Unmasking a unique glomerular lesion

Slides:



Advertisements
Similar presentations
Membranous-like glomerulopathy with masked IgG kappa deposits
Advertisements

Mark A. Lusco, MD, Agnes B. Fogo, MD, Behzad Najafian, MD, Charles E
Volume 82, Issue 7, Pages (October 2012)
Agnes B. Fogo, MD, Mark A. Lusco, MD, Behzad Najafian, MD, Charles E
Volume 54, Issue 2, Pages (August 1998)
Myeloma-related Kidney Disease
Paraneoplastic glomerulopathies: New insights into an old entity
Hatem Elabd, Rushi Nayak, Tarek Rashid, M. Barry Stokes 
Sanjeev Sethi, Carla M. Nester, Richard J.H. Smith 
A 61-Year-Old Man With Membranoproliferative Glomerulonephritis
Histologic classification of glomerular diseases: clinicopathologic correlations, limitations exposed by validation studies, and suggestions for modification 
Agnes B. Fogo, MD, Mark A. Lusco, MD, Behzad Najafian, MD, Charles E
AJKD Atlas of Renal Pathology: Minimal Mesangial and Mesangial Proliferative Lupus Nephritis (ISN/RPS Class I and II)  Agnes B. Fogo, MD, Mark A. Lusco,
Dense Deposit Disease American Journal of Kidney Diseases
Volume 82, Issue 7, Pages (October 2012)
Volume 76, Issue 5, Pages (September 2009)
Cryoglobulinemic Glomerulopathy Complicating Helicobacter pylori–Associated Gastric Mucosa–Associated Lymphoid Tissue Lymphoma  Ammar Almehmi, MD, MPH,
Membranoproliferative Glomerulonephritis
AJKD Atlas of Renal Pathology: Fibrillary Glomerulonephritis
Glomerular disease related to anti-VEGF therapy
C3 Glomerulonephritis Associated With Complement Factor B Mutation
AJKD Atlas of Renal Pathology: Cryoglobulinemic Glomerulonephritis
An Uncommon Cause of Membranous Glomerulonephritis
Volume 77, Issue 9, Pages (May 2010)
Renal Manifestations of Inflammatory Bowel Disease
Volume 64, Issue 4, Pages (October 2003)
Donor kidney biopsies: pathology matters, and so does the pathologist
Volume 77, Issue 9, Pages (May 2010)
C3 glomerulopathy: consensus report
C3 glomerulopathy: what's in a name?
Postinfectious Glomerulonephritis
Lupus Nephritis: Mesangial and Membranous Forms (WHO II and V)
Erik H. Strøm, Michael J. Mihatsch  Kidney International 
Deposition of Complement Product C4d in Anti–Glomerular Basement Membrane Glomerulonephritis  Ibrahim Batal, MD, Geetha Chalasani, MD, Christine Wu, MD,
Lupus Nephritis: Proliferative Forms (WHO III, IV)
HIV-associated immune complex glomerulonephritis with “lupus-like” features: A clinicopathologic study of 14 cases1  Mark Haas, Sadhana Kaul, Joseph A.
Nephrotic Syndrome and a Maculopapular Rash
Volume 59, Issue 6, Pages (June 2001)
Toward a working definition of C3 glomerulopathy by immunofluorescence
AJKD Atlas of Renal Pathology: Proliferative Glomerulonephritis With Monoclonal Immunoglobulin Deposits  Mark A. Lusco, MD, Agnes B. Fogo, MD, Behzad.
Volume 88, Issue 4, Pages (October 2015)
Fibrillary Glomerulonephritis
AJKD Atlas of Renal Pathology: Membranous Nephropathy
Cryoglobulin-Related Glomerulonephritis
Volume 61, Issue 1, Pages (January 2002)
Volume 62, Issue 5, Pages (November 2002)
Acute Kidney Failure in the Third Trimester of Pregnancy
HIV-related nephropathy: A South African perspective
Volume 63, Issue 4, Pages (April 2003)
Hypertension, race, and glomeruli: more than simply a numbers game
Acute Kidney Injury and Proteinuria in a Patient With Diabetes and a Submandibular Mass  Prue Hill, MD, PhD, Prue Russell, MD, Christine Sammartino, MD,
C3 Glomerulonephritis: A Rare Etiology of the Pulmonary Renal Syndrome
Membranous-like glomerulopathy with masked IgG kappa deposits
Immunofluorescence on pronase-digested paraffin sections: A valuable salvage technique for renal biopsies  S.H. Nasr, S.J. Galgano, G.S. Markowitz, M.B.
AJKD Atlas of Renal Pathology: IgA Nephropathy
C1q Nephropathy American Journal of Kidney Diseases
Crescentic Glomerulonephritis Associated With Hypocomplementemic Urticarial Vasculitis Syndrome  Leah Balsam, MD, Mohammed Karim, MD, Frederick Miller,
IgA Nephropathy American Journal of Kidney Diseases
Membranous and crescentic glomerulonephritis in a patient with anti-nuclear and anti- neutrophil cytoplasmic antibodies  A. Chang, O. Aneziokoro, S.M.
Crescentic Glomerulonephritis With Ribbon-like Immunofluorescence Pattern  Venumadhav Chirunomula, MBBS, Venu Kondle, MD, Bhavani Vaddey, MBBS, Robert.
Volume 73, Issue 5, Pages (March 2008)
Agnes B. Fogo, MD, Mark A. Lusco, MD, Behzad Najafian, MD, Charles E
Volume 63, Issue 6, Pages (June 2003)
Quiz Page Answers May 2006 American Journal of Kidney Diseases
Volume 85, Issue 4, Pages (April 2014)
Collapsing glomerulopathy (CG) and lesions that may resemble CG histologically in renal biopsies from patients with systemic lupus erythematosus. Collapsing.
Cryoglobulinemic Glomerulopathy Complicating Helicobacter pylori–Associated Gastric Mucosa–Associated Lymphoid Tissue Lymphoma  Ammar Almehmi, MD, MPH,
IgA Nephropathy American Journal of Kidney Diseases
Volume 1, Issue 4, Pages (July 2019)
Dysproteinemia and the Kidney: Core Curriculum 2019
Presentation transcript:

