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10.1093/ckj/sfw032

http://scihub22266oqcxt.onion/10.1093/ckj/sfw032
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C4886922!4886922!27274823
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suck abstract from ncbi


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pmid27274823      Clin+Kidney+J 2016 ; 9 (3): 397-402
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  • Revisiting post-infectious glomerulonephritis in the emerging era of C3 glomerulopathy #MMPMID27274823
  • Khalighi MA; Wang S; Henriksen KJ; Bock M; Keswani M; Meehan SM; Chang A
  • Clin Kidney J 2016[Jun]; 9 (3): 397-402 PMID27274823show ga
  • Background: Post-infectious glomerulonephritis (PIGN) is an immune complex-mediated glomerular injury that typically resolves. Dominant C3 deposition is characteristic of PIGN, but with the emergence of C3 glomerulonephritis (C3GN) as a distinct entity, it is unclear how the pathologic similarities between PIGN and C3GN should be reconciled. Therefore, nephrologists and nephropathologists need additional guidance at the time of biopsy. Methods: We studied 23 pediatric and young adult patients diagnosed with PIGN. Patients were divided into two groups, one with co-dominance between C3 and immunoglobulins and the other meeting proposed diagnostic criteria for C3GN. Clinical and pathological features were compared. Results: No clinical and/or pathological features could distinguish between those with C3-co-dominant deposits and those with C3 dominance. Nearly all patients in both groups regained their baseline renal function without clinical intervention. Conclusions: Although the identification of abnormalities of the alternative pathway of complement is characteristic of C3GN, testing is not widely available and the turnaround time often exceeds 1 month. Our study found that PIGN with either co-dominant or dominant C3 deposition in a cohort of young patients has excellent short-term outcomes. Close clinical observation for persistent abnormalities, such as hypocomplementemia, prolonged hematuria or proteinuria, is recommended to single out patients that may harbor intrinsic complement abnormalities.
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