scholarly journals Unusual case of stable dense deposit disease over 20 years

2016 ◽  
Vol 3 (3) ◽  
pp. 57
Author(s):  
Satyanarayana R Vaidya ◽  
Chandana R Bhavanam ◽  
Ananda R Gurram

Dense deposit disease (DDD) is a prototypical form of C3 Glomerulopathy that affects both children and adults at a rate of 2 to 3 people per million. It often progresses to ESRD and recurs after Renal Transplantation. DDD presentation for 10 years or more is known to progress to ESRD in half of patients. We report a rare case of DDD which has been in clinical and histological remission for 14 years after treatment with Glucocorticoid therapy.

2014 ◽  
Vol 29 (10) ◽  
pp. 2055-2059 ◽  
Author(s):  
Ana Sánchez-Moreno ◽  
Francisco De la Cerda ◽  
Rocío Cabrera ◽  
Julia Fijo ◽  
Margarita López-Trascasa ◽  
...  

2014 ◽  
Vol 173 (6) ◽  
pp. 767-772 ◽  
Author(s):  
Julianne Prasto ◽  
Bernard S. Kaplan ◽  
Pierre Russo ◽  
Elaine Chan ◽  
Richard J. Smith ◽  
...  

2013 ◽  
Vol 33 (6) ◽  
pp. 493-507 ◽  
Author(s):  
Thomas D. Barbour ◽  
Matthew C. Pickering ◽  
H. Terence Cook

2019 ◽  
Vol 8 (3) ◽  
pp. 30-30
Author(s):  
Sofia Semedo Coelho ◽  
Ana Raquel Fernandes ◽  
Elsa Soares ◽  
Patrícia Valério ◽  
Bruno Matos ◽  
...  

Background: C3 glomerulopathy is a recently described entity classified as complementassociated glomerular disease. Case Presentation: We report a case of a 48-year-old man referred to the nephrology department for nephrotic syndrome with rapidly progressive kidney failure, acquired partial lipodystrophy and drusen in Bruch’s membrane of the retina. Blood tests showed low C3 and no evidence for autoimmune diseases, monoclonal gammopathy or infection. The renal biopsy revealed a proliferative endocapillary and crescentic glomerulonephritis with glomerular deposits exclusively of C3 and significant interstitial fibrosis. The electronic microscopy was consistent with dense deposit disease. The complement analysis revealed a pathogenic mutation of the complement factor B (CFB) gene not previously described in literature. Conclusions: The authors report a new mutation of CFB, in a dense deposit disease patient; this finding brings a new insight to the pathogenic pathway of C3 glomerulopathy and possibly to other complement dysregulation associated glomerular diseases. More clinical trials are needed to clarify both the pathogenicity and the optimal treatment for these entities.


2018 ◽  
Vol 5 (1) ◽  
pp. 41
Author(s):  
Mritunjay Kumar ◽  
Alok Sharma ◽  
Sandipan Sirkar ◽  
Aditya Saun

2006 ◽  
Vol 56 (2) ◽  
pp. 101-109 ◽  
Author(s):  
Kumi Aita ◽  
Shinichi Ito ◽  
Kazunari Tanabe ◽  
Hiroshi Toma ◽  
Yutaka Yamaguchi ◽  
...  

2020 ◽  
Vol 15 (9) ◽  
pp. 1287-1298 ◽  
Author(s):  
Fernando Caravaca-Fontán ◽  
Montserrat M. Díaz-Encarnación ◽  
Laura Lucientes ◽  
Teresa Cavero ◽  
Virginia Cabello ◽  
...  

Background and objectivesC3 glomerulopathy is a complement-mediated disease arising from abnormalities in complement genes and/or antibodies against complement components. Previous studies showed that treatment with corticosteroids plus mycophenolate mofetil (MMF) was associated with improved outcomes, although the genetic profile of these patients was not systematically analyzed. This study aims to analyze the main determinants of disease progression and response to this therapeutic regimen.Design, setting, participants, & measurements We conducted a retrospective, multicenter, observational cohort study in 35 nephrology departments belonging to the Spanish Group for the Study of Glomerular Diseases. Patients diagnosed with C3 glomerulopathy (n=81) or dense deposit disease (n=16) between January 1995 and March 2018 were enrolled. Multivariable and propensity score matching analyses were used to evaluate the association of clinical and genetic factors with response to treatment with corticosteroids and MMF as measured by proportion of patients with disease remission and kidney survival (status free of kidney failure).ResultsThe study group comprised 97 patients (84% C3 glomerulopathy, 16% dense deposit disease). Forty-two patients were treated with corticosteroids plus MMF, and this treatment was associated with a higher rate of remission and lower probability of kidney failure (79% and 14%, respectively) compared with patients treated with other immunosuppressives (24% and 59%, respectively), or ecluzimab (33% and 67%, respectively), or conservative management (18% and 65%, respectively). The therapeutic superiority of corticosteroids plus MMF was observed both in patients with complement abnormalities and with autoantibodies. However, patients with pathogenic variants in complement genes only achieved partial remission, whereas complete remissions were common among patients with autoantibody-mediated forms. The main determinant of no remission was baseline proteinuria. Relapses occurred after treatment discontinuation in 33% of the patients who had achieved remission with corticosteroids plus MMF, and a longer treatment length of MMF was associated with a lower risk of relapse.ConclusionsThe beneficial response to corticosteroids plus MMF treatment in C3 glomerulopathy appears independent of the pathogenic drivers analyzed in this study.


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