Unmasking a unique glomerular lesion Christine VanBeek, Mark Haas  Kidney International  Volume 86, Issue 1, Pages 13-15 (July 2014) DOI: 10.1038/ki.2013.557 Copyright © 2014 International Society of Nephrology Terms and Conditions

Figure 1 Comparison of renal biopsy findings by light microscopy, immunofluorescence for C3, and electron microscopy in two cases of C3 glomerulopathy and one case of primary membranous glomerulopathy. (a, d, g) Light microscopy. (b, e, h) Immunofluorescence for C3. (c, f, i) Electron microscopy. In the case of membranous glomerulopathy (g–i), immunofluorescence for immunoglobulin G (IgG) and immunoperoxidase staining for phospholipase A2 receptor were positive with a pattern similar to that seen for C3 (h). In the two cases of C3 glomerulopathy (C3G) (a–f), there was minimal staining for IgG, IgA, or IgM. The light microscopic findings in all three cases, ranging from mesangial hypercellularity (a) to normocellular glomeruli (d, g), are all within the range of findings described in the cases of Larsen et al.3 (this issue), and all three cases show predominantly glomerular capillary wall staining for C3 by immunofluorescence, with similar, confluent granular staining patterns in one case of C3G (e) and the case of membranous glomerulopathy (h). By electron microscopy, one case of C3G (c) shows intramembranous and transmembranous deposits ranging from moderately electron-dense to largely electron-lucent, in a pattern similar to that described for membranoproliferative glomerulonephritis, type 3 of Strife and Anders.1 The deposits in the other case of C3G (f), while moderately electron-dense, are less well-defined and more segmental than those in the case of membranous glomerulopathy (i), with one deposit in the former case having a somewhat elongated appearance (f, glomerular basement membrane at right). (a, d, g) Periodic acid–Schiff stain; original magnification, × 400. (b, e, h) Immunofluorescence on fresh frozen tissue with fluorescein isothiocyanate-conjugated anti-human C3; original magnification, × 400. (c, f, i) Electron microscopy with uranyl acetate and lead citrate stain; original magnifications, × 7500 (c), × 14,000 (f), × 7200 (i). Kidney International 2014 86, 13-15DOI: (10.1038/ki.2013.557) Copyright © 2014 International Society of Nephrology Terms and Conditions