Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

suck abstract from ncbi


10.1159/000512330

http://scihub22266oqcxt.onion/10.1159/000512330
suck pdf from google scholar
33227797!?!33227797

suck abstract from ncbi

pmid33227797      Nephron 2020 ; 144 Suppl 1 (?): 43-48
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Recurrence of Proliferative Glomerulonephritis with Monoclonal Immunoglobulin G Deposits with a Striated Ultrastructure #MMPMID33227797
  • Namba-Hamano T; Hamano T; Imamura R; Yamaguchi Y; Kyo M; Yonishi H; Takahashi A; Kawamura M; Nakazawa S; Kato T; Abe T; Kyakuno M; Takabatake Y; Nonomura N; Isaka Y
  • Nephron 2020[]; 144 Suppl 1 (?): 43-48 PMID33227797show ga
  • A 64-year-old man with nephrotic syndrome was admitted to another hospital where his renal biopsy revealed membranoproliferative glomerulonephritis (MPGN) with monoclonal immunoglobulin (Ig) G, subclass 1, kappa light chain (IgG1kappa) deposition on immunofluorescence (IF). Proliferative glomerulonephritis with monoclonal IgG deposits (PGNMID) was suspected due to monoclonal IgG1kappa deposits and the absence of hematological abnormalities. However, the typical PGNMID phenotype was not observed by electron microscopy. Instead, an organized and striated muscle-like structure was observed in the subendothelial space. Since a 2-year treatment with immunosuppressants did not improve his proteinuria, a second biopsy was performed at our hospital. It showed an MPGN-like phenotype; however, monoclonal Ig deposits on IF were no longer observed. One year after the second biopsy, he developed ESRD. Thus, he underwent living kidney transplantation from his wife. Allograft biopsy was performed as proteinuria was observed 3 months after transplantation, which again showed an MPGN-like phenotype with monoclonal IgG1kappa deposits. The observed electron-dense deposits were similar to those in the native biopsies. Accordingly, the patient was diagnosed with recurrent MPGN. Adding methylprednisolone pulse therapy to conventional immunosuppressants did not improve the patient's renal function or proteinuria. He died of Legionella pneumonia 8 months after transplantation. Considering the patient's histological findings of MPGN with monoclonal IgG1kappa deposits and early recurrence of glomerulonephritis after transplantation, he was diagnosed with PGNMID with novel electron-dense deposits.
  • |Biopsy[MESH]
  • |Glomerulonephritis, Membranoproliferative/immunology/*pathology[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*analysis[MESH]
  • |Kidney Transplantation[MESH]
  • |Kidney/*ultrastructure[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]


  • DeepDyve
  • Pubget Overpricing
  • suck abstract from ncbi

    Linkout box