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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom