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Proliferative Glomerulonephritis With Monoclonal IgG3λ Deposits: A Case Report of a Rare Cause of Monoclonal Gammopathy of Renal Significance.
Yu, Xiao-Juan; Wang, Mang-Ju; Yong, Zi-Hao; Ma, Yi-Yi; Wang, Su-Xia; Zhou, Fu-de; Zhao, Ming-Hui.
Affiliation
  • Yu XJ; Renal Division, Department of Medicine, Peking University First Hospital, Beijing, PR China.
  • Wang MJ; Institute of Nephrology and Renal Pathology Center, Institute of Nephrology, Peking University, Beijing, PR China.
  • Yong ZH; Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, PR China.
  • Ma YY; Key Laboratory of CKD Prevention and Treatment, Ministry of Education of China, Beijing, PR China.
  • Wang SX; Department of Hematology, Peking University First Hospital, Beijing, PR China.
  • Zhou FD; Renal Division, Department of Medicine, Peking University First Hospital, Beijing, PR China.
  • Zhao MH; Institute of Nephrology and Renal Pathology Center, Institute of Nephrology, Peking University, Beijing, PR China.
Kidney Med ; 1(4): 221-225, 2019.
Article in En | MEDLINE | ID: mdl-32734203
ABSTRACT
Proliferative glomerulonephritis with monoclonal immunoglobulin G (IgG) deposits is a rare monoclonal gammopathy of renal significance with dense deposits on electron microscopy similar to polyclonal immune complex-mediated glomerulonephritis. 70% of patients with proliferative glomerulonephritis with monoclonal IgG are negative for a monoclonal (M) spike, and patients with this condition rarely develop an M spike during follow-up. We report a Chinese man in his 50s who presented with nephrotic syndrome and normal glomerular filtration rate. His first kidney biopsy showed masked IgG3 deposition, such that IgG3 staining was apparent only after digestion by enzyme on paraffin tissue, with a membranoproliferative pattern. During follow-up, his glomerular filtration rate worsened and proteinuria increased. 18 months after the first biopsy, the patient developed an M spike; a second kidney biopsy showed proliferative glomerulonephritis with monoclonal IgG deposits with unmasked IgG3λ deposition. The patient was successfully treated with bortezomib and dexamethasone, followed by lenalidomide and dexamethasone maintenance therapy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Kidney Med Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Kidney Med Year: 2019 Document type: Article