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Author Masani, Naveed N. ♦ D.’agati, Vivette D. ♦ Markowitz, Glen S.
Source CiteSeerX
Content type Text
File Format PDF
Subject Domain (in DDC) Computer science, information & general works ♦ Data processing & computer science
Subject Keyword Membranous Glomerulonephritis ♦ Indirect Immunofluorescence ♦ Acute Renal Failure ♦ Renal Function ♦ Heavy Proteinuria ♦ Anca-associated Ncgn ♦ Anca Positivity ♦ Antineutrophil Cytoplasmic Antibody ♦ Mean Follow-up ♦ Crescentic Glomerulonephritis ♦ Atypical Anca ♦ Pathologic Finding ♦ Concurrent Membranous Glomerulonephritis ♦ Ultrastructural Evaluation ♦ Rare Dual Glomerulopathy ♦ Follow-up Period ♦ Clinical Presentation ♦ Mg Dl ♦ Serum Creatinine ♦ Mean 24-hr Urine Protein ♦ Ii Membranous Change ♦ Active Urine Sediment ♦ Mean Age ♦ Mean Creatinine ♦ Rare Case ♦ Independent Predictor ♦ Pathologic Evaluation
Abstract Background and objectives: Only rare cases of concurrent membranous glomerulonephritis (MGN) and antineutrophil cytoplasmic antibody (ANCA)-associated necrotizing and crescentic glomerulonephritis (NCGN) have been reported. Design, setting, participants, & measurements: The authors report the clinical and pathologic findings in 14 patients with MGN and ANCA-associated NCGN. Results: The cohort consisted of eight men and six women with a mean age of 58.7 yr. ANCA positivity was documented by indirect immunofluorescence or ELISA in all patients. Indirect immunofluorescence was positive in 13 patients (seven P-ANCA, five C-ANCA, one atypical ANCA). ELISA was positive in nine of 10 patients (five MPO-ANCA, three PR3-ANCA, one MPO- and PR3-ANCA). Clinical presentation included heavy proteinuria (mean 24-hr urine protein 6.5 g/d), hematuria, and acute renal failure (mean creatinine 4.4 mg/dl). Pathologic evaluation revealed MGN and NCGN, with crescents involving a mean of 32 % of glomeruli. On ultrastructural evaluation, the majority of cases showed stage I or II membranous changes. Follow-up was available for 13 patients, 12 of whom were treated with steroids and cyclophosphamide. At a mean follow-up of 24.3 mo, five patients progressed to ESRD, seven had stabilization or improvement in renal function, and one had worsening renal function. Five patients, including three with ESRD, died during the follow-up period. The only independent predictor of progression to ESRD was serum creatinine at biopsy. 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.
Educational Role Student ♦ Teacher
Age Range above 22 year
Educational Use Research
Education Level UG and PG ♦ Career/Technical Study