Literature DB >> 11328533

Glomerular crescents in renal amyloidosis: an epiphenomenon or distinct pathology?

M Nagata1, T Shimokama, A Harada, A Koyama, T Watanabe.   

Abstract

There have been several reports of cases of renal amyloidosis with glomerular crescents. However, it is not clear whether the association is fortuitous or pathogenic related. The present study analyzed 105 cases of renal amyloidosis (61 autopsy cases and 44 biopsy cases) and found glomerular crescents in 14 (13.3%) cases. Among the 14 cases with crescents, a female predominance was noted (male: female, 3: 11) and rheumatoid arthritis was the most common primary disease of amyloidosis. Immunohistochemical analysis demonstrated amyloid protein of AA type in 12 cases. According to the histologic classification, there were 11 cases of mesangial nodular type, which was almost exclusively accompanied by AA amyloid deposition. Of note, the incidence of crescents neither correlated with the extent of amyloid deposition nor the presence of nephrotic syndrome. By contrast, localization of amyloid deposition was closely related to crescent formation. Moreover, electron microscopic observation displayed rupture of the glomerular basement membrane at the site of amyloid deposition. Our results indicated that glomerular crescents were more frequently associated with renal amyloidosis than previously appreciated. Rupture of the fragile glomerular basement membrane by amyloid deposition, as revealed by immunostaining and electron microscopy, may be the mechanism of crescent formation. We suggest that glomerular crescents are a distinct pathology associated with renal amyloidosis, not fortuitous conditions.

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Year:  2001        PMID: 11328533     DOI: 10.1046/j.1440-1827.2001.01188.x

Source DB:  PubMed          Journal:  Pathol Int        ISSN: 1320-5463            Impact factor:   2.534


  8 in total

1.  Tocilizumab-induced remission of nephrotic syndrome accompanied by secondary amyloidosis and glomerulonephritis in a patient with rheumatoid arthritis.

Authors:  Shunsuke Yamada; Akihiro Tsuchimoto; Yoshiki Kaizu; Masatomo Taniguchi; Kosuke Masutani; Hiroshi Tsukamoto; Hiroaki Ooboshi; Kazuhiko Tsuruya; Takanari Kitazono
Journal:  CEN Case Rep       Date:  2014-07-29

2.  Sarcoidosis-associated renal AA amyloidosis and crescentic necrotizing glomerulonephritis.

Authors:  Albert Bui; Cherise Cortese; Nabeel Aslam
Journal:  Proc (Bayl Univ Med Cent)       Date:  2022-05-16

3.  Cancer-Associated AA Amyloidosis Presenting as Crescentic Glomerulonephritis.

Authors:  Jonathan E Zuckerman; Fenghua Peng; Bethany E Karl; Carl E Schulze; Anthony Sisk
Journal:  Kidney Int Rep       Date:  2019-03-04

Review 4.  Serum Amyloid A Protein-Associated Kidney Disease: Presentation, Diagnosis, and Management.

Authors:  Jordan Thorne; David Clark; Laurette Geldenhuys; Keigan More; Amanda Vinson; Karthik Tennankore
Journal:  Kidney Med       Date:  2022-06-26

5.  Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis with Kidney Involvement in a Patient with AL Amyloidosis.

Authors:  Brendan L Thoms; Varun Agrawal; Elvira R Umyarova; Pamela C Gibson; Richard J Solomon
Journal:  Case Rep Nephrol Dial       Date:  2021-07-08

6.  Rapidly progressive glomerulonephritis in a patient with renal amyloidosis: Case report and review of the literature.

Authors:  Y J Anupama; M Vankalakunti
Journal:  Indian J Nephrol       Date:  2012-09

7.  Rapidly progressive glomerulonephritis due to coexistent anti-glomerular basement membrane disease and fibrillary glomerulonephritis.

Authors:  Wisit Cheungpasitporn; Claudia C Zacharek; Fernando C Fervenza; Lynn D Cornell; Sanjeev Sethi; Loren P Herrera Hernandez; Samih H Nasr; Mariam P Alexander
Journal:  Clin Kidney J       Date:  2015-11-30

8.  Revisiting renal amyloidosis with clinicopathological characteristics, grading, and scoring: A single-institutional experience.

Authors:  Abhiram Kalle; Archana Gudipati; Sree Bhushan Raju; Karthik Kalidindi; Swarnalatha Guditi; Gangadhar Taduri; Megha S Uppin
Journal:  J Lab Physicians       Date:  2018 Apr-Jun
  8 in total

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