Membranous Glomerulonephritis With Crescents
نویسندگان
چکیده
منابع مشابه
Membranous nephropathy with crescents.
Membranous nephropathy is a common cause of nephrotic syndrome in adults and can be primary or secondary to systemic lupus erythematosus, chronic infection, or drugs. Rapid decline in renal function in patients with membranous nephropathy may be due to renal vein thrombosis, malignant hypertension, or an additional superimposed destructive process involving the renal parenchyma. Crescents are r...
متن کاملPost-infectious glomerulonephritis with crescents in adults: a retrospective study
BACKGROUND Crescent formation generally reflects severe glomerular injury. There is sparse literature on post-infectious glomerulonephritis (PIGN) with crescents in adults. This retrospective study looked at nine such cases to see if there is a correlation between the severity of presentation, steroid treatment, histological severity and outcome. METHODS Biopsy reports of all the adults who u...
متن کاملMembranous glomerulonephritis with ANCA-associated necrotizing and crescentic glomerulonephritis.
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...
متن کاملMembranous glomerulonephritis associated with ulcerative colitis.
Glomerulonephritis is reported as a rare extraintestinal manifestation of inflammatory bowel disease. We report a case of a 69-year-old woman who suffered from membranous glomerulonephritis, 3 years after diagnosis of nephrotic syndrome. She was admitted because of acute kidney failure, bloody diarrhea, and gastrointestinal symptoms. Further evaluation confirmed the diagnosis of ulcerative coli...
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ژورنال
عنوان ژورنال: Kidney International Reports
سال: 2019
ISSN: 2468-0249
DOI: 10.1016/j.ekir.2019.07.021