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10.1155/2014/164694

http://scihub22266oqcxt.onion/10.1155/2014/164694
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25136462!4129672!25136462
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suck abstract from ncbi

pmid25136462      Case+Rep+Nephrol 2014 ; 2014 (?): 164694
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  • Nephrotic syndrome secondary to proliferative glomerulonephritis with monoclonal immunoglobulin deposits of lambda light chain #MMPMID25136462
  • Yun S; Braunhut BL; Walker CN; Bhati W; Sussman AN; Anwer F
  • Case Rep Nephrol 2014[]; 2014 (?): 164694 PMID25136462show ga
  • We describe a rare case of a 46-year-old woman with history of refractory nephrotic syndrome and hypertension who presented with worsening proteinuria and kidney function. Work-up for both autoimmune and infectious diseases and hematologic malignancies including multiple myeloma were negative. Kidney biopsy demonstrated glomerular sclerotic change with lambda light chain deposits in the subendothelial space, which is consistent with proliferative glomerulonephritis with monoclonal immunoglobulin deposit (PGNMID). The patient was treated with bortezomib and dexamethasone without clinical improvement and eventually became hemodialysis dependent.
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