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A Case of Nephrotic Syndrome With Minimal-Change Disease and Waldenstrom’s Macroglobulinemia
Author(s) -
Grabe
Publication year - 2013
Publication title -
journal of clinical medicine research
Language(s) - English
Resource type - Journals
eISSN - 1918-3011
pISSN - 1918-3003
DOI - 10.4021/jocmr1387w
Subject(s) - medicine , macroglobulinemia , proteinuria , waldenstrom macroglobulinemia , nephrotic syndrome , minimal change disease , paraproteins , prednisone , gastroenterology , gamma globulin , immunoelectrophoresis , renal biopsy , hypergammaglobulinemia , biopsy , immunology , kidney , disease , focal segmental glomerulosclerosis , antibody , multiple myeloma , lymphoma , monoclonal , monoclonal antibody
Kidney disease is a rare complication of Waldenstrom's macroglobulinemia. We report a case of nephrotic syndrome and minimal change disease in a patient with biopsy proven Waldenstrom's macroglobulinemia. The patient presented with over 12 grams of proteinuria and was successfully treated with oral prednisone over the course of 4 weeks. Repeat serum protein electrophoresis as well as serum immunoelectrophoresis revealed no paraproteins, urine analysis was negative for protein or blood by dipstick and spot urine protein was 9 mg/dL with creatinine of 101 mg/dL at time of last office visit. This case illustrates the successful treatment with corticosteroids alone with prolonged complete remission.

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