Internal Medicine
Figure 1 Schematic representation of idiopathic nephrotic syndrome,
Schematic diagram of a lobe of a normal glomerulus.
Table 1.2.1: Total number of renal biopsies by centres, 2005 – 2012
Immune Complex Nephritis
Volume 81, Issue 2, Pages (January 2012)
Important notes: Dear students…
Positive interactions between the basic and translational research, clinical research, patient care, and training components of an academic dialysis access.
Volume 93, Issue 3, Pages (March 2018)
Probability of cumulative incidence of ESRD, disease-related death, or death from other cause for the entire cohort. Probability of cumulative incidence.
Volume 75, Issue 9, Pages (May 2009)
Several microRNAs are differentially expressed in the glomeruli between different types of kidney disease. Several microRNAs are differentially expressed.
Overview of glomerular diseases
Distribution of Biopsy-Proven Presumed Primary Glomerulonephropathies in Among a Racially and Ethnically Diverse US Population  John J. Sim,
Volume 94, Issue 5, Pages (November 2018)
Nat. Rev. Nephrol. doi: /nrneph
Complement in Kidney Disease: Core Curriculum 2015
C3 glomerulopathy: what's in a name?
HIV-associated immune complex glomerulonephritis with “lupus-like” features: A clinicopathologic study of 14 cases1  Mark Haas, Sadhana Kaul, Joseph A.
Toward a working definition of C3 glomerulopathy by immunofluorescence
Complement in Kidney Disease: Core Curriculum 2015
Volume 76, Issue 5, Pages (September 2009)
Volume 61, Issue 1, Pages (January 2002)
HIV-related nephropathy: A South African perspective
Patient disposition. Patient disposition. AE, adverse event. *One patient died during the follow-up period. ^Four of the 12 discontinuations of treatment.
IgG4-related tubulointerstitial nephritis
Immunofluorescence on pronase-digested paraffin sections: A valuable salvage technique for renal biopsies  S.H. Nasr, S.J. Galgano, G.S. Markowitz, M.B.
Simplified diagrammatic representation of a selection of mechanisms of glomerular injury. Simplified diagrammatic representation of a selection of mechanisms.
The NEPTUNE Pathology Scoring System: Examples of descriptors.
Collapsing glomerulopathy.
Molecular defects in C regulation associated with C3 glomerulopathy and atypical hemolytic uremic syndrome. Molecular defects in C regulation associated.
Distribution of podocyte gene mutations in patients with genetic congenital nephrotic syndrome (CNS) and steroid–resistant nephrotic syndrome (SRNS). Distribution.
A glomerulus from a patient who developed nephrotic syndrome while receiving a nonsteroidal anti-inflammatory drug for arthritis. A glomerulus from a patient.
Transmission electron microscopy of a representative glomerular capillary enumerating pathologic changes associated with preeclampsia: 1, endothelial cell.
Conditions within the kidney that are conducive to C activation.
Glomerulus from a patient with primary membranous nephropathy showing the pathognomonic “spikes” of basement membrane projecting from the outer surface.
Pathogenesis of minimal change disease: hypotheses.
The risk of siblings being affected depends on the mode of inheritance and the gender of the affected parent (in X-linked disease). The risk of siblings.
Glomerular basement membrane (GBM) appearance and patterns of hearing loss in women with Alport syndrome. Glomerular basement membrane (GBM) appearance.
Unmasking a unique glomerular lesion
Response to cyclosporin A (CsA) treatment and renal outcome in patients with either nongenetic or genetic disease. Response to cyclosporin A (CsA) treatment.
These data are derived from 21,374 patients with any form of glomerular disease identified in renal biopsy specimens evaluated by the University of North.
Graph showing percentage of total patients with PTD or IGT that would be detected in each category of FBG if an oral glucose tolerance test were performed.
Representative electron microscopic image from a patient with SMGN
Mortality caused by cardiovascular disease (A) and sepsis (B) of patients with end-stage renal disease (ESRD) treated by dialysis compared with the general.
Relationship between time from diagnosis of type 2 diabetes to renal biopsy and the proportion of biopsies with any diabetic nephropathy (DN) and any non-diabetic.
Electron micrograph of chronic primary membranous nephropathy showing discontinuous, electron-dense deposits representing aggregates of PLA2R–anti-PLA2R.
Epidemiologic data of primary glomerular diseases in western France
Immunohistochemical and immunogluorescence analysis of renal biopsies showing significant C5b-9, C4d and C3c deposition but almost absent Bb deposition.
New dialysis starts in the United States by year in patients with and without diagnosis of diabetes. New dialysis starts in the United States by year in.
Collapsing glomerulopathy (CG) and lesions that may resemble CG histologically in renal biopsies from patients with systemic lupus erythematosus. Collapsing.
Renal biopsy specimen from a patient with IgA nephropathy and macroscopic hematuria–associated AKI. Light micrographs show mesangial proliferation, increased.
Incident cases of ESRD secondary to heroin-associated nephropathy, membranoproliferative glomerulonephritis type 1, HIV infection, and focal segmental.
Simplistic breakdown of the new MPGN classification using immunofluorescence as the basis and an approach to evaluation when the kidney biopsy indicated.
Monoclonal Ig deposition disease (MIDD) with diffuse and nodular glomerulosclerosis. Monoclonal Ig deposition disease (MIDD) with diffuse and nodular glomerulosclerosis.
Direct immunofluorescence showing granular mesangial staining for IgA in the expanded mesangium of the biopsy of patient 4, who had underlying diabetic.
Relative renal biopsy diagnosis frequencies of the most common glomerular disease subtypes according to patient age category and typical mode of clinical.
Dysproteinemia and the Kidney: Core Curriculum 2019
Thrombotic microangiopathies are classified into: Inherited or acquired primary; secondary; or infection associated TMAs. Current classifications define.
Presentation transcript:

Absolute renal biopsy diagnosis frequencies of the most common glomerular disease subtypes according to patient age category. Absolute renal biopsy diagnosis frequencies of the most common glomerular disease subtypes according to patient age category. (A) All subtypes: number of patients with each of the eight most common glomerular disease subtypes shown. (B) Nephrotic subtypes: number of patients with each of the eight most common glomerular disease subtypes that often present with nephrotic syndrome shown (Fabry disease and collagenofibrotic glomerulopathy not shown). (C) Nephritic subtypes: number of patients with each of the eight glomerular disease subtypes that often present clinically with nephritic features shown. DDD, dense deposit disease; GBM, glomerular basement membrane; GS, glomerulosclerosis; IgAN, IgA nephropathy; MIDD, monoclonal immune deposition disease; MPGN, membranoproliferative GN; TBM, thin basement membrane. Michelle M. O’Shaughnessy et al. CJASN 2017;12:614-623 ©2017 by American Society of Nephrology