“…The occurrence of ANCA-associated NCGN and primary MGN in the same patient is rare, with only a handful of reports in the literature (5)(6)(7)(8)(9)(10). Herein, we detail the clinical, pathologic, and outcome data of 14 patients with this rare dual glomerulopathy and review the previously reported cases.…”
Conclusions: MGN with ANCA-associated NCGN is a rare dual glomerulopathy seen in patients with heavy proteinuria, acute renal failure, and active urine sediment. Prognosis is variable, with 50% of patients reaching endpoints of ESRD or death.
“…The occurrence of ANCA-associated NCGN and primary MGN in the same patient is rare, with only a handful of reports in the literature (5)(6)(7)(8)(9)(10). Herein, we detail the clinical, pathologic, and outcome data of 14 patients with this rare dual glomerulopathy and review the previously reported cases.…”
Conclusions: MGN with ANCA-associated NCGN is a rare dual glomerulopathy seen in patients with heavy proteinuria, acute renal failure, and active urine sediment. Prognosis is variable, with 50% of patients reaching endpoints of ESRD or death.
“…Coexistent MN and PNCGN is a rare occurrence, with only 25 reported cases in the English literature in which clinical and pathologic findings are detailed [9,[12][13][14][15][16][17][18]. Thirteen patients had P-ANCA by indirect immune fluorescent (IIF) staining, seven of whom were tested with ELISA and found to have MPO-ANCA.…”
Section: Discussionmentioning
confidence: 99%
“…Patients with both MN and PNCGN are likely to have heavier proteinuria than patients with PNCGN alone. All of 25 reported cases with urine output had proteinuria [9,[12][13][14][15][16][17][18]. From the recent report, the mean 24-h urine protein for these patients was 6.5 g, compared with 1.7 to 2.5 g in patients with ANCA disease alone [22].…”
Section: Discussionmentioning
confidence: 99%
“…Among the 25 reported cases of MN and PNCGN, induction therapy consisted of prednisone and CY in 20 patients, prednisone and azathioprine in one patient, and prednisone alone in one patient. One patient received mycophenolate mofetil and two patients also received plasmapheresis [9,[12][13][14][15][16][17][18].…”
Introduction: Membranous nephropathy (MN) is the most common causes of the nephrotic syndrome in nondiabetic, Caucasian adults. Pauci-immune necrotizing and crescentic glomerulonephritis (PNCGN) typically present with rapidly progressive glomerulonephritis. Coexistent MN and PNCGN is a rare occurrence. We report a case of both MPO-and PR3-ANCA associated NCGN with MN that presented as rapidly progressive glomerulonephritis.
“…A dual presentation of MPO-ANCA-associated glomerulonephritis with MN is rare [5][6][7][8][9][10][11]. We report here a rare case of MPO-ANCA-associated glomerulonephritis with MN suspected to be a secondary form.…”
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.